Amicrobial pustulosis associated with autoimmune disease in a patient with Sjogren syndrome and IgA nephropathy

被引：8

作者：

Lim, Y. L. ^{[1
]}

Ng, S. K. ^{[1
]}

Lian, T. Y. ^{[2
]}

机构：

[1] Natl Skin Ctr, Singapore 308205, Singapore

[2] Tan Tock Seng Hosp, Dept Rheumatol, Singapore, Singapore

来源：

CLINICAL AND EXPERIMENTAL DERMATOLOGY | 2012年 / 37卷 / 04期

关键词：

LUPUS-ERYTHEMATOSUS; FOLDS;

D O I：

10.1111/j.1365-2230.2011.04262.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Amicrobial pustulosis associated with autoimmune disease (APAD) is a rare clinical condition, characterized by relapsing pustular eruption, affecting mainly the skin folds. Almost all previously described cases were young women with varying underlying autoimmune diseases. We report a 36-year-old woman with the interesting triad of APAD, Sjogren syndrome and IgA nephropathy. Her rashes responded to oral prednisolone and cyclophosphamide.

引用

页码：374 / 378

页数：5

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