Literature DB >> 10550360

[Intertriginous acantholytic dyskeratosis: abortive form of Darier disease or a specific entity?].

M Leverkus1, C Rose, E B Bröcker, H Hamm.   

Abstract

A 69-year-old woman presented with widespread symmetrical papular lesions in submammary and inguinal areas. History revealed that the disease had only been present for a few years. A skin biopsy showed focal suprabasal acantholysis, dyskeratosis up to the horny layer and in part parakeratotic hyperkeratosis. The patient had no further evidence for Darier disease, Hailey-Hailey disease or pemphigus vegetans. In particular, characteristic lesions of Darier disease of hands and nails were absent. We found several reports in the literature describing similar skin lesions in intertriginous and genital areas with histological evidence of acantholytic dyskeratosis under various terms. This report discusses the difference between these cases and the differential diagnoses, in particular Darier disease. We propose to designate cases of intertriginous papulosis with histological proof of acantholytic dyskeratosis but without further evidence of Darier disease as intertriginous acantholytic dyskeratosis.

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Year:  1999        PMID: 10550360     DOI: 10.1007/s001050051059

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  1 in total

1.  Somatic ATP2A2 mutation in a case of papular acantholytic dyskeratosis: mosaic Darier disease.

Authors:  Eleanor A Knopp; Corey Saraceni; Jeremy Moss; Jennifer M McNiff; Keith A Choate
Journal:  J Cutan Pathol       Date:  2015-08-12       Impact factor: 1.587

  1 in total

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