Literature DB >> 3734185

Malignant atrophic papulosis: absence of circulating immune complexes or vasculitis.

K Tribble, M E Archer, J L Jorizzo, R Sanchez, A R Solomon, F H Gardner, T Cavallo.   

Abstract

A 26-year-old woman presented with the classic manifestations of malignant atrophic papulosis, a rare disease of unknown cause. We report the results of our immunologic studies, which may help to explain why treatment with systemic immunosuppressant therapy has not been effective.

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Year:  1986        PMID: 3734185     DOI: 10.1016/s0190-9622(86)70180-1

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  4 in total

1.  Degos disease - malignant atrophic papulosis or cutaneointestinal lethal syndrome: rarity of the disease.

Authors:  Eduardo Pirolla; Felipe Fregni; Irene K Miura; Antonio Carlos Misiara; Fernando Almeida; Esdras Zanoni
Journal:  Clin Exp Gastroenterol       Date:  2015-04-16

2.  Two cases of Degos disease with different prognosis.

Authors:  Zhiliang Li; Peiying Jin; Baoxi Wang; Suying Feng
Journal:  Postepy Dermatol Alergol       Date:  2014-12-03       Impact factor: 1.837

3.  Degos Disease (Malignant Atrophic Papulosis) With Granular IgM on Direct Immunofluorescence.

Authors:  Tatsiana Pukhalskaya; Julia Stiegler; Glynis Scott; Christopher T Richardson; Bruce Smoller
Journal:  Cureus       Date:  2021-01-13

Review 4.  Malignant atrophic papulosis (Köhlmeier-Degos disease) - a review.

Authors:  Athanasios Theodoridis; Evgenia Makrantonaki; Christos C Zouboulis
Journal:  Orphanet J Rare Dis       Date:  2013-01-14       Impact factor: 4.123

  4 in total

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