Erythema Gyratum Repens, another cutaneous marker of malignancy. ??
Eritema Gyratum Repens, otro marcador cutaneo de malignidad.??
EDITORIAL ENGLISH
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Hello friends of the network, DERMAGIC again with ANOTHER CUTANEOUS SIGN of MALIGNANCY in most cases. THE ERYTHEMA GYRATUM REPENS or The GAMMEL syndrome. For the first time described in the year 1.952 by GAMMEL in a female patient of 55 years with breast cancer with axillary invasion, the cutaneous sign appeared 9 months before the malignancy and disappeared 10 days after the surgery.
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Hello friends of the network, DERMAGIC again with ANOTHER CUTANEOUS SIGN of MALIGNANCY in most cases. THE ERYTHEMA GYRATUM REPENS or The GAMMEL syndrome. For the first time described in the year 1.952 by GAMMEL in a female patient of 55 years with breast cancer with axillary invasion, the cutaneous sign appeared 9 months before the malignancy and disappeared 10 days after the surgery.
In 1.975 SKOLNICK and MAIMAN reviewed the literature and found 31 cases of
ERYTHEMA GYRATUM REPENS, all of them ASSOCIATED WITH MALIGNANCY, by that
date only 3 cases NOT ASSOCIATED WITH MALIGNANCY had been reported.
By the year 1.985, 28 cases of ERYTHEMA GYRATUM REPENS had been reported,
of which 24 (85%) were associated with malignancy. In 15 cases (68%) the
CUTANEOUS SIGN was present before the malignancy, in 6 cases (27%) it
appeared after the malignancy was detected, and in 1 case (4%) it appeared
at the same time as the malignancy.
By the year 1.995, 60 cases of ERYTHEMA GYRATUM REPENS had been described,
of which 46 (77%) were associated with malignancy. And 14 cases (23%) not
associated with malignancy.
In recent years, rashes have been described "LIKE" to ERYTHEMA GYRATUM
REPENS in different pathologies, type EGR-like eruption.
By the year 2.012 One hundred twelve original cases of EGR were selected
from the literature for detailed review. Among these, 58 cases (70%) were
associated with an underlying neoplasm, 25 non-paraneoplastic cases, and 29
cases were considered as different dermatoses simulating EGR in its clinical
presentation (EGR-like eruption).
Based on these findings, we can classify the ERYTHEMA GYRATUM REPENS in
three variants: ASSOCIATED WITH MALIGNITY, in most cases, and the minority
is NOT ASSOCIATED with MALIGNANCY. And another VARIANT: CUTANEOUS ERUPTIONS
MIMICKING (LIKE) ERITEMA GYRATUM REPENS.
A.) MALIGNITIES ASSOCIATED WITH ERITEMA GIRATUM REPENS:
1.) LUNG.
1.) LUNG.
2.) ESOPHAGUS.
3.) BREAST.
4.) UTERUS.
5.) PHARYNX.
6.) STOMACH.
7.) ANUS.
8.) BLADDER.
9.) INTESTINE.
10.) HODGKINS DISEASE
11.) TONGUE.
12.) PROSTATE.
13.) PANCREAS.
14.) MYELOMA.
15.) METASTASIS
B.) ERITEMA GIRATUM REPENS NOT ASSOCIATED WITH MALIGNANCY:
1.) ICHTHYOSIS.
2.) PALMAR AND PLANTAR HYPERKERATOSI.
3. PITYRIASIS RUBRA PILARIS.
4.) PSORIASIFORM LESIONS.
5.) BULLOUS PEMPHIGOID.
6.) PEMPHIGUS VULGARIS.
7.) BULLAE DISEASES.
8.) DISCOID LUPUS ERYTHEMATOSUS.
9.) PNEUMONIA..
10.) RHEUMATOID ARTHRITIS.
11.) HEALTHY PEOPLE.
12.) BREAST HYPERTROPHY.
13.) TUBERCULOSIS.
14.) HYPEREOSINOPHILIC SYNDROME.
C.) ERITEMA GIRATUM REPENS-LIKE ERUPTIONS:
1.) LEPROSY.
2.) LEUCOCYTHOCLASTIC VASCULITIS.
3.) URTICARIAL VASCULITIS.
4.) PSORIASIS.
5.) EPIDERMOLYSIS BULLOSA ACQUISITA.
6.) MYCOSIS FUNGOIDES.
7.) ERYTHROKERATODERMIA VARIABILIS.
8.) SJOGREN SYNDROME.
9.) SYSTEMIC LUPUS ERYTHEMATOSUS.
10.) DRUGS (PENICILLIN).
" ...The pattern of EGR has been described as
wood-grained,serpiginous, zebralike, cypress rings gyrate,
whorled,and swirls of rope. The expanding borders are usually
macular but may occasionally be palpable Scale is usually present. The
eruption of EGR moves rapidly across the surface of the skin, usually
about 1 cm per day...."
So friends and colleagues dermatologists, if you find this CUTANEOUS SIGN in any of your patients, check yourself with this bibliographic review and perform the appropriate tests, mainly rule out MALIGNANCY, but remember that a Lower percentage is not associated with it.
In the 70 references the facts, in the attach, clasic ERYTEMA GYRATUM
REPENS
Greetings to all.
Dr Jose Lapenta.
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EDITORIAL ESPAÑOL
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Hola amigos de la red DERMAGIC de nuevo con ustedes OTRO SIGNO CUTANEO marcador de MALIGNIDAD en la mayoria de los casos. EL ERITEMA GYRATUM REPENS O sindrome de GAMMEL. Por primera vez descrito en el año de 1.952 por GAMMEL en una paciente femenina de 55 años con cancer de seno con invasion axilar, el signo cutaneo aparecio 9 meses antes de la malignidad y desaparecio 10 dias despues de la cirugia.
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Hola amigos de la red DERMAGIC de nuevo con ustedes OTRO SIGNO CUTANEO marcador de MALIGNIDAD en la mayoria de los casos. EL ERITEMA GYRATUM REPENS O sindrome de GAMMEL. Por primera vez descrito en el año de 1.952 por GAMMEL en una paciente femenina de 55 años con cancer de seno con invasion axilar, el signo cutaneo aparecio 9 meses antes de la malignidad y desaparecio 10 dias despues de la cirugia.
En el año de 1.975 SKOLNICK y MAIMAN revisaron la literatura y
encontraron 31 casos de ERITEMA GYRATUM REPENS, todos ASOCIADOS A
MALIGNIDAD, para esa fecha solo se habian reportado 3 casos NO ASOCIADOS A
MALIGNIDAD.
Para el año de 1.985 se habian reportado 28 casos de ERITEMA GIRATUM
REPENS, de los cuales 24 (85%) estaban asociados a malignidad. En 15 de
los casos (68%) el SIGNO CUTANEO se presento antes que la malignidad, en 6
casos (27%) aparecio luego de detactada la malignidad, y en 1 caso (4 %)
aparecio al mismo tiempo que la malignidad.
Para el año de 1.995 se habian descrito 60 casos de ERITEMA GIRATUM
REPENS, de los cuales 46 (77%) estuvo asociado a malignidad. y 14
casos(23%) no asociado a malignidad.
En los ultimos años se han descrito erupciones cutaneas "similares al
ERITEMA GYRATUM REPENS en diferentes patologias, tipo LIKE-EGR.
Para el año 2.012 Ciento doce casos originales de EGR fueron
seleccionados de la literatura para su revisión detallada. Entre estos, 58
casos (70%) se asociaron con una neoplasia subyacente, 25 casos (30%) no
paraneoplásicos y 29 casos fueron considerados como diferentes dermatosis
simulando EGR en su presentación clínica (erupción tipo EGR).
En base a estos hallazgos podemos clasificar al ERITEMA GYRATUM REPENS en
TRES variantes: ASOCIADO A MALIGNIDAD, en la mayoria de los casos, Y NO
ASOCIADO A MALIGNIDAD la minoria. y otra VARIANTE: ERUPCIONES CUTANEAS QUE
SIMULAN al ERITEMA GIRATUM REPENS.
A.) MALIGNIDADES ASOCIADAS AL ERITEMA GIRATUM REPENS:
1.) PULMON.
2.) ESOFAGO.
3.) SENOS.
4.) UTERO.
5.) FARINGE.
6.) ESTOMAGO.
7.) ANO.
8.) VEJIGA.
9.) INTESTINO.
10.) ENFERMEDAD DE HODGKINS
11.) LENGUA.
12.) PROSTATA.
13.) PANCREAS.
14.) MIELOMA.
15.) METASTASIS
B.) ERITEMA GIRATUM REPENS NO ASOCIADO A MALIGNIDAD:
1.) ICTIOSIS.
2.) HIPERQUERATOSIS PALMO PLANTAR.
3.) PITIRIASIS RUBRA PILAR.
4.) LESIONES PSORIASIFORMES.
5.) PENFIGOIDE BULOSO.
6.) PENFIGO VULGAR.
7.) ENFERMEDADES AMPOLLARES.
8.) LUPUS ERITEMATOSOS DISCOIDEO CRONICO.
9.) NUEMONIA.
10.) ARTRITIS REUMATOIDE.
11.) PERSONAS SANAS.
12.) HIPERTROFIA MAMARIA.
13.) TUBERCULOSIS.
14.) SINDROME HIPEREOSINOFILICO.
C.) ERITEMA GIRATUM REPENS-LIKE ERUPCIONES:
1.) LEPRA.
2.) VASCULITIS LEUOCITOCLASTICA.
3.) VASCULITIS URTICARIANA.
4.) PSORIASIS.
5.) EPIDERMOLISIS BULOSA ADQUIRIDA.
6.) MICOSIS FUNGOIDES.
7.) ERITROQUERATODERMIA VARIABILIS.
8.) SINDROME DE SJOGREN.
9.) LUPUS ERITEMATOSOS SISTEMICO.
10.) DROGAS (PENICILINA).
"...El patrón de EGR se ha descrito como disposicion de anillos
longitudinales tipo "madera-veteada" serpiginoso, cebra-like, anillos de
ciprés, y Remolinos de cuerda. Los bordes de expansión suelen ser
maculares pero ocasionalmente puede ser palpable, la descamacion está
generalmente presente. La erupción de EGR. Se mueve rápidamente a través
de la superficie de la piel, usualmente alrededor de 1 cm por
día...."
De modo amigos y colegas dermatologos, si se te presenta este SIGNO
CUTANEO en alguno de sus pacientes, orientate con esta revision
bibliografica y realiza los examenes adecuados, principalmente descartar
MALIGNIDAD, pero recordemos que un porcentaje menor no esta asociado a
ella.
En las 70 referencias los hechos, en el adjunto: ERITEMA GYRATUM REPENS
CLASICO.
Saludos a todos.
Dr Jose Lapenta.
51.) Cutaneous manifestations of lung cancer.
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Owen CE1.
Author information
1University of Louisville, Division of Dermatology, Louisville, KY. Electronic address: ceowen01@louisville.edu.
Abstract
Skin findings can serve as a clue to internal disease. In this article, cutaneous manifestations of underlying lung malignancy are reviewed. Paraneoplastic dermatoses are rare, but when recognized early, can lead to early diagnosis of an underlying neoplasm. Malignancy-associated dermatoses comprise a broad group of hyperproliferative and inflammatory disorders, disorders caused by tumor production of hormonal or metabolic factors, autoimmune connective tissue diseases, among others. In this review, paraneoplastic syndromes associated with lung malignancy are discussed, including ectopic ACTH syndrome, bronchial carcinoid variant syndrome, secondary hypertrophic osteoarthropathy/digital clubbing, erythema gyratum repens, malignant acanthosis nigricans, sign of Leser-Trélat, tripe palms, hypertrichosis lanuginosa, acrokeratosis paraneoplastica, and dermatomyositis.
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52.) Cutaneous manifestations of breast cancer.
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Semin Oncol. 2016 Jun;43(3):331-4. doi: 10.1053/j.seminoncol.2016.02.030. Epub 2016 Feb 23.
Tan AR1.
Author information
1Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC. Electronic address: Antoinette.Tan@CarolinasHealthcare.org.
Abstract
Breast cancer may present with cutaneous symptoms. The skin manifestations of breast cancer are varied. Some of the more common clinical presentations of metastatic cutaneous lesions from breast cancer will be described. Paraneoplastic cutaneous dermatoses have been reported as markers of breast malignancy and include erythema gyratum repens, acquired ichthyosis, dermatomyositis, multicentric reticulohistiocytosis, and hypertrichosis lanuginosa acquisita. Mammary Paget's disease, often associated with an underlying breast cancer, and Cowden syndrome, which has an increased risk of breast malignancy, each have specific dermatologic findings. Recognition of these distinct cutaneous signs is important in the investigation of either newly diagnosed or recurrent breast cancer.
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53.) Erythema gyratum repens.
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Eubanks LE1, McBurney E, Reed R.
Author information
1Department of Dermatology, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Abstract
BACKGROUND:
Erythema gyratum repens is a rare, clinically specific, and distinctive paraneoplastic syndrome. It is associated with internal malignancy in 82% of patients.
OBJECTIVE:
A 58-year-old man with erythema gyratum repens is described. On diagnosis of his eruption, a malignancy work-up revealed a 9-mm pulmonary adenocarcinoma. Removal of the carcinoma resulted in clearing of the erythema.
RESULTS:
Erythema gyratum repens is most commonly associated with bronchial, esophageal, and breast cancer. It has also rarely been reported in patients without evidence of malignancy. The histopathologic findings are nonspecific. Direct immunofluorescence has sometimes revealed C3, C4, or immunoglobulin G at the basement membrane zone.
CONCLUSION:
The etiology of erythema gyratum repens is unknown, although an immune response is postulated. Treatment involves treating the underlying malignancy.
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54.) Erythema gyratum repens unassociated with underlying malignancy.
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J Dermatol. 1995 Aug;22(8):587-9.
Kawakami T1, Saito R.
Author information
1Second Department of Dermatology, Toho University School of Medicine, Tokyo, Japan.
Abstract
A case of erythema gyratum repens occurring in a 62-year-old woman is presented together with a review of the literature. Evaluation and follow-up for the development of malignancy over a 32-month period failed to reveal any evidence of malignancy. Formerly, all cases of erythema gyratum repens were evaluated in terms of an association with an underlying malignant disorder. To date, only sixty cases have been reported in the literature; 14 (23%) were not found to be associated with any neoplasm. Therefore, this term is now also used for cases unassociated with malignancy. Erythema gyratum repens is a cutaneous eruption with a characteristic diagnostic morphology resembling a wood grain pattern.
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55.) Erythema gyratum repens unassociated with internal malignancy.
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J Am Acad Dermatol. 1985 May;12(5 Pt 2):911-3.
Langlois JC, Shaw JM, Odland GF.
Abstract
A case report of erythema gyratum repens occurring in a 68-year-old man is presented. Evaluation and follow-up for development of malignancy over a 39-month period failed to reveal evidence of malignancy. The patient died of an unrelated cause. Autopsy did not demonstrate any evidence of malignancy.
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56.) Erythema gyratum repens associated with cryptogenic organizing pneumonia.
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Indian J Dermatol Venereol Leprol. 2016 Mar-Apr;82(2):212-3. doi: 10.4103/0378-6323.173594.
Samotij D, Szczech J, Bencal-Kusinska M, Reich A1.
Author information
1Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Wroclaw, Poland.
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57.) Erythema gyratum repens preceding the onset of rheumatoid arthritis.
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Eur J Dermatol. 2013 May-Jun;23(3):399-400. doi: 10.1684/ejd.2013.2049.
Endo Y1, Fujisawa A1, Tanioka M1, Miyachi Y1.
Author information
1Department of Dermatology, Kyoto University, 54 Shogoin-Kawara-cho, Sakyo, Kyoto 606-8507, Japan.
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58.) Erythema gyratum repens associated with hypereosinophilic syndrome.
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J Dermatol. 1994 Aug;21(8):612-4.
Morita A1, Sakakibara N, Tsuji T.
Author information
Abstract
We report a case of typical erythema gyratum repens lesions observed as a manifestation of idiopathic hypereosinophilic syndrome in a 63-year-old man. While erythema gyratum repens is usually associated with malignancy, an intensive search over a 30-month period failed to reveal any evidence of neoplasm. With administration of dapsone, the typical gyrate lesions disappeared as the subject's hypereosinophilia improved.
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59.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
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Med Cutan Ibero Lat Am. 1983;11(4):281-6.
[Article in Spanish]
Yebra Sotillo I, Garciá Bravo B, Camacho Martínez F.
Abstract
A 65 year old male with Hodgkins disease, and generalised figurate Erythema, which during his period of hospitalisation migrated and became much more evident, disappearing after initial therapy. Diagnosed as "Erythema gyratum repens" reported by Gammel, an uncommon form of paraneoplasic migrant figurate Erythema, we review the 33 previous cases of this process, and find that, although 30 were related to other processes.
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60.) Erythema gyratum repens is not an obligate paraneoplastic disease: a systematic review of the literature and personal experience.
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J Eur Acad Dermatol Venereol. 2014 Jan;28(1):112-5. doi: 10.1111/j.1468-3083.2012.04663.x. Epub 2012 Jul 25.
Rongioletti F1, Fausti V, Parodi A.
Author information
1Section of Dermatology, DISSAL, University of Genoa, Genoa, Italy.
Abstract
BACKGROUND:
Erythema gyratum repens (EGR) is a rare clinical entity that is considered to be an obligatory paraneoplastic disease. According to the literature, an underlying neoplasm can be detected in 82% of the cases.
OBJECTIVES:
The aim of this systemic review was to evaluate the association of EGR with malignancies or other non-neoplastic conditions.
METHODS:
The medical records of patients seen at the Section of Dermatology, University of Genoa between 1990 and 2010, in whom a diagnosis of EGR had been made, were reviewed for evidence of systemic associations. A systematic search of the Cochrane library, EMBASE, Pubmed and MEDLINE databases was also conducted. Key search term used in the review was 'erythema gyratum repens'.
RESULTS:
Four patients with a diagnosis of EGR have been retrieved from our medical records. One case was idiopathic, one was associated with a bronchial carcinoma and two were associated with drug-intake. One hundred and twelve original cases of EGR were selected from the literature for detailed review. Among these, 58 cases (70%) were associated with an underlying neoplasm, 25 cases (30%) were non-paraneoplastic and 29 cases have been considered as different dermatoses mimicking EGR in their clinical presentation ('EGR-like' eruption).
CONCLUSION:
EGR should no longer be considered as an obligate paraneoplastic syndrome as the cases that are not associated with neoplasm are more than expected. In addition to searching an underlying neoplasm, dermatologists should be aware about the possibility of other associations including also drug-intake.
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61.) Novel presentation of lepromatous leprosy in an erythema gyratum repens-like pattern.
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Int J Dermatol. 2014 Feb;53(2):210-2. doi: 10.1111/ijd.12237. Epub 2013 Dec 10.
Mohanan S1, Devi AS, Kumari R, Thappa DM, Ganesh RN.
Author information
1Department of Skin and Sexually Transmitted Diseases, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Abstract
OBJECTIVES:
Leprosy can have diverse cutaneous and occasionally perplexing presentations. We report an unusual case of lepromatous leprosy (LL) with annular lesions resembling erythema gyratum repens.
REPORT:
A 55-year-old man presented with a symmetrical, hypopigmented, and erythematous rash of bizarre appearance over the lateral aspect of the upper arm, and anterior and posterior aspects of the trunk of two months' duration. He gave a history of self-resolving episodes of bilateral pedal edema, and numbness and pricking sensations in both the hands and feet, which had occurred intermittently over the previous six years. An ulcer measuring 2 cm in size was present over the adjacent surface of the right first and second toes. The bilateral ulnar and radial cutaneous nerves were symmetrically thickened.
RESULTS:
Slit-skin smears revealed numerous acid-fast bacilli. Skin biopsy from the trunk showed collections of histiocytes, lymphocytes, and plasma cells in the dermis and around the blood vessels. The patient was diagnosed with LL and started on multibacillary multi-drug therapy.
CONCLUSIONS:
Lepromatous leprosy can have varied clinical manifestations and is often a great imitator. However, the skin smear positivity, even in normal skin, symmetrical cutaneous and peripheral nerve involvement, and histopathology in the present patient were indicative of LL. This report highlights a rare presentation of leprosy. Clinicians should be aware of these rare manifestations as lepromatous cases still occur in certain regions.
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62.) Leucocytoclastic vasculitis presenting as an erythema gyratum repens-like eruption.
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Clin Exp Dermatol. 2016 Apr;41(3):320-2. doi: 10.1111/ced.12749. Epub 2015 Sep 3.
Spierings NM1, Natkunarajah J2.
Author information
1Dermatology Department, Ground Floor, Lanesborough Wing, St. George's Hospital NHS Trust, Blackshaw Road, London, SW17 0QT, UK. nspierings@doctors.org.uk.
2Dermatology Department, Kingston Hospital NHS Trust, London, UK.
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63.) Urticarial vasculitis presenting as erythema gyratum repens-like eruption.
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Noda S, Takekoshi T, Tamaki Z, Asano Y, Sugaya M, Sato S.
J Eur Acad Dermatol Venereol. 2011 Apr;25(4):493-5. doi: 10.1111/j.1468-3083.2010.03747.x.
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64.) Erythema gyratum repens-like eruption occuring in resolving psoriasis during methotrexate therapy.
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Int J Dermatol. 2010 Mar;49(3):306-7. doi: 10.1111/j.1365-4632.2009.04256.x.
Singal A1, Sonthalia S, Pandhi D.
Author information
1Department of Dermatology and STD, University College of Medical Sciences and GTB Hospital, University of Delhi, New Delhi, India.
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65.) Erythema gyratum repens-like eruption in a patient with epidermolysis bullosa acquisita
associated with ulcerative colitis.
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Br J Dermatol. 2007 Apr;156(4):773-5. Epub 2007 Jan 30.
España A, Sitaru C, Pretel M, Aguado L, Jimenez J.
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66.) Erythema gyratum repens-like eruption in mycosis fungoides: is dermatophyte superinfection
underdiagnosed in cutaneous T-cell lymphomas?
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J Eur Acad Dermatol Venereol. 2008 Nov;22(10):1276-8. doi: 10.1111/j.1468-3083.2008.02628.x. Epub 2008 Mar 7.
Jouary T, Lalanne N, Stanislas S, Vergier B, Delaunay M, Taieb A.
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67.) Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.
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Landau M1, Cohen-Bar-Dayan M, Hohl D, Ophir J, Wolf CR, Gat A, Mevorah B.
Author information
1Dermatology Unit, Edith Wolfson Medical Center, Holon, Israel, Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel. landau@post.tau.ac.il
Abstract
A large pedigree with erythrokeratodermia variabilis (EKV) and erythema gyratum repens-like lesions is described. Clinical, laboratory, and histologic findings of this family are presented. The differential diagnoses of the following dermatoses with an erythematous and a hyperkeratotic component are discussed: erythrokeratodermia variabilis (Mendes da Costa), progressive symmetric erythrokeratoderma (Gottron), loricrin keratoderma, erythrokeratoderma en cocardes (Degos), Netherton syndrome, keratitis-ichthyosis-deafness (KID) syndrome, erythrokeratolysis hiemalis (Oudtshoorn disease), and nonbullous congenital ichthyosiform erythroderma.
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68.) Erythema gyratum repens-like eruption in a patient with Sjögren syndrome.
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Acta Derm Venereol. 1995 Jul;75(4):327.
Matsumura T, Kumakiri M, Sato-Matsumura KC, Ohkawara A.
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69.) Neutrophilic dermatosis with an erythema gyratum repens-like pattern in systemic lupus erythematosus.
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Acta Derm Venereol. 2005;85(5):455-6.
Khan Durani B, Andrassy K, Hartschuh W.
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70.) Penicillin-induced anti-p200 pemphigoid: an unusual morphology.
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Acta Derm Venereol. 2006;86(5):443-6.
Wozniak K1, Kowalewski C, Hashimoto T, Ishii N, Glinska-Wielochowska M, Schwartz RA.
Author information
1Department of Dermatology, Medical University of Warsaw, PL-02008 Warsaw, Poland. kwoznia@amwaw.edu.pl
Abstract
We report here a case of a 52-year-old woman with erythema gyratum repens-like lesions appearing during anti-p200 pemphigoid, probably induced by oral penicillin. The diagnosis of anti-p200 pemphigoid was made by the presence of in vivo bound and circulating IgG anti-basement membrane zone auto-antibody reactive with the dermal side of salt-split skin and with 200 kDa protein in dermal extract on Western immunoblot. Laser scanning confocal microscopic study disclosed the localization of IgG at the lamina lucida-lamina densa border. Skin lesions responded poorly to high dose of prednisone and the combination of prednisone and dapsone. When methotrexate was added, skin lesions healed within 3 weeks. To our knowledge, erythema gyratum repens-like lesions have not been described previously in this disorder. Thus, we have expanded the clinical morphological spectrum of patients with anti-p200 pemphigoid and first described a patient whose disorder was probably drug-induced.
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REFERENCIAS BIBLIOGRAFICAS / BIBLIOGRAPHICAL REFERENCES
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40.) [Erythema gyratum repens or Gammel paraneoplastic syndrome. A case with
epidermoid carcinoma developed on a megaesophagus].
41.) Erythema gyratum repens--an immunologically mediated dermatosis?
42.) Erythema gyratum repens with metastatic adenocarcinoma.
43.) [Erythema gyratum repens (Gammel's syndrome)]
44.) Figurate and bullous eruption in association with breast carcinoma.
45.) [Erythema gyratum repens associated with bronchial carcinoma]
46.) Erythema gyratum repens. Reports of two further cases associated with
carcinoma.
47.) Carcinoma of the breast, pemphigus vulgaris and gyrate erythema.
48.) [Premycotic erythema simulating erythema gyratum repens].
49.) [An unusual paraneoplastic syndrome: erythema "gyratum repens" or Gammel's syndrome].
50.) [An unusual paraneoplastic syndrome: erythema gyratum repens. Its relation with bronchial cancer].
51.) Cutaneous manifestations of lung cancer.
52.) Cutaneous manifestations of breast cancer.
53.) Erythema gyratum repens.
54.) Erythema gyratum repens unassociated with underlying malignancy.
55.) Erythema gyratum repens unassociated with internal malignancy.
56.) Erythema gyratum repens associated with cryptogenic organizing pneumonia.
57.) Erythema gyratum repens preceding the onset of rheumatoid arthritis.
58.) Erythema gyratum repens associated with hypereosinophilic syndrome.
59.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
60.) Erythema gyratum repens is not an obligate paraneoplastic disease: a systematic review of the literature and personal experience.
61.) Novel presentation of lepromatous leprosy in an erythema gyratum repens-like pattern.
62.) Leucocytoclastic vasculitis presenting as an erythema gyratum repens-like eruption.
63.) Urticarial vasculitis presenting as erythema gyratum repens-like eruption.
64.) Erythema gyratum repens-like eruption occuring in resolving psoriasis during methotrexate therapy.
65.) Erythema gyratum repens-like eruption in a patient with epidermolysis bullosa acquisita
associated with ulcerative colitis.
66.) Erythema gyratum repens-like eruption in mycosis fungoides: is dermatophyte superinfection
underdiagnosed in cutaneous T-cell lymphomas?
67.) Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.
68.) Erythema gyratum repens-like eruption in a patient with Sjögren syndrome.
69.) Neutrophilic dermatosis with an erythema gyratum repens-like pattern in systemic lupus erythematosus.
70.) Penicillin-induced anti-p200 pemphigoid: an unusual morphology.
=============================================================
=============================================================
1.) Erythema gyratum repens: A paraneoplastic eruption; Clinical review
=============================================================
SOURCE: J AM ACAD DERMATOL 1992;26:757-62.
Alan S. Boyd, MD, Kenneth H. Neldner, MD, and Alan Menter, MD Lubbock and
Dallas, Texas
REFERENCIAS BIBLIOGRAFICAS / BIBLIOGRAPHICAL REFERENCES
==================================================================
1.) Erythema gyratum repens: A paraneoplastic eruption; Clinical review
2.) Cutaneous manifestations of cancer.
3.) Erythema gyratum repens in association with renal cell carcinoma.
4.) Erythema gyratum repens: another case of a rare disorder but no new insight into pathogenesis.
5.) Cutaneous paraneoplastic syndromes in solid tumors.
6.) Erythema gyratum repens unassociated with underlying malignancy.
7.) Erythema gyratum repens-like eruption in a patient with Sjogren syndrome.
8.) Paraneoplastic bullous pemphigoid resembling erythema gyratum repens.
9.) Eruption resembling erythema gyratum repens in linear IgA dermatosis.
10.) Erythema gyratum repens associated with hypereosinophilic syndrome.
11.) Erythema gyratum repens. A case studied with immunofluorescence,
immunoelectron microscopy and immunohistochemistry.
12.) Erythema gyratum repens: direct immunofluorescence microscopic findings.
13.) Erythema gyratum repens without underlying disease.
14.)Reactive erythemas: erythema annulare centrifugum and erythema gyratum
repens.
15.) Subcorneal accumulation of Langerhans cells in erythema gyratum repens.
16.) Erythema gyratum repens in a healthy woman.
17.)[Gammel's non-paraneoplastic erythema gyratum repens].
18.) [Erythema gyratum repens type eruption].
19.) A mechanism of peripheral spread or localization of inflammatory
reactions--role of the localized ground substance adaptive phenomenon.
20.) Episodic erythema gyratum repens with ichthyosis and palmoplantar
hyperkeratosis without signs of internal malignancy.
21.) Erythema gyratum repens. A cutaneous marker of malignancy.
22.) Bullous pemphigoid with figurate erythema associated with carcinoma of the bronchus.
23.) Erythema figuratum versus erythema gyratum repens.
24.) Erythema gyratum repens, a stage in the resolution of pityriasis rubra
pilaris?
25.)[Erythema gyratum repens--a paraneoplastic dermatosis].
26.)Erythema gyratum repens unassociated with internal malignancy.
27.) Erythema gyratum repens.
28.) Gyrate erythema.
29.) Infantile epidermodysplastic erythema gyratum responsive to imidazoles. A new entity?
30.) Erythema gyratum repens with associated squamous cell carcinoma of the lung.
31.) [Cutaneous paraneoplastic syndromes].
32.) [Erythema gyratum repens and primary bronchial cancer. Disappearance of the dermatosis under general corticoid therapy].
33.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
34.) Erythema gyratum repens-like figurate eruption in bullous pemphigoid.
35.) [Erythema gyratum repens].
36.) [Erythema gyratum repens].
37.) Erythema gyratum repens: spontaneous resolution in a healthy man.
38.) Erythema gyratum repens with pulmonary tuberculosis.
39.) [Gammel's erythema gyratum repens and acquired ichthyosis associated with esophageal carcinoma].
40.) [Erythema gyratum repens or Gammel paraneoplastic syndrome. A case with
epidermoid carcinoma developed on a megaesophagus].
41.) Erythema gyratum repens--an immunologically mediated dermatosis?
42.) Erythema gyratum repens with metastatic adenocarcinoma.
43.) [Erythema gyratum repens (Gammel's syndrome)]
44.) Figurate and bullous eruption in association with breast carcinoma.
45.) [Erythema gyratum repens associated with bronchial carcinoma]
46.) Erythema gyratum repens. Reports of two further cases associated with
carcinoma.
47.) Carcinoma of the breast, pemphigus vulgaris and gyrate erythema.
48.) [Premycotic erythema simulating erythema gyratum repens].
49.) [An unusual paraneoplastic syndrome: erythema "gyratum repens" or Gammel's syndrome].
50.) [An unusual paraneoplastic syndrome: erythema gyratum repens. Its relation with bronchial cancer].
51.) Cutaneous manifestations of lung cancer.
52.) Cutaneous manifestations of breast cancer.
53.) Erythema gyratum repens.
54.) Erythema gyratum repens unassociated with underlying malignancy.
55.) Erythema gyratum repens unassociated with internal malignancy.
56.) Erythema gyratum repens associated with cryptogenic organizing pneumonia.
57.) Erythema gyratum repens preceding the onset of rheumatoid arthritis.
58.) Erythema gyratum repens associated with hypereosinophilic syndrome.
59.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
60.) Erythema gyratum repens is not an obligate paraneoplastic disease: a systematic review of the literature and personal experience.
61.) Novel presentation of lepromatous leprosy in an erythema gyratum repens-like pattern.
62.) Leucocytoclastic vasculitis presenting as an erythema gyratum repens-like eruption.
63.) Urticarial vasculitis presenting as erythema gyratum repens-like eruption.
64.) Erythema gyratum repens-like eruption occuring in resolving psoriasis during methotrexate therapy.
65.) Erythema gyratum repens-like eruption in a patient with epidermolysis bullosa acquisita
associated with ulcerative colitis.
66.) Erythema gyratum repens-like eruption in mycosis fungoides: is dermatophyte superinfection
underdiagnosed in cutaneous T-cell lymphomas?
67.) Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.
68.) Erythema gyratum repens-like eruption in a patient with Sjögren syndrome.
69.) Neutrophilic dermatosis with an erythema gyratum repens-like pattern in systemic lupus erythematosus.
70.) Penicillin-induced anti-p200 pemphigoid: an unusual morphology.
=============================================================
=============================================================
1.) Erythema gyratum repens: A paraneoplastic eruption; Clinical review
=============================================================
SOURCE: J AM ACAD DERMATOL 1992;26:757-62.
Alan S. Boyd, MD, Kenneth H. Neldner, MD, and Alan Menter, MD Lubbock and
Dallas, Texas
Erythema gyratum repens is a slowly expanding, mildly scaling
dermatosis
with a "wood-grain" pattern and is seen in patients with an underlying
malignancy. To date oflly 49 cases have appearcd in the literature, 41 of
which (84%) were associated with a neoplasm, most commonly of the lung.
Several patients also had pruritus, palmoplantar keratoderma, ichthyosis,
vesiculobulbus lesions, and/ or eosinophilia. Histopathologic findings are
nonspecific. The skin findings usually disappear with therapy for the
underlying malignancy. (J AM ACAD DERMATOL 1992;26:757-62.)
with a "wood-grain" pattern and is seen in patients with an underlying
malignancy. To date oflly 49 cases have appearcd in the literature, 41 of
which (84%) were associated with a neoplasm, most commonly of the lung.
Several patients also had pruritus, palmoplantar keratoderma, ichthyosis,
vesiculobulbus lesions, and/ or eosinophilia. Histopathologic findings are
nonspecific. The skin findings usually disappear with therapy for the
underlying malignancy. (J AM ACAD DERMATOL 1992;26:757-62.)
The skin may be the first organ to heraLd {he presence of a
visceral
malignancy. Paraneoplastic eruptions seen with cancer include acanthosis
nigricans, acquired ichthyosis, pancreatic fat necrosis, migratory
thrombophlebitis, Sweet's syndrome, hypertrichosis lanuginosa acquisita,
and others, but one of the most specific dermatoses associated with
underlying neoplasia is that of erythema gyratum repens (EGR). We discuss
this dermatosis and review the literature.
malignancy. Paraneoplastic eruptions seen with cancer include acanthosis
nigricans, acquired ichthyosis, pancreatic fat necrosis, migratory
thrombophlebitis, Sweet's syndrome, hypertrichosis lanuginosa acquisita,
and others, but one of the most specific dermatoses associated with
underlying neoplasia is that of erythema gyratum repens (EGR). We discuss
this dermatosis and review the literature.
HISTORY
=======
Gammel1 described the first case of EGR in 1953. His patient, a
55-year-old woman, developed a scaling, pruritic eruption on her trunk and
extremities reminiscent of "knotty cypress wood grain." The eruptions was
noted to extend about 1 cm per day. A palpable axillary lymph node revealed
metastatic adenocarcinoma of the breast. A radical mastectomy was
performed that led to fading of the eruption within 48 hours and complete
clearing by 6 weeks. Neither the eruption nor the tumor recurred. The
author believed this distinctive eruption had been caused by a carcinotoxin
to which the host was allergic. He named it "erythema gyratum repens"
(repens from the Latin meaning to crawl or creep).2
Since this initial description, at least 48 additional patients have been
reported.3-46 With a few exceptions,28, 31,35,36,40,42,46 all have been afflicted with an underlying malignancy, most commonly of the lung. Figurate erythemas have been known to occur With neoplasia,47 but EGR is the most specific and may be the most distinctive.
=======
Gammel1 described the first case of EGR in 1953. His patient, a
55-year-old woman, developed a scaling, pruritic eruption on her trunk and
extremities reminiscent of "knotty cypress wood grain." The eruptions was
noted to extend about 1 cm per day. A palpable axillary lymph node revealed
metastatic adenocarcinoma of the breast. A radical mastectomy was
performed that led to fading of the eruption within 48 hours and complete
clearing by 6 weeks. Neither the eruption nor the tumor recurred. The
author believed this distinctive eruption had been caused by a carcinotoxin
to which the host was allergic. He named it "erythema gyratum repens"
(repens from the Latin meaning to crawl or creep).2
Since this initial description, at least 48 additional patients have been
reported.3-46 With a few exceptions,28, 31,35,36,40,42,46 all have been afflicted with an underlying malignancy, most commonly of the lung. Figurate erythemas have been known to occur With neoplasia,47 but EGR is the most specific and may be the most distinctive.
CLINICAL FINDINGS
=================
=================
EGR displays concentric erythematous bands48 predominantly on the trunk
and
extremities. The hands, feet, and face are usually spared.2'49
The pattern of EGR has been described as wood-grained,17' 25, 28, 35, 43
serpiginous,25 zebralike,2' 20 cypress rings,22 gyrate,43 whorled,43 and
swirls of rope25 (Fig. 1, B). The expanding borders are usually macular
but may occasionally be palpable.20 Scale is usually present14,20 and
trails the leading edge of the eruption42. The eruption of EGR
moves rapidly across the surface of the skin, usually about 1 cm per day.14
EGR may involve the entire body.12'20'25'26'40 Saika et al.23 reported a
patient in whom solely right-sided truncal lesions developed with
underlying intrahepatic metastases from an adenocarcinoma of the colon. An
overlying solitary flank lesion in a patient with ipsilateral
hypernephroma has also been observed by one of us (A. M.).
extremities. The hands, feet, and face are usually spared.2'49
The pattern of EGR has been described as wood-grained,17' 25, 28, 35, 43
serpiginous,25 zebralike,2' 20 cypress rings,22 gyrate,43 whorled,43 and
swirls of rope25 (Fig. 1, B). The expanding borders are usually macular
but may occasionally be palpable.20 Scale is usually present14,20 and
trails the leading edge of the eruption42. The eruption of EGR
moves rapidly across the surface of the skin, usually about 1 cm per day.14
EGR may involve the entire body.12'20'25'26'40 Saika et al.23 reported a
patient in whom solely right-sided truncal lesions developed with
underlying intrahepatic metastases from an adenocarcinoma of the colon. An
overlying solitary flank lesion in a patient with ipsilateral
hypernephroma has also been observed by one of us (A. M.).
Table 1 lists the associated skin findings in these patients. Most
patients
experienced some degree of pruritus.20 Ichthyosis and palmar/plantar
hyperkeratosis were also noted in 16% (8 of 49) and 10% (5 of 49) of the
patients, respectively. Three patients also had bullous pemphigoid,23,35,44
one had pemphigus vulgaris,30 and three had unspecified vesicles and
bullae7, 13, 14 during the course of the disorder.
experienced some degree of pruritus.20 Ichthyosis and palmar/plantar
hyperkeratosis were also noted in 16% (8 of 49) and 10% (5 of 49) of the
patients, respectively. Three patients also had bullous pemphigoid,23,35,44
one had pemphigus vulgaris,30 and three had unspecified vesicles and
bullae7, 13, 14 during the course of the disorder.
An approximately 2:1 male-to-female ratio was observed. The average age
was
63 years and thus far alL patients have been white. Most patients (25) had
the onset of their eruption an average of 9 months before their malignancy
was diagnosed (range 1 to 72 months). Four patients developed EGR an
average of 9 months after their tumor was detected and in two cases16,41
the eruption and neoplasm occurred simultaneously.
63 years and thus far alL patients have been white. Most patients (25) had
the onset of their eruption an average of 9 months before their malignancy
was diagnosed (range 1 to 72 months). Four patients developed EGR an
average of 9 months after their tumor was detected and in two cases16,41
the eruption and neoplasm occurred simultaneously.
Table II outlines the underlying malignancies (if any) in these
patients.
Lung cancer was the most common (16 patients [32%]), followed distantly by
esophagus (4 patients [8%]) and breast (3 patients
[6%]). In three patients a metastatic malignancy was detected but the
primary site could not be identified.14,22,25 Lymphoreticular cancers
were rare.19,37 Six patients did not have an underlying malignancy,31,35,40,42,46 and in two other cases tuberculosis28 and the
CREST syndrome36 were believed to be the cause.
Lung cancer was the most common (16 patients [32%]), followed distantly by
esophagus (4 patients [8%]) and breast (3 patients
[6%]). In three patients a metastatic malignancy was detected but the
primary site could not be identified.14,22,25 Lymphoreticular cancers
were rare.19,37 Six patients did not have an underlying malignancy,31,35,40,42,46 and in two other cases tuberculosis28 and the
CREST syndrome36 were believed to be the cause.
Laboratory evaluations were performed in some cases. Many patients
had
peripheral eosinophilia as high as 59%.29 Eosinophilia of the bone marrow
has also been described.7,46 Decreased T-ce1126'30 and increased
B-ce1126 populations have been reported, as have normal percentages for
both.31 Stankler31 demonstrated normal T-cell function in a patient with EGR but no underlying malignancy. Decreased serum levels of C3 and increased luteinizing hormone and follicle-stimulating hormone were reported in one patient.26
peripheral eosinophilia as high as 59%.29 Eosinophilia of the bone marrow
has also been described.7,46 Decreased T-ce1126'30 and increased
B-ce1126 populations have been reported, as have normal percentages for
both.31 Stankler31 demonstrated normal T-cell function in a patient with EGR but no underlying malignancy. Decreased serum levels of C3 and increased luteinizing hormone and follicle-stimulating hormone were reported in one patient.26
=============================================================
Table 1. Skin findings in 49 patients with erythema gyratum repens
=============================================================
% of |
Affected | disordes
patients |
-------------------------------------------------------------
50 Pruritus*
16 Ichthyosis 22' 26, 29, 40,41,43,45,46
lo Palmar/plantar hyperkeratosis 6,42,45,46
8 Pityriasis rubra pilaris 20, 40
6 Psoriasiform lesions10, 39,40
6 Vesicles/bullae7' 13, 14
6 Bulbus pemphigoid 23,35'44
2 Pemphigus vulgaris 30
2 Discoid lupus erythematosus 40
Table 1. Skin findings in 49 patients with erythema gyratum repens
=============================================================
% of |
Affected | disordes
patients |
-------------------------------------------------------------
50 Pruritus*
16 Ichthyosis 22' 26, 29, 40,41,43,45,46
lo Palmar/plantar hyperkeratosis 6,42,45,46
8 Pityriasis rubra pilaris 20, 40
6 Psoriasiform lesions10, 39,40
6 Vesicles/bullae7' 13, 14
6 Bulbus pemphigoid 23,35'44
2 Pemphigus vulgaris 30
2 Discoid lupus erythematosus 40
*References 1,3-7, 10, 12, 14, 17,21,22,25,27-29,37, 38,40,41,43, 45,
46, 48.
-------------------------------------------------------------
-------------------------------------------------------------
=============================================================
Table II. Underlying malignancies associated with erythema
gyratum repens*
=============================================================
% |
Patients | TyPe
-------------------------------------------------------------
32 Lung4, 9, 10, 15-18, 21,26,37,39,41,43,44,45
12 None31,35,40,42,46
8 Esophagus27, 29,32, 33
6 Breast,1, 3, 30 unknown metastatic neoplasm 4, 22, 25
4 Cervix,5,7 pharynx,8,34 stomach11,13
2 Anus,24 bladder,20 bowel,23 Hodgkins disease,38 myeloma,19 pancreas,41, prostate,20 tongue,6 uterus 12
--------------------------------------------------------------
*One patient each also had tuberculosis28 and CREST syndrome.36
--------------------------------------------------------------
Table II. Underlying malignancies associated with erythema
gyratum repens*
=============================================================
% |
Patients | TyPe
-------------------------------------------------------------
32 Lung4, 9, 10, 15-18, 21,26,37,39,41,43,44,45
12 None31,35,40,42,46
8 Esophagus27, 29,32, 33
6 Breast,1, 3, 30 unknown metastatic neoplasm 4, 22, 25
4 Cervix,5,7 pharynx,8,34 stomach11,13
2 Anus,24 bladder,20 bowel,23 Hodgkins disease,38 myeloma,19 pancreas,41, prostate,20 tongue,6 uterus 12
--------------------------------------------------------------
*One patient each also had tuberculosis28 and CREST syndrome.36
--------------------------------------------------------------
HISTOPATHOLOGY
EGR is classified among the superficial erythemas50 and as such tends
to
demonstrate generally nonspecific histopathologic features. Mild to
moderate hyperkeratosis, parakeratosis, and spongiosis are seen.43,49,
50 Acanthosis, follicular plugging, liquefactive epidermal celLs, and
epidermopoiesis of neutrophils and eosinophils have been described.7
The dermal vessels are surrounded by a lympho-histiocytic infiltrate with
occasional eosinophils.28, 37, 40, 43, 50 Mast cells may also be seen.28
The capillary endothelium may appear swollen7 and vascular proliferation
has been described.14,28 Frank vasculitis is absent. Pigmentary
incontinence45 and papillary dermal edema49 may also be seen. Subepidermal
bullae with a sparse eosinophil infiltrate was described in a patient with
EGR and bulbus pemphigoid.35
Holt and Davies26 described a patient with bronchogenic carcinoma who had
IgG and C3 deposits at the basement membrane zone detected by direct
immunofluorescence of both lesional and uninvolved skin. Indirect
immunofluorescence and immunofluorescence of metastatic nodal deposits
were negative. Other investigators have found negative direct and indirect
immunofiuorescence in biopsy specimens of EGR.39,46 Levine et al.43
described a patient Erythema gyratum repens with no immune deposits at the basement membrane zone but IgM deposition on epidermal nuclei. Phenotyping of the infiammatory infiltrate in EGR demonstrated B celís and macrophages; no T celís were found.26
demonstrate generally nonspecific histopathologic features. Mild to
moderate hyperkeratosis, parakeratosis, and spongiosis are seen.43,49,
50 Acanthosis, follicular plugging, liquefactive epidermal celLs, and
epidermopoiesis of neutrophils and eosinophils have been described.7
The dermal vessels are surrounded by a lympho-histiocytic infiltrate with
occasional eosinophils.28, 37, 40, 43, 50 Mast cells may also be seen.28
The capillary endothelium may appear swollen7 and vascular proliferation
has been described.14,28 Frank vasculitis is absent. Pigmentary
incontinence45 and papillary dermal edema49 may also be seen. Subepidermal
bullae with a sparse eosinophil infiltrate was described in a patient with
EGR and bulbus pemphigoid.35
Holt and Davies26 described a patient with bronchogenic carcinoma who had
IgG and C3 deposits at the basement membrane zone detected by direct
immunofluorescence of both lesional and uninvolved skin. Indirect
immunofluorescence and immunofluorescence of metastatic nodal deposits
were negative. Other investigators have found negative direct and indirect
immunofiuorescence in biopsy specimens of EGR.39,46 Levine et al.43
described a patient Erythema gyratum repens with no immune deposits at the basement membrane zone but IgM deposition on epidermal nuclei. Phenotyping of the infiammatory infiltrate in EGR demonstrated B celís and macrophages; no T celís were found.26
DISCUSSION
===========
Differential diagnosis of the figurate erythemas
------------------------------------------------
Erythema annulare centrifugum (EAC) is morphologically similar to EGR and
some authors believe a close relation exists between the two disorders.7
EAC usually is manifested by arcuate, polycyclic erythematous lesions that
expand slowly48 and clear centrally; it may be pruritic.49 EAC differs from
EGR in that the former is slightly palpable and "moves" much more slowly.20
Histopathologic examination shows that EAC is a deep and superficial
erythema50,51 with a lymphohistiocytic "coat-sleeve" arrangement around
blood vessels,50 mild spongiosis, and parakeratosis.49
EAC may 2,48 or may not2,52 be related to an underlying disease. It has
been reported in association with malignancies48 but also with infections
and drug intake.2,48,53 Lesions may persist indefinitely or resolve within
a few days.
Erythema chronicum migrans (ECM) is an annular eruption precipitated by
the bite of an Ixodes tick and caused by infection with Borrelia
burgdorferi.2,48,49 The lesions begin as erythematous papules that enlarge
in a circular, expansile pattern to form a red, raised, scaleless eruption
several centimeters in width.48 This usually begins several days to weeks
after the tick bite. Serum antibodies directed against Borrelia antigens
may be found.
Erythema marginatum rheumaticum is usually associated with rheumatic fever in children and is rarely seen today.2 This eruption shows swift spread-irng, erythema, and minimal induration. However, it displays no scaling, has no symptoms, is evanescent, and demonstrates a neutrophilic infiltrate on histologic examination 49,51 Patients with glucagon-producing islet cell tu-mors of the pancreas may have necrolytic migratory erythema. Lesions usually begin on dependant parts of the body, periorally and perigenitally. Arcuate and circinate red plaques with erosions, vesicles, necrosis, and desquamation are present.48 Additional diseases that may occasionally enter the differential diagnosis include subacute cutaneous discoid lupus erythematosus, tinea corporis (especially tinea imbricata), psoriasis, pityriasis rubra pilaris, familial annular erythema, and keratolytic winter erythema.
===========
Differential diagnosis of the figurate erythemas
------------------------------------------------
Erythema annulare centrifugum (EAC) is morphologically similar to EGR and
some authors believe a close relation exists between the two disorders.7
EAC usually is manifested by arcuate, polycyclic erythematous lesions that
expand slowly48 and clear centrally; it may be pruritic.49 EAC differs from
EGR in that the former is slightly palpable and "moves" much more slowly.20
Histopathologic examination shows that EAC is a deep and superficial
erythema50,51 with a lymphohistiocytic "coat-sleeve" arrangement around
blood vessels,50 mild spongiosis, and parakeratosis.49
EAC may 2,48 or may not2,52 be related to an underlying disease. It has
been reported in association with malignancies48 but also with infections
and drug intake.2,48,53 Lesions may persist indefinitely or resolve within
a few days.
Erythema chronicum migrans (ECM) is an annular eruption precipitated by
the bite of an Ixodes tick and caused by infection with Borrelia
burgdorferi.2,48,49 The lesions begin as erythematous papules that enlarge
in a circular, expansile pattern to form a red, raised, scaleless eruption
several centimeters in width.48 This usually begins several days to weeks
after the tick bite. Serum antibodies directed against Borrelia antigens
may be found.
Erythema marginatum rheumaticum is usually associated with rheumatic fever in children and is rarely seen today.2 This eruption shows swift spread-irng, erythema, and minimal induration. However, it displays no scaling, has no symptoms, is evanescent, and demonstrates a neutrophilic infiltrate on histologic examination 49,51 Patients with glucagon-producing islet cell tu-mors of the pancreas may have necrolytic migratory erythema. Lesions usually begin on dependant parts of the body, periorally and perigenitally. Arcuate and circinate red plaques with erosions, vesicles, necrosis, and desquamation are present.48 Additional diseases that may occasionally enter the differential diagnosis include subacute cutaneous discoid lupus erythematosus, tinea corporis (especially tinea imbricata), psoriasis, pityriasis rubra pilaris, familial annular erythema, and keratolytic winter erythema.
Etiology
========
========
The cause of EGR is unclear. Gammel1 believed that the underlying
tumor
altered organ proteins, thereby producing endogenous allergens and creating
a state of hypersensitivity to specific tumor antigens. Church10 injected
suspensions of his patient's tumor (lung), unaffected pulmonary tissue, and
skin intradermally into a recovered patient. In a similar experiment
Leavelí et al.14 performed an Ouchter-lony gel ditfusion with their
patient's serum and a homogenate of his tumor (undifferentiated
adenocarcinoma-type unknown). Both produced negative results. Holt and Davies,26 the only investigators to demonstrate positive immunofiuorescence
of the basement membrane in skin biopsy specimens of EGR, proposed three
possibilities: tumor neoantigens may invoke antibody production that
cross-react with endogenous skin antigens, the tumor products may alter
certain skin antigens rendering it susceptible to immunologic attack, and
tumor antigen-antibody complexes may form with subsequent cutaneous
deposition. Barber et al.28 agreed that immune complex deposition may be
operative but not neeessarily involve tumor antigens exclusively.
Evaluations of the cellular arm of the immune system in EGR have been
sparse. Investigators do not believe these lymphocyte subsets play a
significant etiologic role in the eruption.26 Jacobs et al.30 noted a
peripheral T-cell deficiency in their patient and postulated that a
compensatory B-cell hyperactivity existed. Peripheral blood lymphocytes in
one patient were not stimulated by phytohemagglutimn, tumor extract (lung), or involved skin extract.26
It seems clear that whatever factors are involved in the production of
this eruption emanate from the underlying tumor. These factors may be
produced from solid as well as hematopoietic tumors. Inherent in patients
who develop EGR is a predisposition to react in such a manner when
affiicted with cancer. Such a susceptibility could involve the human
lymphocyte antigen (HLA) system, tumoral antigen production, and/or ground
substance alterations. Specific HLA antigens have been reported to occur to a significantly greater extent in patients with malignancies of the cervix,54 testis,55 and thyroid,56 as well as in non-Hodgkin's lymphoma,57 Burkitt's lymphoma,58 and multiple myeloma.59 An interesting feature of the HLA antigens is their close relation to tumor antigens.60 These two groups of polypeptides are believed to be structurally similar with an association
existiing between the genes expressing both. Specific alleles among
patients with cancer may render them more susceptible to the development
of EGR. Second, the pathogenesis of EGR may involve a localized ground substance adaptive phenomenon. In this model granulocytes release connective
tissue active peptides, which, in turn, stimulate fibroblast proliferation
to produce ground substance with increased viscosity. 61 Thus inflammatory
mediators are impeded from tissue spread and "walled off." EGR might result
from a similar phenomenon involving spread of the erythematous rings
through stroma, which is unable to "wall off,' the attendant inflammation.
Clearing of the eruption results from a subsequent halt of this process
and clearance of the inflammatory mediators.61 Moore62 noted that the
morphologic features of EGR were similar to the patterns of aggregating
slime mould and the Belousez-Zhabotinskii chemical reaction, processes in
which reaction or diffusion systems are also operative.
altered organ proteins, thereby producing endogenous allergens and creating
a state of hypersensitivity to specific tumor antigens. Church10 injected
suspensions of his patient's tumor (lung), unaffected pulmonary tissue, and
skin intradermally into a recovered patient. In a similar experiment
Leavelí et al.14 performed an Ouchter-lony gel ditfusion with their
patient's serum and a homogenate of his tumor (undifferentiated
adenocarcinoma-type unknown). Both produced negative results. Holt and Davies,26 the only investigators to demonstrate positive immunofiuorescence
of the basement membrane in skin biopsy specimens of EGR, proposed three
possibilities: tumor neoantigens may invoke antibody production that
cross-react with endogenous skin antigens, the tumor products may alter
certain skin antigens rendering it susceptible to immunologic attack, and
tumor antigen-antibody complexes may form with subsequent cutaneous
deposition. Barber et al.28 agreed that immune complex deposition may be
operative but not neeessarily involve tumor antigens exclusively.
Evaluations of the cellular arm of the immune system in EGR have been
sparse. Investigators do not believe these lymphocyte subsets play a
significant etiologic role in the eruption.26 Jacobs et al.30 noted a
peripheral T-cell deficiency in their patient and postulated that a
compensatory B-cell hyperactivity existed. Peripheral blood lymphocytes in
one patient were not stimulated by phytohemagglutimn, tumor extract (lung), or involved skin extract.26
It seems clear that whatever factors are involved in the production of
this eruption emanate from the underlying tumor. These factors may be
produced from solid as well as hematopoietic tumors. Inherent in patients
who develop EGR is a predisposition to react in such a manner when
affiicted with cancer. Such a susceptibility could involve the human
lymphocyte antigen (HLA) system, tumoral antigen production, and/or ground
substance alterations. Specific HLA antigens have been reported to occur to a significantly greater extent in patients with malignancies of the cervix,54 testis,55 and thyroid,56 as well as in non-Hodgkin's lymphoma,57 Burkitt's lymphoma,58 and multiple myeloma.59 An interesting feature of the HLA antigens is their close relation to tumor antigens.60 These two groups of polypeptides are believed to be structurally similar with an association
existiing between the genes expressing both. Specific alleles among
patients with cancer may render them more susceptible to the development
of EGR. Second, the pathogenesis of EGR may involve a localized ground substance adaptive phenomenon. In this model granulocytes release connective
tissue active peptides, which, in turn, stimulate fibroblast proliferation
to produce ground substance with increased viscosity. 61 Thus inflammatory
mediators are impeded from tissue spread and "walled off." EGR might result
from a similar phenomenon involving spread of the erythematous rings
through stroma, which is unable to "wall off,' the attendant inflammation.
Clearing of the eruption results from a subsequent halt of this process
and clearance of the inflammatory mediators.61 Moore62 noted that the
morphologic features of EGR were similar to the patterns of aggregating
slime mould and the Belousez-Zhabotinskii chemical reaction, processes in
which reaction or diffusion systems are also operative.
Additional findings
--------------------
--------------------
Five patients with EGR (10%) also had palmo-plantar keratoderma. In
three,
no underlying malignancy was detected,42,46 one had lung cancer,45 and one
patient had a tongue carcinoma.6 Keratotic involvement of the palms and
soles has been described previously in association with esophageal
cancer63 and Bazex syndrome.64 Therefore it is not surprising that hyperkeratotic activity should appear in a subset of patients with a paraneoplastic eruption. These findings may be purely coincidental, but the high prevalence of palmoplantar thickening would make an association seem plausible.
Three patients had associated bullous pemphigoid,23,35,44 one had pemphigus
vulgaris,30 and three had vesiculobulbus eruptions not otherwise
specified.7,13, 14 All but one of these had an underlying malignancy,35
and no specific cancer was represented more than once. The association
between cancer and pemphigoid/pemphigus has been speculated on for many
years, however, it is currently believed that a link probably does not
exist.65,66 Because virtually all patients with EGR have had an underlying malignancy, the question arises, what of those who do not? Barber et al.28 published the first case of a patient with this eruption and pulmonary tuberculosis. Although their photograph fails to show the classic "knotty cypress" pattern, the patient's course appears consistent with EGR. Shortly
thereafter, Stankler31 described a healthy man with a 17-month history of
a gyrate erythema believed to be consistent with EGR that subsequently
resolved. Examination did not reveal a malignant process. No photographs
were provided. Ingber et al.36 and Juhlin et al.46 described patients with
the CREST syndrome and palmoplantar hyperkeratosis, respectively; however,
their photographic documentation is questionable for EGR. In 1985 Langlois
et al. 42 reported a patient with the classic eruption of EGR with a
negative evaluation and lack of malignancy at autopsy. The patient had had
an unexplained 30-pound weight loss. Risk factors for neoplasia in this
patient were not discussed. Finally, Cheesbrough and Williamson40 present
the best evidence for EGR unassociated with a malignancy. Their two
patients had a characteristic eruption, exhaustive work-ups, lengthy
follow-up (12 and 60 months), and, importantly, no signs or symptoms
referable to an underlying cancer. Therefore it seems clear that a few
patients with EGR and no underlying malignancy do exist. However, patients
who develop the typical eruption of this disorder should be assumed to have
an underlying cancer until proven otherwise.
no underlying malignancy was detected,42,46 one had lung cancer,45 and one
patient had a tongue carcinoma.6 Keratotic involvement of the palms and
soles has been described previously in association with esophageal
cancer63 and Bazex syndrome.64 Therefore it is not surprising that hyperkeratotic activity should appear in a subset of patients with a paraneoplastic eruption. These findings may be purely coincidental, but the high prevalence of palmoplantar thickening would make an association seem plausible.
Three patients had associated bullous pemphigoid,23,35,44 one had pemphigus
vulgaris,30 and three had vesiculobulbus eruptions not otherwise
specified.7,13, 14 All but one of these had an underlying malignancy,35
and no specific cancer was represented more than once. The association
between cancer and pemphigoid/pemphigus has been speculated on for many
years, however, it is currently believed that a link probably does not
exist.65,66 Because virtually all patients with EGR have had an underlying malignancy, the question arises, what of those who do not? Barber et al.28 published the first case of a patient with this eruption and pulmonary tuberculosis. Although their photograph fails to show the classic "knotty cypress" pattern, the patient's course appears consistent with EGR. Shortly
thereafter, Stankler31 described a healthy man with a 17-month history of
a gyrate erythema believed to be consistent with EGR that subsequently
resolved. Examination did not reveal a malignant process. No photographs
were provided. Ingber et al.36 and Juhlin et al.46 described patients with
the CREST syndrome and palmoplantar hyperkeratosis, respectively; however,
their photographic documentation is questionable for EGR. In 1985 Langlois
et al. 42 reported a patient with the classic eruption of EGR with a
negative evaluation and lack of malignancy at autopsy. The patient had had
an unexplained 30-pound weight loss. Risk factors for neoplasia in this
patient were not discussed. Finally, Cheesbrough and Williamson40 present
the best evidence for EGR unassociated with a malignancy. Their two
patients had a characteristic eruption, exhaustive work-ups, lengthy
follow-up (12 and 60 months), and, importantly, no signs or symptoms
referable to an underlying cancer. Therefore it seems clear that a few
patients with EGR and no underlying malignancy do exist. However, patients
who develop the typical eruption of this disorder should be assumed to have
an underlying cancer until proven otherwise.
TREATMENT
=========
=========
The most effective therapy for EGR is an exhaustive search for an
underlying malignancy with treatment of the primary cause. Resolution of the
Erythema gyratum repens eruption has been noted after surgery, chemother-apy, or radiotherapy.1, 3,4,9, 10'25'38 After treatment of the cancer, additional therapy for the
eruption includes topical20, 46 and systemic steroids,25, 37,42
radiotherapy,24 and azathioprine.24 Failure of topical steroids 22,24 and
vitamin A administration42 has been reported.
underlying malignancy with treatment of the primary cause. Resolution of the
Erythema gyratum repens eruption has been noted after surgery, chemother-apy, or radiotherapy.1, 3,4,9, 10'25'38 After treatment of the cancer, additional therapy for the
eruption includes topical20, 46 and systemic steroids,25, 37,42
radiotherapy,24 and azathioprine.24 Failure of topical steroids 22,24 and
vitamin A administration42 has been reported.
REFERENCES
==========
1. Gammel JA. Erythema gyratum repens.
AMA Arch Derm Syph 1953;66:494-505.
2. Harrison PM. The annular erythemas.
Int J Dermatol 1979;18:282-90.
3. Purdy MJ. Erythema gyratum repens.
Arch Dermatol 1 959;80:590- 1.
4. Schneeweiss J, Goid SC. Erythema gyratum repens.
Proc Roy Soc Med 1959;52:367-8.
5. Duperrat B, Guilaine J, Demay C. Erythema gvratum: en rapport avec un
carcinome cervical métastatique. Bulí Soc Franc Derm Syph 1961;68:20-1.
6. Duperrat B, Pringuet R, David V. Erythema gyratum repens.
Bulí Soc Franc Derm Syph 1961;68:578-82.
7. Van Dijk E. Erythema gvratum repens.
Dermatologica 1961;123:301-10.
8. Storck H, Schnyder UW, Schwarz K. Erythema gyratum repens bei
hypopharynxcarcinom. Dermatologica 1962;124:289-93.
9. Caldwell 1W. In discussion of Church RE. Bronchiolar carcinoma
presenfing as erythema gvratum perstans. Proc Roy Soc Med 1963;56:905.
10. Church RE. Bronchiolar carcinoma presenting as erythema gyratum
perstans. Proc Roy Soc Med 1963;56:904-5.
11. Woerdeman MJ. Erythema gyratum repens.
Dermatolog-ica 1964;128:391-2.
12. Le Coulant P, Texier L, Maleville J, et al. Erythema gyratum repens.
Buil Soc Franc Derm Syph 1966;73:235-6.
13. Pevny 1. Erythema gyratum repens.
Z Raut Geschlecbtslcr 1 966;40:26~70.
14. Leavelí UW, Winternitz WW, Black JR. Erytbema gyratum repens and
undifferentiated carcinoma. Arch Derma-tol 1967;95:69-72.
15. Miguérés J, Jover A, Layssol M, et al. Un syndrome para-néoplasique
rare: l'érythéme gyratum repens: Ses rapports avec le cancer bronchique. J
Franc Med Chir Thor 1967;212:313-24.
16. Pokorny' M, Hilla M. Erythema gvratum repens.
Cesk Dermatol 1969;44:200-3.
17. Solomon R. Erytbema gyratum repens [Letter].
Arch Dermatol 1969;lO0:639.
18. Hochleitner H, Bartsch G, Zelger J. Erythema gyratum repens bei
Bronchuscarcinom. Rautarzt 1970;21:1 16-9.
19. Thivolet J, Gallois P, Perrot R. Une dermatose paranéc> plasique
m6connue: l'érythema giratum repens. Rev Lyon Med 1970;19:789-95.
20. Thomson J, Stankler L. Erythema gyratum repens.
Br J Dermatol 1970;82:406-1 1.
21. Connor BL. Erythema gyratum repens: case presentafion.
Trans St Johns Hosp Dermatol Soc 1972;58:323-4.
22. Touraine R, Revaz J, Lepine J, et al. Syndrome paraneo-plasique
associant ichtyose généralisé et érythéme annu-laire.
Bulí Soc Fr Derm Syph 1972;79:623-6.
23. Saika NK, MacKie RM, McQueen A. A case of bulbus pemphigoid and figurate erythema in association with met-astatic spread ofcarcinoma.
Br J Dermatol 1973;88:33 1-4.
24. Lukowska 1, Silny W. Erythema gyratum repens jako schorzenie
paranowotworowe. Przegl Dermatol 1974; 61:785-9.
25. Skolnick M, Mainman BR. Erythema gyratum repens with metastatic
adenocarcinoma. Arch Dermatol 1975; 111:227-9.
26. Holt PJA, Davies MG. Erythema gyratum repens an ímmunologically
mediated dermatosis? Br J Dermatol 1 977;96:343-7.
27. Verret JL, Pierrin B, Bertrand G, et al. Erythema gyratum repens: 011
syndrome paranéoplasique de Gammel. Ann Dermatol Venereol 1 977;104:403-6.
28. Barber PV, Doyle L, Vickers DM, et al. Erythema gyratum repens with
pulmonary tuberculosis. Br J Dermatol 1978; 98:465-8.
29. Barriére H, Litoux P, Bureau B, et al. Erythema gyratum repens de
Gammel et ichtyose acquise associés a un cancer de l'oesophage. Ann
Dermatol Venereol 1978;105:3 19-21.
30. Jacobs R, Eng AM, Solomon LM. Carcinoma of the breast, pemphigus
vulgaris and gyrate erythema. mt J Dermatol 1978;17:221-4.
31. Stankler L. Erythema gyratum repens: spontaneous reso-lution in a
healthy man (Lerter]. Br J Dermatol 1978;99: 461.
32. Tenailleau JP. Erythema gyratum repens [Lerter].
Ann Dermatol Vénéreol 1978;105:765.
33. ChristensenjD. Erythemagyratumrepens [Letter] .
Ugeskr Laeger 1979;141:3532.
34. Ressa PG, Colombo R. Erythema gyratum repens.
G Ital Dermatol Venereol 1980;115:301-2.
35. Breathnach SM, Wilkinson JD, Black MM. Erythema gy-ratum repens-like
figurate eruption in bulbus pemphigoid. Clin Exp Dermatol 1982;7:401-6.
36. Ingber A, Pullmann H, Nowel C. CRSET Syndrom: assoziation mit erythema
figuratum. Z Hautkr 1983;58:1298-306.
37. Larrouy JC, Apter J, Baréty M, et al. Erythema gyratum repens et cancer bronchique primitif: disparition de la dermatose sous corticothérapie
gégérale. Ann Dermatol V~ néréol 1983;l 10:329-34.
38. Yebra SI, Garciá BB, Camacho MF. Eritema gyratum re-pens de Gammel y
enfirmedad de Hodgkin. Med Cutan Ibero Lat Am 1983;11:281-6.
39. Olsen TG, Milroy SK, Jones-Olsen 5. Erythema gyratum repens with
associated squamous celí carcinoma of the lung. Cutis 1 984;34:35 1-5.
40. Cheesbrough MJ, Williamson DM. Erythema gyratum repens, a stage in the
res~ution of pityriasis rubra pilaris? Clin Exp Dermatol 1985;l0:466-71.
41. Karalitski EM. Erythema gyratum repen~paraneoplas-ticheski dermatoz.
Vestn Dermatol Venereol 1985;8:49-51.
42. Langlois JC, Shaw JM, Odland GF. Erythema gyratum repens unassociated
with internal malignancy. J AM ACAD DERMATOL 1985;12:911-3.
43. Levine LE, Morgan NF, Fretzin D, et al. Erythema gyratum repens.
Arch Dermatol 1985;121:170-1.
44. Graham-Brown RAC. Bullous pemphigoid with figurate erythema associated
with carcinoma of the bronchus. Br J Dermatol 1987;l 17:385-8.
45. Appell ML, Ward WQ, Tyring SK. Erythema gyratum repens: a cutaneous
marker of malignancy. Cancer 1988; 62:548-50.
46. Juhlin L, Lacour LP, Larrouy JC, et al. Episodic erythema gyratum
repens witll ichthyosis and palmoplantar hyocrk-eratosis without sigus of
internal malignancy. Clin Exp Dermatol 1 989;14:223-6.
47. Summerly R. The figurate erythemas and neoplasia.
Br J Dermatol 1964;76:370-3.
48. Burgdorf WRC, Goltz RW. Figurate erythemas. In: Fita-patnck TB, Bisen
AZ, Wolff K, et al, eds. Dermatology in general medicine. New York:
McGraw-Hrn, 1987:1010-8.
49. White JW. Gyrate erythema.
Dermatol Clin 1985;3:l29-39.
50. Lever WF, Schaumburg-Lever G. Histopathology of the skin. Philadelphia: JB Lippincott, 1983:137-8.
51. White JW. Hypersensitivity and miscellaneous inflammatory disorders.
In: Moschella SL, Hurley HJ, eds. Dermatology. Philadelphia: WB Saunders,
l985:46-98.
52. White JW, Perry HO. Erythema perstans.
Br J Dermatol 1969;81:641-5l.
53. Sheliey WB. Erythema annulare centrifugum.
Arch Der-matol 1 964;90:54-8.
54. Sniecinski 1, Haley J, Morgan-Byrne J, et al.Histocom-patibility-antigen distribution in patients with cervical and endometrial carcinomas. Gynecol Onool 1981; 11:68-74.
55. DeWolf WC, Lange PH, Binarson ME, et al. HLA and testicular cancer.
Nature 1 979;277:21 6-7.
56. Panza N, Del Veechio L, Maio M, et al. Strong association between an
HLA-DR anfigen and thyroid carcinoma. Tissue Antigens 1982.20:155-8.
57. van den Tweel JG, Dugas DJ, Loon J, et al. HLA typing in non-Hodgkin's
lymphomas. Comparative study in caucasoids, Mexican-Americans and negroids. Tissue Anti-gens 1 982;20:364-7 1.
58. Jones EH, Biggar RJ, Nkrumah FK, et al. Study of the HLA system in
Burkitt's lymphoma. Hum Immunol 1980;3:207-l0.
59. Ludwig H, Mayr W. Genetic aspects of susceptibility to multiple
myeloma. Blood 1982;59:1286-91.
60. Gupta RK, Morton DL. Tumor antigeos. In: Ray PK, ed. Immunobiology of
transpíantation, cancer and pregnancy.
New York: Pergamon Press, 1983:113-47.
61. Stone OJ. A mechanism of peripheral spread or localization of
inflammatory reactions-role of the localized ground substance adaptive
phenomenon. Med Hypotheses 1989; 29:167-9.
62. Moore HJ. Does the pattern of erythema gyratum repens depend on a
reaction-dilfusion system? [Lerter] Br J Der-matol 1982;107:723.
63. Howel-Evans W, McConnell RB, Clarke DA, et al. Carci-noma of the
esophagus with keratosis palmaris et plantaris (tylosis). Q J Med
1958;27:413-29.
64. Richard M, Giroux J-M. Acrokeratosis paraneoplastic (Bazex syndrome). JAM ACAD DERMATOL 1987;16:178-83.
65. Stone SP, Schrocter AL. Bulbus pemphigoid and associ-ated malignant
neoplasms. Arch Dermatol 1 975;1 11:991-4.
66. Kaplan RP, Callen JP. Pemphigus-associated diseases and induced
pemphigus. Clin Dermatol 1983; 1:42-71.
=============================================================
==========
1. Gammel JA. Erythema gyratum repens.
AMA Arch Derm Syph 1953;66:494-505.
2. Harrison PM. The annular erythemas.
Int J Dermatol 1979;18:282-90.
3. Purdy MJ. Erythema gyratum repens.
Arch Dermatol 1 959;80:590- 1.
4. Schneeweiss J, Goid SC. Erythema gyratum repens.
Proc Roy Soc Med 1959;52:367-8.
5. Duperrat B, Guilaine J, Demay C. Erythema gvratum: en rapport avec un
carcinome cervical métastatique. Bulí Soc Franc Derm Syph 1961;68:20-1.
6. Duperrat B, Pringuet R, David V. Erythema gyratum repens.
Bulí Soc Franc Derm Syph 1961;68:578-82.
7. Van Dijk E. Erythema gvratum repens.
Dermatologica 1961;123:301-10.
8. Storck H, Schnyder UW, Schwarz K. Erythema gyratum repens bei
hypopharynxcarcinom. Dermatologica 1962;124:289-93.
9. Caldwell 1W. In discussion of Church RE. Bronchiolar carcinoma
presenfing as erythema gvratum perstans. Proc Roy Soc Med 1963;56:905.
10. Church RE. Bronchiolar carcinoma presenting as erythema gyratum
perstans. Proc Roy Soc Med 1963;56:904-5.
11. Woerdeman MJ. Erythema gyratum repens.
Dermatolog-ica 1964;128:391-2.
12. Le Coulant P, Texier L, Maleville J, et al. Erythema gyratum repens.
Buil Soc Franc Derm Syph 1966;73:235-6.
13. Pevny 1. Erythema gyratum repens.
Z Raut Geschlecbtslcr 1 966;40:26~70.
14. Leavelí UW, Winternitz WW, Black JR. Erytbema gyratum repens and
undifferentiated carcinoma. Arch Derma-tol 1967;95:69-72.
15. Miguérés J, Jover A, Layssol M, et al. Un syndrome para-néoplasique
rare: l'érythéme gyratum repens: Ses rapports avec le cancer bronchique. J
Franc Med Chir Thor 1967;212:313-24.
16. Pokorny' M, Hilla M. Erythema gvratum repens.
Cesk Dermatol 1969;44:200-3.
17. Solomon R. Erytbema gyratum repens [Letter].
Arch Dermatol 1969;lO0:639.
18. Hochleitner H, Bartsch G, Zelger J. Erythema gyratum repens bei
Bronchuscarcinom. Rautarzt 1970;21:1 16-9.
19. Thivolet J, Gallois P, Perrot R. Une dermatose paranéc> plasique
m6connue: l'érythema giratum repens. Rev Lyon Med 1970;19:789-95.
20. Thomson J, Stankler L. Erythema gyratum repens.
Br J Dermatol 1970;82:406-1 1.
21. Connor BL. Erythema gyratum repens: case presentafion.
Trans St Johns Hosp Dermatol Soc 1972;58:323-4.
22. Touraine R, Revaz J, Lepine J, et al. Syndrome paraneo-plasique
associant ichtyose généralisé et érythéme annu-laire.
Bulí Soc Fr Derm Syph 1972;79:623-6.
23. Saika NK, MacKie RM, McQueen A. A case of bulbus pemphigoid and figurate erythema in association with met-astatic spread ofcarcinoma.
Br J Dermatol 1973;88:33 1-4.
24. Lukowska 1, Silny W. Erythema gyratum repens jako schorzenie
paranowotworowe. Przegl Dermatol 1974; 61:785-9.
25. Skolnick M, Mainman BR. Erythema gyratum repens with metastatic
adenocarcinoma. Arch Dermatol 1975; 111:227-9.
26. Holt PJA, Davies MG. Erythema gyratum repens an ímmunologically
mediated dermatosis? Br J Dermatol 1 977;96:343-7.
27. Verret JL, Pierrin B, Bertrand G, et al. Erythema gyratum repens: 011
syndrome paranéoplasique de Gammel. Ann Dermatol Venereol 1 977;104:403-6.
28. Barber PV, Doyle L, Vickers DM, et al. Erythema gyratum repens with
pulmonary tuberculosis. Br J Dermatol 1978; 98:465-8.
29. Barriére H, Litoux P, Bureau B, et al. Erythema gyratum repens de
Gammel et ichtyose acquise associés a un cancer de l'oesophage. Ann
Dermatol Venereol 1978;105:3 19-21.
30. Jacobs R, Eng AM, Solomon LM. Carcinoma of the breast, pemphigus
vulgaris and gyrate erythema. mt J Dermatol 1978;17:221-4.
31. Stankler L. Erythema gyratum repens: spontaneous reso-lution in a
healthy man (Lerter]. Br J Dermatol 1978;99: 461.
32. Tenailleau JP. Erythema gyratum repens [Lerter].
Ann Dermatol Vénéreol 1978;105:765.
33. ChristensenjD. Erythemagyratumrepens [Letter] .
Ugeskr Laeger 1979;141:3532.
34. Ressa PG, Colombo R. Erythema gyratum repens.
G Ital Dermatol Venereol 1980;115:301-2.
35. Breathnach SM, Wilkinson JD, Black MM. Erythema gy-ratum repens-like
figurate eruption in bulbus pemphigoid. Clin Exp Dermatol 1982;7:401-6.
36. Ingber A, Pullmann H, Nowel C. CRSET Syndrom: assoziation mit erythema
figuratum. Z Hautkr 1983;58:1298-306.
37. Larrouy JC, Apter J, Baréty M, et al. Erythema gyratum repens et cancer bronchique primitif: disparition de la dermatose sous corticothérapie
gégérale. Ann Dermatol V~ néréol 1983;l 10:329-34.
38. Yebra SI, Garciá BB, Camacho MF. Eritema gyratum re-pens de Gammel y
enfirmedad de Hodgkin. Med Cutan Ibero Lat Am 1983;11:281-6.
39. Olsen TG, Milroy SK, Jones-Olsen 5. Erythema gyratum repens with
associated squamous celí carcinoma of the lung. Cutis 1 984;34:35 1-5.
40. Cheesbrough MJ, Williamson DM. Erythema gyratum repens, a stage in the
res~ution of pityriasis rubra pilaris? Clin Exp Dermatol 1985;l0:466-71.
41. Karalitski EM. Erythema gyratum repen~paraneoplas-ticheski dermatoz.
Vestn Dermatol Venereol 1985;8:49-51.
42. Langlois JC, Shaw JM, Odland GF. Erythema gyratum repens unassociated
with internal malignancy. J AM ACAD DERMATOL 1985;12:911-3.
43. Levine LE, Morgan NF, Fretzin D, et al. Erythema gyratum repens.
Arch Dermatol 1985;121:170-1.
44. Graham-Brown RAC. Bullous pemphigoid with figurate erythema associated
with carcinoma of the bronchus. Br J Dermatol 1987;l 17:385-8.
45. Appell ML, Ward WQ, Tyring SK. Erythema gyratum repens: a cutaneous
marker of malignancy. Cancer 1988; 62:548-50.
46. Juhlin L, Lacour LP, Larrouy JC, et al. Episodic erythema gyratum
repens witll ichthyosis and palmoplantar hyocrk-eratosis without sigus of
internal malignancy. Clin Exp Dermatol 1 989;14:223-6.
47. Summerly R. The figurate erythemas and neoplasia.
Br J Dermatol 1964;76:370-3.
48. Burgdorf WRC, Goltz RW. Figurate erythemas. In: Fita-patnck TB, Bisen
AZ, Wolff K, et al, eds. Dermatology in general medicine. New York:
McGraw-Hrn, 1987:1010-8.
49. White JW. Gyrate erythema.
Dermatol Clin 1985;3:l29-39.
50. Lever WF, Schaumburg-Lever G. Histopathology of the skin. Philadelphia: JB Lippincott, 1983:137-8.
51. White JW. Hypersensitivity and miscellaneous inflammatory disorders.
In: Moschella SL, Hurley HJ, eds. Dermatology. Philadelphia: WB Saunders,
l985:46-98.
52. White JW, Perry HO. Erythema perstans.
Br J Dermatol 1969;81:641-5l.
53. Sheliey WB. Erythema annulare centrifugum.
Arch Der-matol 1 964;90:54-8.
54. Sniecinski 1, Haley J, Morgan-Byrne J, et al.Histocom-patibility-antigen distribution in patients with cervical and endometrial carcinomas. Gynecol Onool 1981; 11:68-74.
55. DeWolf WC, Lange PH, Binarson ME, et al. HLA and testicular cancer.
Nature 1 979;277:21 6-7.
56. Panza N, Del Veechio L, Maio M, et al. Strong association between an
HLA-DR anfigen and thyroid carcinoma. Tissue Antigens 1982.20:155-8.
57. van den Tweel JG, Dugas DJ, Loon J, et al. HLA typing in non-Hodgkin's
lymphomas. Comparative study in caucasoids, Mexican-Americans and negroids. Tissue Anti-gens 1 982;20:364-7 1.
58. Jones EH, Biggar RJ, Nkrumah FK, et al. Study of the HLA system in
Burkitt's lymphoma. Hum Immunol 1980;3:207-l0.
59. Ludwig H, Mayr W. Genetic aspects of susceptibility to multiple
myeloma. Blood 1982;59:1286-91.
60. Gupta RK, Morton DL. Tumor antigeos. In: Ray PK, ed. Immunobiology of
transpíantation, cancer and pregnancy.
New York: Pergamon Press, 1983:113-47.
61. Stone OJ. A mechanism of peripheral spread or localization of
inflammatory reactions-role of the localized ground substance adaptive
phenomenon. Med Hypotheses 1989; 29:167-9.
62. Moore HJ. Does the pattern of erythema gyratum repens depend on a
reaction-dilfusion system? [Lerter] Br J Der-matol 1982;107:723.
63. Howel-Evans W, McConnell RB, Clarke DA, et al. Carci-noma of the
esophagus with keratosis palmaris et plantaris (tylosis). Q J Med
1958;27:413-29.
64. Richard M, Giroux J-M. Acrokeratosis paraneoplastic (Bazex syndrome). JAM ACAD DERMATOL 1987;16:178-83.
65. Stone SP, Schrocter AL. Bulbus pemphigoid and associ-ated malignant
neoplasms. Arch Dermatol 1 975;1 11:991-4.
66. Kaplan RP, Callen JP. Pemphigus-associated diseases and induced
pemphigus. Clin Dermatol 1983; 1:42-71.
=============================================================
=============================================================
2.) Cutaneous manifestations of cancer.
=============================================================
Curr Opin Oncol 1999 Mar;11(2):139-44 Related Articles, Books
2.) Cutaneous manifestations of cancer.
=============================================================
Curr Opin Oncol 1999 Mar;11(2):139-44 Related Articles, Books
Sabir S, James WD, Schuchter LM
Hematology-Oncology Division, Hospital of the University of
Pennsylvania,
Philadelphia 19104, USA.
Philadelphia 19104, USA.
The appearance of skin lesions in patients with occult or obvious
malignancy may be of extreme value in the detection and management of
cancer because the skin is readily accessible to examination and biopsy.
Examination of the skin of our patients can provide important insights into
underlying malignant processes or possible complications from cancer
treatment. The range of cutaneous abnormalities is wide, and include
cutaneous paraneoplastic syndromes such as xanthomas, acanthosis nigricans,
carcinoid syndrome, unusual erythematous eruptions such as erythema gyratum
repens, and a number of genetic syndromes associated with malignancies and
inherited dermatoses.
malignancy may be of extreme value in the detection and management of
cancer because the skin is readily accessible to examination and biopsy.
Examination of the skin of our patients can provide important insights into
underlying malignant processes or possible complications from cancer
treatment. The range of cutaneous abnormalities is wide, and include
cutaneous paraneoplastic syndromes such as xanthomas, acanthosis nigricans,
carcinoid syndrome, unusual erythematous eruptions such as erythema gyratum
repens, and a number of genetic syndromes associated with malignancies and
inherited dermatoses.
=============================================================
3.) Erythema gyratum repens in association with renal cell carcinoma.
=============================================================
J Urol 1998 Jun;159(6):2077 Related Articles, Books, LinkOut
3.) Erythema gyratum repens in association with renal cell carcinoma.
=============================================================
J Urol 1998 Jun;159(6):2077 Related Articles, Books, LinkOut
Kwatra A, McDonald RE, Corriere JN Jr
Department of Surgery, University of Texas Medical School, Houston,
USA.
=============================================================
=============================================================
=============================================================
4.) Erythema gyratum repens: another case of a rare disorder but no new insight into pathogenesis.
=============================================================
Dermatology 1996;193(4):336-7 Related Articles, Books
4.) Erythema gyratum repens: another case of a rare disorder but no new insight into pathogenesis.
=============================================================
Dermatology 1996;193(4):336-7 Related Articles, Books
Rojo Sanchez S, Suarez Fernandez R, de Eusebio Murillo E, Lopez Bran
E,
Sanchez de Paz F, Robledo Aguilar A
Sanchez de Paz F, Robledo Aguilar A
Department of Dermatology, Hospital Universitario San Carlos, Madrid,
Spain.
Erythema gyratum repens (EGR) is an uncommon but distinctive
dermatosis
characterized by marble-like swirls of erythema and a thin covering scale
over the trunk, axillae and groins which has been associated with
malignancy. Bronchial carcinoma has been the most frequent neoplasm
associated. A case of EGR in a 50-year-old man with carcinoma of the lung
is reported. The onset of dermatosis preceded the discovery of the neoplasm
by 9 months. Oral corticosteroids induced the disappearance of the skin
lesions. No recurrence was observed after discontinuation of the treatment.
The patient died 1 year after the onset of dermatosis.
characterized by marble-like swirls of erythema and a thin covering scale
over the trunk, axillae and groins which has been associated with
malignancy. Bronchial carcinoma has been the most frequent neoplasm
associated. A case of EGR in a 50-year-old man with carcinoma of the lung
is reported. The onset of dermatosis preceded the discovery of the neoplasm
by 9 months. Oral corticosteroids induced the disappearance of the skin
lesions. No recurrence was observed after discontinuation of the treatment.
The patient died 1 year after the onset of dermatosis.
=============================================================
5.) Cutaneous paraneoplastic syndromes in solid tumors.
=============================================================
Am J Med 1995 Dec;99(6):662-71 Related Articles, Books
5.) Cutaneous paraneoplastic syndromes in solid tumors.
=============================================================
Am J Med 1995 Dec;99(6):662-71 Related Articles, Books
Kurzrock R, Cohen PR
Department of Clinical Investigation, University of Texas M.D.
Anderson
Cancer Center, Houston 77030, USA.
Cancer Center, Houston 77030, USA.
OBJECTIVE: To provide an overview of the clinical manifestations,
pathophysiology, and oncologic implications of the cutaneous paraneoplastic
syndromes that occur predominantly in patients with solid tumors. METHODS:
A review was performed of the literature identified by a comprehensive
MEDLINE search. RESULTS: Diverse cutaneous paraneoplastic syndromes may be
associated with underlying tumors. They include musculoskeletal disorders
(clubbing, hypertrophic osteoarthropathy, dermatomyositis, and multicentric
reticulohistiocytosis), reactive erythemas (erythema gyratum repens and
necrolytic migratory erythema), vascular dermatoses (Trousseau's syndrome),
papulosquamous disorders (acanthosis nigricans, tripe palms, palmar
hyperkeratosis, acquired ichthyosis, pityriasis rotunda, Bazex's syndrome,
florid cutaneous papillomatosis, the sign of Leser-Trelat, and extramammary
Paget's disease), and disorders of hair growth (hypertrichosis lanuginosa
acquisita). The clinical manifestations of these dermatoses may precede,
coincide with, or follow the diagnosis of cancer. The presence of a
cutaneous paraneoplastic syndrome is often associated with a poor
prognosis. CONCLUSIONS: Cutaneous paraneoplastic syndromes are specific
constellations of mucous membrane and/or skin abnormalities that are caused
by an underlying tumor. Since they may be the presenting sign of an occult
cancer, cognizance of their features and clinical implications are of
considerable importance. Individuals with these syndromes should have a
thorough workup for an associated malignancy.
pathophysiology, and oncologic implications of the cutaneous paraneoplastic
syndromes that occur predominantly in patients with solid tumors. METHODS:
A review was performed of the literature identified by a comprehensive
MEDLINE search. RESULTS: Diverse cutaneous paraneoplastic syndromes may be
associated with underlying tumors. They include musculoskeletal disorders
(clubbing, hypertrophic osteoarthropathy, dermatomyositis, and multicentric
reticulohistiocytosis), reactive erythemas (erythema gyratum repens and
necrolytic migratory erythema), vascular dermatoses (Trousseau's syndrome),
papulosquamous disorders (acanthosis nigricans, tripe palms, palmar
hyperkeratosis, acquired ichthyosis, pityriasis rotunda, Bazex's syndrome,
florid cutaneous papillomatosis, the sign of Leser-Trelat, and extramammary
Paget's disease), and disorders of hair growth (hypertrichosis lanuginosa
acquisita). The clinical manifestations of these dermatoses may precede,
coincide with, or follow the diagnosis of cancer. The presence of a
cutaneous paraneoplastic syndrome is often associated with a poor
prognosis. CONCLUSIONS: Cutaneous paraneoplastic syndromes are specific
constellations of mucous membrane and/or skin abnormalities that are caused
by an underlying tumor. Since they may be the presenting sign of an occult
cancer, cognizance of their features and clinical implications are of
considerable importance. Individuals with these syndromes should have a
thorough workup for an associated malignancy.
=============================================================
6.) Erythema gyratum repens unassociated with underlying malignancy.
=============================================================
J Dermatol 1995 Aug;22(8):587-9 Related Articles, Books
6.) Erythema gyratum repens unassociated with underlying malignancy.
=============================================================
J Dermatol 1995 Aug;22(8):587-9 Related Articles, Books
Kawakami T, Saito R
Second Department of Dermatology, Toho University School of
Medicine,
Tokyo, Japan.
Tokyo, Japan.
A case of erythema gyratum repens occurring in a 62-year-old woman
is
presented together with a review of the literature. Evaluation and
follow-up for the development of malignancy over a 32-month period failed
to reveal any evidence of malignancy. Formerly, all cases of erythema
gyratum repens were evaluated in terms of an association with an underlying
malignant disorder. To date, only sixty cases have been reported in the
literature; 14 (23%) were not found to be associated with any neoplasm.
Therefore, this term is now also used for cases unassociated with
malignancy. Erythema gyratum repens is a cutaneous eruption with a
characteristic diagnostic morphology resembling a wood grain pattern.
presented together with a review of the literature. Evaluation and
follow-up for the development of malignancy over a 32-month period failed
to reveal any evidence of malignancy. Formerly, all cases of erythema
gyratum repens were evaluated in terms of an association with an underlying
malignant disorder. To date, only sixty cases have been reported in the
literature; 14 (23%) were not found to be associated with any neoplasm.
Therefore, this term is now also used for cases unassociated with
malignancy. Erythema gyratum repens is a cutaneous eruption with a
characteristic diagnostic morphology resembling a wood grain pattern.
=============================================================
7.) Erythema gyratum repens-like eruption in a patient with Sjogren syndrome.
=============================================================
Acta Derm Venereol 1995 Jul;75(4):327 Related Articles, Books
7.) Erythema gyratum repens-like eruption in a patient with Sjogren syndrome.
=============================================================
Acta Derm Venereol 1995 Jul;75(4):327 Related Articles, Books
Matsumura T, Kumakiri M, Sato-Matsumura KC, Ohkawara A
Publication Types:
Letter
=============================================================
=============================================================
8.) Paraneoplastic bullous pemphigoid resembling erythema gyratum repens.
Br J Dermatol 1999 Mar;140(3):550-2 Related Articles, Books, LinkOut
=============================================================
Hauschild A, Swensson O, Christophers E
Letter
=============================================================
=============================================================
8.) Paraneoplastic bullous pemphigoid resembling erythema gyratum repens.
Br J Dermatol 1999 Mar;140(3):550-2 Related Articles, Books, LinkOut
=============================================================
Hauschild A, Swensson O, Christophers E
Publication Types:
Letter
=============================================================
=============================================================
9.) Eruption resembling erythema gyratum repens in linear IgA dermatosis.
=============================================================
Dermatology 1995;190(3):235-7 Related Articles, Books
Letter
=============================================================
=============================================================
9.) Eruption resembling erythema gyratum repens in linear IgA dermatosis.
=============================================================
Dermatology 1995;190(3):235-7 Related Articles, Books
Caputo R, Bencini PL, Vigo GP, Berti E, Veraldi S
Istituto di Scienze Dermatologiche, Universita di Milano,
Ospedale
Policlinico IRCCS, Italia.
Policlinico IRCCS, Italia.
We report a case of linear IgA dermatosis associated with
eruptions
resembling erythema gyratum repens in a 62-year-old man. The patient
revealed no clinical and laboratory evidence of an underlying malignancy.
The presence of eruptions similar to erythema gyratum repens during the
course of bullous dermatoses has been described in only eight reports.
resembling erythema gyratum repens in a 62-year-old man. The patient
revealed no clinical and laboratory evidence of an underlying malignancy.
The presence of eruptions similar to erythema gyratum repens during the
course of bullous dermatoses has been described in only eight reports.
=============================================================
10.) Erythema gyratum repens associated with hypereosinophilic syndrome.
=============================================================
J Dermatol 1994 Aug;21(8):612-4 Related Articles, Books
10.) Erythema gyratum repens associated with hypereosinophilic syndrome.
=============================================================
J Dermatol 1994 Aug;21(8):612-4 Related Articles, Books
Morita A, Sakakibara N, Tsuji T
Department of Dermatology, Nagoya City University Medical School,
Japan.
We report a case of typical erythema gyratum repens lesions observed as
a
manifestation of idiopathic hypereosinophilic syndrome in a 63-year-old
man. While erythema gyratum repens is usually associated with malignancy,
an intensive search over a 30-month period failed to reveal any evidence of
neoplasm. With administration of dapsone, the typical gyrate lesions
disappeared as the subject's hypereosinophilia improved.
manifestation of idiopathic hypereosinophilic syndrome in a 63-year-old
man. While erythema gyratum repens is usually associated with malignancy,
an intensive search over a 30-month period failed to reveal any evidence of
neoplasm. With administration of dapsone, the typical gyrate lesions
disappeared as the subject's hypereosinophilia improved.
=============================================================
11.) Erythema gyratum repens. A case studied with immunofluorescence,
immunoelectron microscopy and immunohistochemistry.
=============================================================
Br J Dermatol 1994 Jul;131(1):102-7 Related Articles, Books
11.) Erythema gyratum repens. A case studied with immunofluorescence,
immunoelectron microscopy and immunohistochemistry.
=============================================================
Br J Dermatol 1994 Jul;131(1):102-7 Related Articles, Books
Caux F, Lebbe C, Thomine E, Benyahia B, Flageul B, Joly P, Rybojad M,
Morel P
Service de Dermatologie, Hopital Saint-Louis, Paris,
France.
We report a patient with erythema gyratum repens (EGR), in whom a
bronchial
carcinoma was found. Direct immunofluorescence revealed granular deposits
of immunoglobulins at the basement membrane zone (BMZ) in the skin, and in
the lung tumour. Direct immunoelectron microscopy showed that the immune
deposits were localized just beneath the lamina densa. Indirect
immunofluorescence revealed circulating anti-BMZ antibodies.
Immunohistochemical staining, using anti-transforming growth factor-beta,
anti-epidermal growth factor receptor, anti-vimentin and anti-alpha-actin,
was found to be more intense in the lesional skin and the lung tumour than
in normal tissues. Possible mechanisms in the pathogenesis of EGR are
discussed.
carcinoma was found. Direct immunofluorescence revealed granular deposits
of immunoglobulins at the basement membrane zone (BMZ) in the skin, and in
the lung tumour. Direct immunoelectron microscopy showed that the immune
deposits were localized just beneath the lamina densa. Indirect
immunofluorescence revealed circulating anti-BMZ antibodies.
Immunohistochemical staining, using anti-transforming growth factor-beta,
anti-epidermal growth factor receptor, anti-vimentin and anti-alpha-actin,
was found to be more intense in the lesional skin and the lung tumour than
in normal tissues. Possible mechanisms in the pathogenesis of EGR are
discussed.
=============================================================
12.) Erythema gyratum repens: direct immunofluorescence microscopic findings.
=============================================================
J Am Acad Dermatol 1993 Sep;29(3):493-4 Related Articles, Books,
LinkOut
12.) Erythema gyratum repens: direct immunofluorescence microscopic findings.
=============================================================
J Am Acad Dermatol 1993 Sep;29(3):493-4 Related Articles, Books,
LinkOut
Albers SE, Fenske NA, Glass LF
Department of Internal Medicine, University of South Florida, College
of
Medicine.
=============================================================
=============================================================
13.) Erythema gyratum repens without underlying disease.
=============================================================
J Am Acad Dermatol 1993 Jan;28(1):132 Related Articles, Books, LinkOut
Medicine.
=============================================================
=============================================================
13.) Erythema gyratum repens without underlying disease.
=============================================================
J Am Acad Dermatol 1993 Jan;28(1):132 Related Articles, Books, LinkOut
Boyd AS, Neldner KH
Publication Types:
Comment
Letter
=============================================================
=============================================================
14.)Reactive erythemas: erythema annulare centrifugum and erythema gyratum
repens.
=============================================================
Clin Dermatol 1993 Jan-Mar;11(1):135-9 Related Articles, Books
Tyring SK
Publication Types:
Comment
Letter
=============================================================
=============================================================
14.)Reactive erythemas: erythema annulare centrifugum and erythema gyratum
repens.
=============================================================
Clin Dermatol 1993 Jan-Mar;11(1):135-9 Related Articles, Books
Tyring SK
Department of Dermatology, University of Texas Medical Branch,
Galveston.
Publication Types:
Review
Review, tutorial
=============================================================
=============================================================
15.) Subcorneal accumulation of Langerhans cells in erythema gyratum repens.
=============================================================
Br J Dermatol 1992 Feb;126(2):189-92 Related Articles, Books
Review
Review, tutorial
=============================================================
=============================================================
15.) Subcorneal accumulation of Langerhans cells in erythema gyratum repens.
=============================================================
Br J Dermatol 1992 Feb;126(2):189-92 Related Articles, Books
Wakeel RA, Ormerod AD, Sewell HF, White MI
Department of Dermatology, Aberdeen Royal Infirmary, U.K.
Erythema gyratum repens (EGR) is a cutaneous manifestation of
malignant
disease. We report an unusual accumulation of activated epidermal
Langerhans cells in the upper layer of the epidermis and propose that these
cells play an important immunopathological role.
disease. We report an unusual accumulation of activated epidermal
Langerhans cells in the upper layer of the epidermis and propose that these
cells play an important immunopathological role.
=============================================================
16.) Erythema gyratum repens in a healthy woman.
=============================================================
J Am Acad Dermatol 1992 Jan;26(1):121-2 Related Articles, Books
16.) Erythema gyratum repens in a healthy woman.
=============================================================
J Am Acad Dermatol 1992 Jan;26(1):121-2 Related Articles, Books
Garrett SJ, Roenigk HH Jr
Department of Dermatology, Northwestern University Medical School,
Chicago,
IL 60611.
IL 60611.
Comments:
Comment in: J Am Acad Dermatol 1993 Jan;28(1):132
=============================================================
Comment in: J Am Acad Dermatol 1993 Jan;28(1):132
=============================================================
=============================================================
17.)[Gammel's non-paraneoplastic erythema gyratum repens].
=============================================================
Ann Dermatol Venereol 1991;118(6-7):469 Related Articles, Books
17.)[Gammel's non-paraneoplastic erythema gyratum repens].
=============================================================
Ann Dermatol Venereol 1991;118(6-7):469 Related Articles, Books
[Article in French]
Bazex J, Marguery MC
Service de Dermatologie, Allergologie et Venereologie, Hopital
Purpan,
Toulouse.
Toulouse.
Publication Types:
Review
Review of reported cases
=============================================================
=============================================================
18.) [Erythema gyratum repens type eruption].
=============================================================
Ann Dermatol Venereol 1991;118(11):897-9 Related Articles, Books
Review
Review of reported cases
=============================================================
=============================================================
18.) [Erythema gyratum repens type eruption].
=============================================================
Ann Dermatol Venereol 1991;118(11):897-9 Related Articles, Books
Goettmann S, Lazareth I, Crickx B, Lemaire V, Belaich S
Service de Dermatologie, Hopital Bichat, Paris.
=============================================================
=============================================================
19.) A mechanism of peripheral spread or localization of inflammatory
reactions--role of the localized ground substance adaptive phenomenon.
=============================================================
Med Hypotheses 1989 Jul;29(3):167-9 Related Articles, Books
=============================================================
=============================================================
19.) A mechanism of peripheral spread or localization of inflammatory
reactions--role of the localized ground substance adaptive phenomenon.
=============================================================
Med Hypotheses 1989 Jul;29(3):167-9 Related Articles, Books
Stone OJ
It is known that connective tissue-active peptides (CTAP) are released
at
sites of inflammation. Some of this material diffuses to immediately
adjacent tissue and increases ground substance viscosity and fibroblast
proliferation. This contributes to host protection against spread of
infections and tumors. In a person with normal inflammatory reactivity, it
should prevent spread of mediators and products of local inflammation.
However, the host with an increased reactivity in sites of increased ground
substance viscosity or who is highly reactive to dilution of tissue fluid
would respond with more inflammation. A non-infectious, non-malignant
process in a host with a highly reactive inflammatory or immune response
could end up with peripheral spread. This could occur in any tissue but it
occurs with great vigor in the skin. It could present as a peripheral
extension of a local disease process, such as psoriasis, or the migration
of cyclic lesions with clearing of the central area. There are over a dozen
variants of peripherally spreading, ringed lesions described in the
dermatologic literature. This includes erythema marginatum of rheumatic
fever, erythema gyratum repens associated with cancer, and erythema
annulare centrificum associated with allergic reactions to fungi. Many of
the ringed dermatologic lesions have an immunologic component. They tend to
be associated with inflammatory immune reactions at distant sites.
Dermatologists have been gathering information on the ringed phenomenon at
least since Hebra in 1854. The acute localized ground substance adaptive
phenomenon is a broadly beneficial biologic response.
sites of inflammation. Some of this material diffuses to immediately
adjacent tissue and increases ground substance viscosity and fibroblast
proliferation. This contributes to host protection against spread of
infections and tumors. In a person with normal inflammatory reactivity, it
should prevent spread of mediators and products of local inflammation.
However, the host with an increased reactivity in sites of increased ground
substance viscosity or who is highly reactive to dilution of tissue fluid
would respond with more inflammation. A non-infectious, non-malignant
process in a host with a highly reactive inflammatory or immune response
could end up with peripheral spread. This could occur in any tissue but it
occurs with great vigor in the skin. It could present as a peripheral
extension of a local disease process, such as psoriasis, or the migration
of cyclic lesions with clearing of the central area. There are over a dozen
variants of peripherally spreading, ringed lesions described in the
dermatologic literature. This includes erythema marginatum of rheumatic
fever, erythema gyratum repens associated with cancer, and erythema
annulare centrificum associated with allergic reactions to fungi. Many of
the ringed dermatologic lesions have an immunologic component. They tend to
be associated with inflammatory immune reactions at distant sites.
Dermatologists have been gathering information on the ringed phenomenon at
least since Hebra in 1854. The acute localized ground substance adaptive
phenomenon is a broadly beneficial biologic response.
=============================================================
20.) Episodic erythema gyratum repens with ichthyosis and palmoplantar
hyperkeratosis without signs of internal malignancy.
=============================================================
Clin Exp Dermatol 1989 May;14(3):223-6 Related Articles, Books
20.) Episodic erythema gyratum repens with ichthyosis and palmoplantar
hyperkeratosis without signs of internal malignancy.
=============================================================
Clin Exp Dermatol 1989 May;14(3):223-6 Related Articles, Books
Juhlin L, Lacour JP, Larrouy JC, Baze PE, Ortonne JP
Two patients with typical lesions of erythema gyratum repens,
peripheral
ichthyosis, palmoplantar hyperkeratosis and nail changes are described. A
non-specific erythrodermic eruption of several weeks' duration had preceded
the typical lesions. No signs of internal malignancy were found and the
typical gyrate lesions disappeared within some weeks with full restitution
of all skin lesions within 6-8 months.
ichthyosis, palmoplantar hyperkeratosis and nail changes are described. A
non-specific erythrodermic eruption of several weeks' duration had preceded
the typical lesions. No signs of internal malignancy were found and the
typical gyrate lesions disappeared within some weeks with full restitution
of all skin lesions within 6-8 months.
=============================================================
21.) Erythema gyratum repens. A cutaneous marker of malignancy.
=============================================================
Cancer 1988 Aug 1;62(3):548-50 Related Articles, Books
Appell ML, Ward WQ, Tyring SK
21.) Erythema gyratum repens. A cutaneous marker of malignancy.
=============================================================
Cancer 1988 Aug 1;62(3):548-50 Related Articles, Books
Appell ML, Ward WQ, Tyring SK
Department of Dermatology, University of Alabama,
Birmingham.
A patient with erythema gyratum repens in whom a bronchogenic carcinoma
was
found is described. Erythema gyratum repens is a cutaneous eruption with a
unique morphology resembling a wood grain pattern. Its presence is almost
always associated with serious systemic pathology, usually neoplastic, and
thus should be considered a cutaneous marker of internal malignancy.
found is described. Erythema gyratum repens is a cutaneous eruption with a
unique morphology resembling a wood grain pattern. Its presence is almost
always associated with serious systemic pathology, usually neoplastic, and
thus should be considered a cutaneous marker of internal malignancy.
=============================================================
22.) Bullous pemphigoid with figurate erythema associated with carcinoma of the bronchus.
=============================================================
Br J Dermatol 1987 Sep;117(3):385-8 Related Articles, Books
22.) Bullous pemphigoid with figurate erythema associated with carcinoma of the bronchus.
=============================================================
Br J Dermatol 1987 Sep;117(3):385-8 Related Articles, Books
Graham-Brown RA
Department of Dermatology, Leicester Royal Infirmary, Infirmary Square, U.K.
Department of Dermatology, Leicester Royal Infirmary, Infirmary Square, U.K.
A patient with bullous pemphigoid (BP), a figurate erythema
resembling
erythema gyratum repens and a bronchial carcinoma is reported. It is
suggested that this is a genuine association and that when a figurate
erythema occurs with BP, an underlying carcinoma should be excluded.
erythema gyratum repens and a bronchial carcinoma is reported. It is
suggested that this is a genuine association and that when a figurate
erythema occurs with BP, an underlying carcinoma should be excluded.
=============================================================
23.) Erythema figuratum versus erythema gyratum repens.
=============================================================
J Am Acad Dermatol 1986 Jul;15(1):111-2 Related Articles, Books
23.) Erythema figuratum versus erythema gyratum repens.
=============================================================
J Am Acad Dermatol 1986 Jul;15(1):111-2 Related Articles, Books
Ingber A, Sandbank M
Publication Types:
Letter
=============================================================
=============================================================
24.) Erythema gyratum repens, a stage in the resolution of pityriasis rubra
pilaris?
=============================================================
Clin Exp Dermatol 1985 Sep;10(5):466-71 Related Articles, Books
Letter
=============================================================
=============================================================
24.) Erythema gyratum repens, a stage in the resolution of pityriasis rubra
pilaris?
=============================================================
Clin Exp Dermatol 1985 Sep;10(5):466-71 Related Articles, Books
Cheesbrough MJ, Williamson DM
=============================================================
=============================================================
25.)[Erythema gyratum repens--a paraneoplastic dermatosis].
=============================================================
Vestn Dermatol Venerol 1985 Aug;(8):49-51 Related Articles, Books
=============================================================
=============================================================
25.)[Erythema gyratum repens--a paraneoplastic dermatosis].
=============================================================
Vestn Dermatol Venerol 1985 Aug;(8):49-51 Related Articles, Books
[Article in Russian]
Karalitskii EM
=============================================================
=============================================================
26.)Erythema gyratum repens unassociated with internal malignancy.
=============================================================
J Am Acad Dermatol 1985 May;12(5 Pt 2):911-3 Related Articles, Books
=============================================================
=============================================================
26.)Erythema gyratum repens unassociated with internal malignancy.
=============================================================
J Am Acad Dermatol 1985 May;12(5 Pt 2):911-3 Related Articles, Books
Langlois JC, Shaw JM, Odland GF
A case report of erythema gyratum repens occurring in a 68-year-old man
is
presented. Evaluation and follow-up for development of malignancy over a
39-month period failed to reveal evidence of malignancy. The patient died
of an unrelated cause. Autopsy did not demonstrate any evidence of malignancy.
presented. Evaluation and follow-up for development of malignancy over a
39-month period failed to reveal evidence of malignancy. The patient died
of an unrelated cause. Autopsy did not demonstrate any evidence of malignancy.
=============================================================
27.) Erythema gyratum repens.
=============================================================
Arch Dermatol 1985 Feb;121(2):170-1 Related Articles, Books
27.) Erythema gyratum repens.
=============================================================
Arch Dermatol 1985 Feb;121(2):170-1 Related Articles, Books
Levine LE, Morgan NE, Fretzin D, Rubenstein D
Publication Types:
Letter
=============================================================
=============================================================
28.) Gyrate erythema.
=============================================================
Dermatol Clin 1985 Jan;3(1):129-39 Related Articles, Books
Letter
=============================================================
=============================================================
28.) Gyrate erythema.
=============================================================
Dermatol Clin 1985 Jan;3(1):129-39 Related Articles, Books
White JW Jr
The gyrate erythemas consist of a nonspecific group (often called
erythema
annulare centrifugum) for which the cause is usually unknown, and three
specific types (erythema marginatum rheumaticum, erythema chronicum migrans
[Lyme disease], and erythema gyratum repens). The first specific type,
erythema marginatum rheumaticum, has become extremely rare with the decline
of its associated disease, rheumatic fever. The second specific type,
erythema chronicum migrans, is caused by a spirochete transmitted by the I.
ricinus complex of ticks. The third specific type, erythema gyratum repens,
is uncommon, morphologically distinctive, and an indicator of serious
disease, usually internal malignancy, in almost every instance.
annulare centrifugum) for which the cause is usually unknown, and three
specific types (erythema marginatum rheumaticum, erythema chronicum migrans
[Lyme disease], and erythema gyratum repens). The first specific type,
erythema marginatum rheumaticum, has become extremely rare with the decline
of its associated disease, rheumatic fever. The second specific type,
erythema chronicum migrans, is caused by a spirochete transmitted by the I.
ricinus complex of ticks. The third specific type, erythema gyratum repens,
is uncommon, morphologically distinctive, and an indicator of serious
disease, usually internal malignancy, in almost every instance.
=============================================================
29.) Infantile epidermodysplastic erythema gyratum responsive to imidazoles. A new entity?
=============================================================
Arch Dermatol 1984 Dec;120(12):1601-3 Related Articles, Books
29.) Infantile epidermodysplastic erythema gyratum responsive to imidazoles. A new entity?
=============================================================
Arch Dermatol 1984 Dec;120(12):1601-3 Related Articles, Books
Saurat JH, Janin-Mercier A
A 3 1/2-year-old girl had a three-year history of chronic annular
erythema
that more closely mimicked erythema gyratum repens of adults than other
annular erythemas of infancy. Histopathologic study revealed bowenoid
characteristics in the epidermis. No fungi were ever demonstrated in this
patient's skin lesions, but they consistently responded to treatment with
ketoconazole and flared immediately after cessation of treatment with that
drug.
that more closely mimicked erythema gyratum repens of adults than other
annular erythemas of infancy. Histopathologic study revealed bowenoid
characteristics in the epidermis. No fungi were ever demonstrated in this
patient's skin lesions, but they consistently responded to treatment with
ketoconazole and flared immediately after cessation of treatment with that
drug.
=============================================================
30.) Erythema gyratum repens with associated squamous cell carcinoma of the lung.
=============================================================
Cutis 1984 Oct;34(4):351-3, 355 Related Articles, Books
30.) Erythema gyratum repens with associated squamous cell carcinoma of the lung.
=============================================================
Cutis 1984 Oct;34(4):351-3, 355 Related Articles, Books
Olsen TG, Milroy SK, Jones-Olsen S
A 63-year-old man with erythema gyratum repens (EGR) was found to have
an
underlying squamous cell carcinoma of the lung. Neither radiation nor
chemotherapy had any effect on the extensive eruption. EGR is the most
distinctive of the figurate erythemas, and continues to be one of the most
consistent cutaneous signs of an associated visceral malignancy.
underlying squamous cell carcinoma of the lung. Neither radiation nor
chemotherapy had any effect on the extensive eruption. EGR is the most
distinctive of the figurate erythemas, and continues to be one of the most
consistent cutaneous signs of an associated visceral malignancy.
=============================================================
31.) [Cutaneous paraneoplastic syndromes].
=============================================================
Ann Med Interne (Paris) 1984;135(8):662-8 Related Articles, Books
31.) [Cutaneous paraneoplastic syndromes].
=============================================================
Ann Med Interne (Paris) 1984;135(8):662-8 Related Articles, Books
Barriere H
The authors list the really significant paraneoplastic cutaneous
syndromes:
acanthosis nigricans, paraneoplastic acrokeratosis, acquired ichthyosis
(and eventually the "explosive" onset of seborrheic warts) and a special
type of desquamative circinate erythema (erythema gyratum repens). The
possible paraneoplastic character of other conditions is also discussed:
dermatomyositis, necrosing vasculitis, autoimmune bullous conditions and
pruritus "sine materia".
acanthosis nigricans, paraneoplastic acrokeratosis, acquired ichthyosis
(and eventually the "explosive" onset of seborrheic warts) and a special
type of desquamative circinate erythema (erythema gyratum repens). The
possible paraneoplastic character of other conditions is also discussed:
dermatomyositis, necrosing vasculitis, autoimmune bullous conditions and
pruritus "sine materia".
=============================================================
32.) [Erythema gyratum repens and primary bronchial cancer. Disappearance of the dermatosis under general corticoid therapy].
=============================================================
Ann Dermatol Venereol 1983;110(4):329-34 Related Articles, Books
32.) [Erythema gyratum repens and primary bronchial cancer. Disappearance of the dermatosis under general corticoid therapy].
=============================================================
Ann Dermatol Venereol 1983;110(4):329-34 Related Articles, Books
[Article in French]
Larrouy JC, Apter J, Barety M, Ortonne JP
A case of Erythema Gyratum Repens in a 76 year old man with
bronchiolar
carcinoma is reported. The onset of the dermatosis preceded the discovery
of the neoplasm. Oral corticosteroids induced the disappearance of the skin
lesions. No recurrence was observed after discontinuation of the treatment.
The patient died 7 months after the onset of the dermatosis.
carcinoma is reported. The onset of the dermatosis preceded the discovery
of the neoplasm. Oral corticosteroids induced the disappearance of the skin
lesions. No recurrence was observed after discontinuation of the treatment.
The patient died 7 months after the onset of the dermatosis.
=============================================================
33.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
=============================================================
Med Cutan Ibero Lat Am 1983;11(4):281-6 Related Articles, Books
33.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
=============================================================
Med Cutan Ibero Lat Am 1983;11(4):281-6 Related Articles, Books
[Article in Spanish]
Yebra Sotillo I, Garcia Bravo B, Camacho Martinez F
A 65 year old male with Hodgkins disease, and generalised
figurate
Erythema, which during his period of hospitalisation migrated and became
much more evident, disappearing after initial therapy. Diagnosed as
"Erythema gyratum repens" reported by Gammel, an uncommon form of
paraneoplasic migrant figurate Erythema, we review the 33 previous cases of
this process, and find that, although 30 were related to other processes.
Erythema, which during his period of hospitalisation migrated and became
much more evident, disappearing after initial therapy. Diagnosed as
"Erythema gyratum repens" reported by Gammel, an uncommon form of
paraneoplasic migrant figurate Erythema, we review the 33 previous cases of
this process, and find that, although 30 were related to other processes.
=============================================================
34.) Erythema gyratum repens-like figurate eruption in bullous pemphigoid.
=============================================================
Clin Exp Dermatol 1982 Jul;7(4):401-6 Related Articles, Books
34.) Erythema gyratum repens-like figurate eruption in bullous pemphigoid.
=============================================================
Clin Exp Dermatol 1982 Jul;7(4):401-6 Related Articles, Books
Breathnach SM, Wilkinson JD, Black MM
=============================================================
=============================================================
35.) [Erythema gyratum repens].
=============================================================
Ugeskr Laeger 1979 Dec 17;141(51):3532 Related Articles, Books
=============================================================
35.) [Erythema gyratum repens].
=============================================================
Ugeskr Laeger 1979 Dec 17;141(51):3532 Related Articles, Books
[Article in Danish]
Christensen JD
=============================================================
=============================================================
36.) [Erythema gyratum repens].
=============================================================
Hautarzt 1979 Apr;30(4):213-5 Related Articles, Books
=============================================================
=============================================================
36.) [Erythema gyratum repens].
=============================================================
Hautarzt 1979 Apr;30(4):213-5 Related Articles, Books
[Article in German]
Verret JL, Schnitzler L, Schubert B, Alain YM, Bertrand G
A case of erythema gyratum repens is reported in 78 year old woman.
The
particularly typical eruption, mainly affecting the trunk, was associated
with a squamous cell carcinoma of the esophagus. The paraneoplastic
dermatosis cleared after radiotherapy of the cancer.
particularly typical eruption, mainly affecting the trunk, was associated
with a squamous cell carcinoma of the esophagus. The paraneoplastic
dermatosis cleared after radiotherapy of the cancer.
=============================================================
37.) Erythema gyratum repens: spontaneous resolution in a healthy man.
=============================================================
Br J Dermatol 1978 Oct;99(4):461 Related Articles, Books
37.) Erythema gyratum repens: spontaneous resolution in a healthy man.
=============================================================
Br J Dermatol 1978 Oct;99(4):461 Related Articles, Books
Stankler L
Publication Types:
Letter
=============================================================
=============================================================
38.) Erythema gyratum repens with pulmonary tuberculosis.
=============================================================
Br J Dermatol 1978 Apr;98(4):465-8 Related Articles, Books
Letter
=============================================================
=============================================================
38.) Erythema gyratum repens with pulmonary tuberculosis.
=============================================================
Br J Dermatol 1978 Apr;98(4):465-8 Related Articles, Books
Barber PV, Doyle L, Vickers DM, Hubbard H
A 63-year-old man presented with erythema gyratum repens of 7
months'
duration. A cavitating mass at the right lung apex was resected and proved
to be tuberculous. Following the resection, the skin lesions cleared within
a few days. Erythema gyratum repens has not previously been described in
association with non-malignant visceral pathology. The pathogenesis remains
obscure but cannot be related specifically to a response to tumour cells or
their products in view of the association reported here. The condition
bears no resemblance to any known tuberculide.
duration. A cavitating mass at the right lung apex was resected and proved
to be tuberculous. Following the resection, the skin lesions cleared within
a few days. Erythema gyratum repens has not previously been described in
association with non-malignant visceral pathology. The pathogenesis remains
obscure but cannot be related specifically to a response to tumour cells or
their products in view of the association reported here. The condition
bears no resemblance to any known tuberculide.
=============================================================
39.) [Gammel's erythema gyratum repens and acquired ichthyosis associated with esophageal carcinoma].
=============================================================
Ann Dermatol Venereol 1978 Mar;105(3):319-21 Related Articles, Books
39.) [Gammel's erythema gyratum repens and acquired ichthyosis associated with esophageal carcinoma].
=============================================================
Ann Dermatol Venereol 1978 Mar;105(3):319-21 Related Articles, Books
Barriere H, Litoux P, Bureau B, Preel JL, Thebaud Y
=============================================================
=============================================================
=============================================================
40.) [Erythema gyratum repens or Gammel paraneoplastic syndrome. A case with
epidermoid carcinoma developed on a megaesophagus].
=============================================================
Ann Dermatol Venereol 1977 May;104(5):403-6 Related Articles, Books
40.) [Erythema gyratum repens or Gammel paraneoplastic syndrome. A case with
epidermoid carcinoma developed on a megaesophagus].
=============================================================
Ann Dermatol Venereol 1977 May;104(5):403-6 Related Articles, Books
[Article in French]
Verret JL, Pierrin B, Bertrand G, Dubin J, Allain YM, Schnitzler
L
=============================================================
=============================================================
41.) Erythema gyratum repens--an immunologically mediated dermatosis?
=============================================================
Br J Dermatol 1977 Apr;96(4):343-7 Related Articles, Books
41.) Erythema gyratum repens--an immunologically mediated dermatosis?
=============================================================
Br J Dermatol 1977 Apr;96(4):343-7 Related Articles, Books
Holt PJ, Davies MG
=============================================================
=============================================================
=============================================================
42.) Erythema gyratum repens with metastatic adenocarcinoma.
=============================================================
Arch Dermatol 1975 Feb;111(2):227-9 Related Articles, Books
42.) Erythema gyratum repens with metastatic adenocarcinoma.
=============================================================
Arch Dermatol 1975 Feb;111(2):227-9 Related Articles, Books
Skolnick M, Mainman ER
A patient with Erythema Gyratum Repens (EGR) had a marked increase of
his
eruption, with uncontrollable pruritus that was unresponsive to steriod
therapy. This culminated in an exfoliative dermatitis. A metastatic,
undifferentiated adenocarcinoma was removed following a right-sided
craniotomy. The patient then had complete cessation of his pruritus, with
moderate improvement of his eruption. All the reported cases of EGR were
reviewed in terms of the source of the malignant disorder. The relationship
between the time of onset of the EGR and the discovery of the malignant
disorder, as well as the effect of treatment of the malignant condition on
the course of the EGR, was studied. The data suggest a highly probable
relationship between the two.
eruption, with uncontrollable pruritus that was unresponsive to steriod
therapy. This culminated in an exfoliative dermatitis. A metastatic,
undifferentiated adenocarcinoma was removed following a right-sided
craniotomy. The patient then had complete cessation of his pruritus, with
moderate improvement of his eruption. All the reported cases of EGR were
reviewed in terms of the source of the malignant disorder. The relationship
between the time of onset of the EGR and the discovery of the malignant
disorder, as well as the effect of treatment of the malignant condition on
the course of the EGR, was studied. The data suggest a highly probable
relationship between the two.
=============================================================
43.) [Erythema gyratum repens (Gammel's syndrome)]
=============================================================
SO - Hautarzt 1979 Apr;30(4):213-5
AU - Verret JL; Schnitzler L; Schubert B; Alain YM; Bertrand G
PT - JOURNAL ARTICLE
AB - A case of erythema gyratum repens is reported in 78 year old woman.
The particularly typical eruption, mainly affecting the trunk, was
associated with a squamous cell carcinoma of the esophagus. The
paraneoplastic dermatosis cleared after radiotherapy of the cancer.
43.) [Erythema gyratum repens (Gammel's syndrome)]
=============================================================
SO - Hautarzt 1979 Apr;30(4):213-5
AU - Verret JL; Schnitzler L; Schubert B; Alain YM; Bertrand G
PT - JOURNAL ARTICLE
AB - A case of erythema gyratum repens is reported in 78 year old woman.
The particularly typical eruption, mainly affecting the trunk, was
associated with a squamous cell carcinoma of the esophagus. The
paraneoplastic dermatosis cleared after radiotherapy of the cancer.
=============================================================
44.) Figurate and bullous eruption in association with breast carcinoma.
=============================================================
44.) Figurate and bullous eruption in association with breast carcinoma.
=============================================================
SO - Arch Dermatol 1990 May;126(5):649-52
AU - Watsky KL; Orlow SJ; Bolognia JL
PT - JOURNAL ARTICLE; REVIEW (16 references); REVIEW OF REPORTED CASES
AB - We describe a patient with two coexistent cutaneous eruptions: (1)
trauma-induced bullae of the distal extremities and elbows and (2) multiple
concentric gyrate lesions on the trunk and extremities, some of which
became bullous. The gyrate lesions were stationary and nonpruritic. Biopsy
of both types of lesions showed a subepidermal blister and a minimal
inflammatory infiltrate. Direct immunofluorescence revealed linear
deposition of IgG and C3 at the dermoepidermal junction and indirect
immunofluorescence was negative. By immunoelectron microscopy, these immune
deposits were localized to the lower lamina lucida. The eruption was not
controlled despite high-dose (80 mg/d) oral administration of prednisone
and required the addition of an oral administration of methotrexate (20 mg
weekly). On further evaluation, an intraductal mammary carcinoma was
detected. Following radiation therapy, the methotrexate and prednisone
therapy were tapered without recurrence of the eruption during a follow-up
period of 18 months.
AU - Watsky KL; Orlow SJ; Bolognia JL
PT - JOURNAL ARTICLE; REVIEW (16 references); REVIEW OF REPORTED CASES
AB - We describe a patient with two coexistent cutaneous eruptions: (1)
trauma-induced bullae of the distal extremities and elbows and (2) multiple
concentric gyrate lesions on the trunk and extremities, some of which
became bullous. The gyrate lesions were stationary and nonpruritic. Biopsy
of both types of lesions showed a subepidermal blister and a minimal
inflammatory infiltrate. Direct immunofluorescence revealed linear
deposition of IgG and C3 at the dermoepidermal junction and indirect
immunofluorescence was negative. By immunoelectron microscopy, these immune
deposits were localized to the lower lamina lucida. The eruption was not
controlled despite high-dose (80 mg/d) oral administration of prednisone
and required the addition of an oral administration of methotrexate (20 mg
weekly). On further evaluation, an intraductal mammary carcinoma was
detected. Following radiation therapy, the methotrexate and prednisone
therapy were tapered without recurrence of the eruption during a follow-up
period of 18 months.
=============================================================
45.) [Erythema gyratum repens associated with bronchial carcinoma]
=============================================================
SO - Hautarzt 1970 Mar;21(3):116-9
AU - Hochleitner H; Bartsch G; Zelger J
PT - JOURNAL ARTICLE
=============================================================
=============================================================
46.) Erythema gyratum repens. Reports of two further cases associated with
carcinoma.
=============================================================
SO - Br J Dermatol 1970 Apr;82(4):406-11
AU - Thomson J; Stankler L
PT - JOURNAL ARTICLE
=============================================================
=============================================================
47.) Carcinoma of the breast, pemphigus vulgaris and gyrate erythema.
=============================================================
SO - Int J Dermatol 1978 Apr;17(3):221-4
AU - Jacobs R; Eng AM; Solomon LM
PT - JOURNAL ARTICLE
=============================================================
45.) [Erythema gyratum repens associated with bronchial carcinoma]
=============================================================
SO - Hautarzt 1970 Mar;21(3):116-9
AU - Hochleitner H; Bartsch G; Zelger J
PT - JOURNAL ARTICLE
=============================================================
=============================================================
46.) Erythema gyratum repens. Reports of two further cases associated with
carcinoma.
=============================================================
SO - Br J Dermatol 1970 Apr;82(4):406-11
AU - Thomson J; Stankler L
PT - JOURNAL ARTICLE
=============================================================
=============================================================
47.) Carcinoma of the breast, pemphigus vulgaris and gyrate erythema.
=============================================================
SO - Int J Dermatol 1978 Apr;17(3):221-4
AU - Jacobs R; Eng AM; Solomon LM
PT - JOURNAL ARTICLE
=============================================================
=============================================================
48.) [Premycotic erythema simulating erythema gyratum repens].
=============================================================
Bull Soc Fr Dermatol Syphiligr 1969;76(1):12 Related Articles, Books
48.) [Premycotic erythema simulating erythema gyratum repens].
=============================================================
Bull Soc Fr Dermatol Syphiligr 1969;76(1):12 Related Articles, Books
[Article in French]
Duperrat B, Puissant A, Cherif-Cheikh JL, Pringuet R, David V, Blanchet
P
=============================================================
=============================================================
=============================================================
=============================================================
=============================================================
49.) An unusual paraneoplastic syndrome: erythema "gyratum repens" or Gammel's syndrome].
=============================================================
Presse Med 1967 May 20;75(24):1239-42 Related Articles, Books
49.) An unusual paraneoplastic syndrome: erythema "gyratum repens" or Gammel's syndrome].
=============================================================
Presse Med 1967 May 20;75(24):1239-42 Related Articles, Books
[Article in French]
Migueres J, Jover A, Layssol M, Ranfaing J
=============================================================
=============================================================
50.) [An unusual paraneoplastic syndrome: erythema gyratum repens. Its relation with bronchial cancer].
=============================================================
J Fr Med Chir Thorac 1967 Apr;21(3):313-24 Related Articles, Books
=============================================================
50.) [An unusual paraneoplastic syndrome: erythema gyratum repens. Its relation with bronchial cancer].
=============================================================
J Fr Med Chir Thorac 1967 Apr;21(3):313-24 Related Articles, Books
[Article in French]
Migueres J, Jover A, Layssol M, Ranfaing J
=====================================51.) Cutaneous manifestations of lung cancer.
=====================================
Owen CE1.
Author information
1University of Louisville, Division of Dermatology, Louisville, KY. Electronic address: ceowen01@louisville.edu.
Abstract
Skin findings can serve as a clue to internal disease. In this article, cutaneous manifestations of underlying lung malignancy are reviewed. Paraneoplastic dermatoses are rare, but when recognized early, can lead to early diagnosis of an underlying neoplasm. Malignancy-associated dermatoses comprise a broad group of hyperproliferative and inflammatory disorders, disorders caused by tumor production of hormonal or metabolic factors, autoimmune connective tissue diseases, among others. In this review, paraneoplastic syndromes associated with lung malignancy are discussed, including ectopic ACTH syndrome, bronchial carcinoid variant syndrome, secondary hypertrophic osteoarthropathy/digital clubbing, erythema gyratum repens, malignant acanthosis nigricans, sign of Leser-Trélat, tripe palms, hypertrichosis lanuginosa, acrokeratosis paraneoplastica, and dermatomyositis.
=========================================
52.) Cutaneous manifestations of breast cancer.
========================================
Semin Oncol. 2016 Jun;43(3):331-4. doi: 10.1053/j.seminoncol.2016.02.030. Epub 2016 Feb 23.
Tan AR1.
Author information
1Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC. Electronic address: Antoinette.Tan@CarolinasHealthcare.org.
Abstract
Breast cancer may present with cutaneous symptoms. The skin manifestations of breast cancer are varied. Some of the more common clinical presentations of metastatic cutaneous lesions from breast cancer will be described. Paraneoplastic cutaneous dermatoses have been reported as markers of breast malignancy and include erythema gyratum repens, acquired ichthyosis, dermatomyositis, multicentric reticulohistiocytosis, and hypertrichosis lanuginosa acquisita. Mammary Paget's disease, often associated with an underlying breast cancer, and Cowden syndrome, which has an increased risk of breast malignancy, each have specific dermatologic findings. Recognition of these distinct cutaneous signs is important in the investigation of either newly diagnosed or recurrent breast cancer.
=========================================
53.) Erythema gyratum repens.
========================================
Eubanks LE1, McBurney E, Reed R.
Author information
1Department of Dermatology, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Abstract
BACKGROUND:
Erythema gyratum repens is a rare, clinically specific, and distinctive paraneoplastic syndrome. It is associated with internal malignancy in 82% of patients.
OBJECTIVE:
A 58-year-old man with erythema gyratum repens is described. On diagnosis of his eruption, a malignancy work-up revealed a 9-mm pulmonary adenocarcinoma. Removal of the carcinoma resulted in clearing of the erythema.
RESULTS:
Erythema gyratum repens is most commonly associated with bronchial, esophageal, and breast cancer. It has also rarely been reported in patients without evidence of malignancy. The histopathologic findings are nonspecific. Direct immunofluorescence has sometimes revealed C3, C4, or immunoglobulin G at the basement membrane zone.
CONCLUSION:
The etiology of erythema gyratum repens is unknown, although an immune response is postulated. Treatment involves treating the underlying malignancy.
=============================================
54.) Erythema gyratum repens unassociated with underlying malignancy.
============================================
J Dermatol. 1995 Aug;22(8):587-9.
Kawakami T1, Saito R.
Author information
1Second Department of Dermatology, Toho University School of Medicine, Tokyo, Japan.
Abstract
A case of erythema gyratum repens occurring in a 62-year-old woman is presented together with a review of the literature. Evaluation and follow-up for the development of malignancy over a 32-month period failed to reveal any evidence of malignancy. Formerly, all cases of erythema gyratum repens were evaluated in terms of an association with an underlying malignant disorder. To date, only sixty cases have been reported in the literature; 14 (23%) were not found to be associated with any neoplasm. Therefore, this term is now also used for cases unassociated with malignancy. Erythema gyratum repens is a cutaneous eruption with a characteristic diagnostic morphology resembling a wood grain pattern.
============================================
55.) Erythema gyratum repens unassociated with internal malignancy.
============================================
J Am Acad Dermatol. 1985 May;12(5 Pt 2):911-3.
Langlois JC, Shaw JM, Odland GF.
Abstract
A case report of erythema gyratum repens occurring in a 68-year-old man is presented. Evaluation and follow-up for development of malignancy over a 39-month period failed to reveal evidence of malignancy. The patient died of an unrelated cause. Autopsy did not demonstrate any evidence of malignancy.
===========================================
56.) Erythema gyratum repens associated with cryptogenic organizing pneumonia.
==========================================
Indian J Dermatol Venereol Leprol. 2016 Mar-Apr;82(2):212-3. doi: 10.4103/0378-6323.173594.
Samotij D, Szczech J, Bencal-Kusinska M, Reich A1.
Author information
1Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Wroclaw, Poland.
============================================
57.) Erythema gyratum repens preceding the onset of rheumatoid arthritis.
===========================================
Eur J Dermatol. 2013 May-Jun;23(3):399-400. doi: 10.1684/ejd.2013.2049.
Endo Y1, Fujisawa A1, Tanioka M1, Miyachi Y1.
Author information
1Department of Dermatology, Kyoto University, 54 Shogoin-Kawara-cho, Sakyo, Kyoto 606-8507, Japan.
=============================================
58.) Erythema gyratum repens associated with hypereosinophilic syndrome.
=============================================
J Dermatol. 1994 Aug;21(8):612-4.
Morita A1, Sakakibara N, Tsuji T.
Author information
Abstract
We report a case of typical erythema gyratum repens lesions observed as a manifestation of idiopathic hypereosinophilic syndrome in a 63-year-old man. While erythema gyratum repens is usually associated with malignancy, an intensive search over a 30-month period failed to reveal any evidence of neoplasm. With administration of dapsone, the typical gyrate lesions disappeared as the subject's hypereosinophilia improved.
==============================================
59.) [Erythema gyratum repens of Gammel and Hodgkin's disease].
===============================================
Med Cutan Ibero Lat Am. 1983;11(4):281-6.
[Article in Spanish]
Yebra Sotillo I, Garciá Bravo B, Camacho Martínez F.
Abstract
A 65 year old male with Hodgkins disease, and generalised figurate Erythema, which during his period of hospitalisation migrated and became much more evident, disappearing after initial therapy. Diagnosed as "Erythema gyratum repens" reported by Gammel, an uncommon form of paraneoplasic migrant figurate Erythema, we review the 33 previous cases of this process, and find that, although 30 were related to other processes.
=============================================
60.) Erythema gyratum repens is not an obligate paraneoplastic disease: a systematic review of the literature and personal experience.
=============================================
J Eur Acad Dermatol Venereol. 2014 Jan;28(1):112-5. doi: 10.1111/j.1468-3083.2012.04663.x. Epub 2012 Jul 25.
Rongioletti F1, Fausti V, Parodi A.
Author information
1Section of Dermatology, DISSAL, University of Genoa, Genoa, Italy.
Abstract
BACKGROUND:
Erythema gyratum repens (EGR) is a rare clinical entity that is considered to be an obligatory paraneoplastic disease. According to the literature, an underlying neoplasm can be detected in 82% of the cases.
OBJECTIVES:
The aim of this systemic review was to evaluate the association of EGR with malignancies or other non-neoplastic conditions.
METHODS:
The medical records of patients seen at the Section of Dermatology, University of Genoa between 1990 and 2010, in whom a diagnosis of EGR had been made, were reviewed for evidence of systemic associations. A systematic search of the Cochrane library, EMBASE, Pubmed and MEDLINE databases was also conducted. Key search term used in the review was 'erythema gyratum repens'.
RESULTS:
Four patients with a diagnosis of EGR have been retrieved from our medical records. One case was idiopathic, one was associated with a bronchial carcinoma and two were associated with drug-intake. One hundred and twelve original cases of EGR were selected from the literature for detailed review. Among these, 58 cases (70%) were associated with an underlying neoplasm, 25 cases (30%) were non-paraneoplastic and 29 cases have been considered as different dermatoses mimicking EGR in their clinical presentation ('EGR-like' eruption).
CONCLUSION:
EGR should no longer be considered as an obligate paraneoplastic syndrome as the cases that are not associated with neoplasm are more than expected. In addition to searching an underlying neoplasm, dermatologists should be aware about the possibility of other associations including also drug-intake.
=============================================
61.) Novel presentation of lepromatous leprosy in an erythema gyratum repens-like pattern.
=============================================
Int J Dermatol. 2014 Feb;53(2):210-2. doi: 10.1111/ijd.12237. Epub 2013 Dec 10.
Mohanan S1, Devi AS, Kumari R, Thappa DM, Ganesh RN.
Author information
1Department of Skin and Sexually Transmitted Diseases, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Abstract
OBJECTIVES:
Leprosy can have diverse cutaneous and occasionally perplexing presentations. We report an unusual case of lepromatous leprosy (LL) with annular lesions resembling erythema gyratum repens.
REPORT:
A 55-year-old man presented with a symmetrical, hypopigmented, and erythematous rash of bizarre appearance over the lateral aspect of the upper arm, and anterior and posterior aspects of the trunk of two months' duration. He gave a history of self-resolving episodes of bilateral pedal edema, and numbness and pricking sensations in both the hands and feet, which had occurred intermittently over the previous six years. An ulcer measuring 2 cm in size was present over the adjacent surface of the right first and second toes. The bilateral ulnar and radial cutaneous nerves were symmetrically thickened.
RESULTS:
Slit-skin smears revealed numerous acid-fast bacilli. Skin biopsy from the trunk showed collections of histiocytes, lymphocytes, and plasma cells in the dermis and around the blood vessels. The patient was diagnosed with LL and started on multibacillary multi-drug therapy.
CONCLUSIONS:
Lepromatous leprosy can have varied clinical manifestations and is often a great imitator. However, the skin smear positivity, even in normal skin, symmetrical cutaneous and peripheral nerve involvement, and histopathology in the present patient were indicative of LL. This report highlights a rare presentation of leprosy. Clinicians should be aware of these rare manifestations as lepromatous cases still occur in certain regions.
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62.) Leucocytoclastic vasculitis presenting as an erythema gyratum repens-like eruption.
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Clin Exp Dermatol. 2016 Apr;41(3):320-2. doi: 10.1111/ced.12749. Epub 2015 Sep 3.
Spierings NM1, Natkunarajah J2.
Author information
1Dermatology Department, Ground Floor, Lanesborough Wing, St. George's Hospital NHS Trust, Blackshaw Road, London, SW17 0QT, UK. nspierings@doctors.org.uk.
2Dermatology Department, Kingston Hospital NHS Trust, London, UK.
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63.) Urticarial vasculitis presenting as erythema gyratum repens-like eruption.
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Noda S, Takekoshi T, Tamaki Z, Asano Y, Sugaya M, Sato S.
J Eur Acad Dermatol Venereol. 2011 Apr;25(4):493-5. doi: 10.1111/j.1468-3083.2010.03747.x.
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64.) Erythema gyratum repens-like eruption occuring in resolving psoriasis during methotrexate therapy.
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Int J Dermatol. 2010 Mar;49(3):306-7. doi: 10.1111/j.1365-4632.2009.04256.x.
Singal A1, Sonthalia S, Pandhi D.
Author information
1Department of Dermatology and STD, University College of Medical Sciences and GTB Hospital, University of Delhi, New Delhi, India.
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65.) Erythema gyratum repens-like eruption in a patient with epidermolysis bullosa acquisita
associated with ulcerative colitis.
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Br J Dermatol. 2007 Apr;156(4):773-5. Epub 2007 Jan 30.
España A, Sitaru C, Pretel M, Aguado L, Jimenez J.
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66.) Erythema gyratum repens-like eruption in mycosis fungoides: is dermatophyte superinfection
underdiagnosed in cutaneous T-cell lymphomas?
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J Eur Acad Dermatol Venereol. 2008 Nov;22(10):1276-8. doi: 10.1111/j.1468-3083.2008.02628.x. Epub 2008 Mar 7.
Jouary T, Lalanne N, Stanislas S, Vergier B, Delaunay M, Taieb A.
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67.) Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.
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Landau M1, Cohen-Bar-Dayan M, Hohl D, Ophir J, Wolf CR, Gat A, Mevorah B.
Author information
1Dermatology Unit, Edith Wolfson Medical Center, Holon, Israel, Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel. landau@post.tau.ac.il
Abstract
A large pedigree with erythrokeratodermia variabilis (EKV) and erythema gyratum repens-like lesions is described. Clinical, laboratory, and histologic findings of this family are presented. The differential diagnoses of the following dermatoses with an erythematous and a hyperkeratotic component are discussed: erythrokeratodermia variabilis (Mendes da Costa), progressive symmetric erythrokeratoderma (Gottron), loricrin keratoderma, erythrokeratoderma en cocardes (Degos), Netherton syndrome, keratitis-ichthyosis-deafness (KID) syndrome, erythrokeratolysis hiemalis (Oudtshoorn disease), and nonbullous congenital ichthyosiform erythroderma.
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68.) Erythema gyratum repens-like eruption in a patient with Sjögren syndrome.
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Acta Derm Venereol. 1995 Jul;75(4):327.
Matsumura T, Kumakiri M, Sato-Matsumura KC, Ohkawara A.
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69.) Neutrophilic dermatosis with an erythema gyratum repens-like pattern in systemic lupus erythematosus.
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Acta Derm Venereol. 2005;85(5):455-6.
Khan Durani B, Andrassy K, Hartschuh W.
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70.) Penicillin-induced anti-p200 pemphigoid: an unusual morphology.
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Acta Derm Venereol. 2006;86(5):443-6.
Wozniak K1, Kowalewski C, Hashimoto T, Ishii N, Glinska-Wielochowska M, Schwartz RA.
Author information
1Department of Dermatology, Medical University of Warsaw, PL-02008 Warsaw, Poland. kwoznia@amwaw.edu.pl
Abstract
We report here a case of a 52-year-old woman with erythema gyratum repens-like lesions appearing during anti-p200 pemphigoid, probably induced by oral penicillin. The diagnosis of anti-p200 pemphigoid was made by the presence of in vivo bound and circulating IgG anti-basement membrane zone auto-antibody reactive with the dermal side of salt-split skin and with 200 kDa protein in dermal extract on Western immunoblot. Laser scanning confocal microscopic study disclosed the localization of IgG at the lamina lucida-lamina densa border. Skin lesions responded poorly to high dose of prednisone and the combination of prednisone and dapsone. When methotrexate was added, skin lesions healed within 3 weeks. To our knowledge, erythema gyratum repens-like lesions have not been described previously in this disorder. Thus, we have expanded the clinical morphological spectrum of patients with anti-p200 pemphigoid and first described a patient whose disorder was probably drug-induced.
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