Sneddon-Wilkinson disease: a case report

被引：0

作者：

Kerroum, Sara ^{[1
]}

Ammar, Najoua ^{[1
]}

Znati, Kaoutar ^{[2
]}

Ismaili, Nadia ^{[1
]}

Meziane, Mariame ^{[1
]}

Benzekri, Laila ^{[1
]}

Senouci, Karima ^{[1
]}

机构：

[1] Univ Mohammed 5, Fac Med & Pharm, Ctr Hosp Univ Ibn Sina, Serv Dermatol Venerol, Rabat, Morocco

[2] Univ Mohammed 5, Fac Med Pharm, Ctr Hosp Univ Ibn Sina, Serv Anatomopathol, Rabat, Morocco

来源：

PAN AFRICAN MEDICAL JOURNAL | 2022年 / 43卷

关键词：

Subcorneal pustulosis (Sneddon-Wilkinson disease); dapsone; case report;

D O I：

10.11604/pamj.2022.43.115.33116

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

Sneddon-Wilkinson disease is a benign amicrobial pustulosis belonging to the spectrum of neutrophilic dermatoses. It is characterized by evident stereotypic clinical features, including, in most cases, pustular lesions of the trunk and prominent skin folds. This pustulosis may be associated with other diseases (IgA monoclonal gammopathy, rheumatoid arthritis, neoplasms or other neutrophilic dermatoses) and therefore requires regular follow-up. This disease has a relapsing-remitting course. First line therapy is dapsone. We here report the case of a 49-year-old patient with amicrobial pustulosis (Sneddon-Wilkinson disease).

引用

页数：6

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