Hoch O, Herbst R A, Gutzmer R, Kiehl P, Kapp A, Weiss J
Dermatologische Klinik und Poliklinik, Medizinischen Hochschule Hannover.
Hautarzt. 1998 Aug;49(8):634-40. doi: 10.1007/s001050050800.
During the last decade an unusual amicrobial intertriginous pustulosis has been described in association with autoimmune disease in sixteen female patients. The clinical hallmark is a sterile pustular dermatosis preferentially located in intertriginous regions that responds to local or systemic corticosteroids. Histologic features are subcorneal sometimes spongiform neutrophilic pustules. We report an additional patient suffering from this unusual dermatosis. An overview of the patients described to date and a review of the literature are given in an attempt to delineate this amicrobial intertriginous pustulosis from the known pustular dermatoses.
在过去十年中,已报道了16例女性患者患有一种与自身免疫性疾病相关的罕见无菌性擦烂性脓疱病。临床特征为无菌性脓疱性皮肤病,好发于擦烂部位,对局部或全身性皮质类固醇治疗有效。组织学特征为角层下有时为海绵状嗜中性脓疱。我们报告了另外一名患有这种罕见皮肤病的患者。本文对迄今为止报道的患者进行了概述,并对文献进行了综述,旨在将这种无菌性擦烂性脓疱病与已知的脓疱性皮肤病区分开来。