Sneddon-Wilkinson disease treated with etanercept: report of two cases

被引：18

作者：

Berk, D. R. ^{[1
]}

Hurt, M. A. ^{[2
]}

Mann, C. ^{[1
]}

Sheinbein, D. ^{[1
]}

机构：

[1] Washington Univ, Sch Med, Div Dermatol, Dept Internal Med, St Louis, MO 63110 USA

[2] WCP Labs Inc, Cutaneous Pathol, Maryland Hts, MO USA

来源：

CLINICAL AND EXPERIMENTAL DERMATOLOGY | 2009年 / 34卷 / 03期

关键词：

SUBCORNEAL PUSTULAR DERMATOSIS; NECROSIS-FACTOR-ALPHA;

D O I：

10.1111/j.1365-2230.2008.02905.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Sneddon-Wilkinson disease (SWD), also known as subcorneal pustular dermatosis, is a rare, chronic eruption that is often difficult to treat, particularly in patients who do not respond to or cannot tolerate dapsone. Few case reports exist of patients with SWD treated with antitumour necrosis factor-alpha therapy. We report two patients with SWD refractory to numerous treatments, who responded to etanercept (in combination with low-dose acitretin in one case).

引用

页码：347 / 351

页数：5

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