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甲氧苄啶-磺胺甲恶唑相关急性发热性嗜中性皮病:病例报告及药物性Sweet综合征综述

Trimethoprim-sulfamethoxazole-associated acute febrile neutrophilic dermatosis: case report and review of drug-induced Sweet's syndrome.

作者信息

Walker D C, Cohen P R

机构信息

Department of Dermatology, University of Texas-Houston Medical School 77030, USA.

出版信息

J Am Acad Dermatol. 1996 May;34(5 Pt 2):918-23. doi: 10.1016/s0190-9622(96)90080-8.

Abstract

Sweet's syndrome, or acute febrile neutrophilic dermatosis, is characterized by fever, neutrophilia, and painful erythematous cutaneous plaques that contain a dense neutrophilic dermal infiltrate. Although the disorder is usually idiopathic, patients with drug-induced Sweet's syndrome have been described. We describe a 50-year-old woman with trimethoprim-sulfamethoxazole (TMP-SMX)--induced Sweet's syndrome and review the features of the 13 previously reported patients with drug-induced Sweet's syndrome. All patients had fever, painful skin lesions (most commonly on the upper extremities), and a biopsy-confirmed neutrophilic dermatosis. All patients also exhibited a temporal relationship between drug administration and clinical presentation and between drug withdrawal and healing. In patients with drug-induced Sweet's syndrome, neutrophilia is often absent.

摘要

斯威特综合征,即急性发热性嗜中性皮病,其特征为发热、嗜中性粒细胞增多,以及疼痛性红斑皮肤斑块,斑块内有密集的嗜中性粒细胞真皮浸润。尽管该病症通常为特发性,但也有药物诱发斯威特综合征的患者报道。我们描述了一名50岁女性,她患有甲氧苄啶-磺胺甲恶唑(TMP-SMX)诱发的斯威特综合征,并回顾了之前报道的13例药物诱发斯威特综合征患者的特征。所有患者均有发热、疼痛性皮肤病变(最常见于上肢),且活检证实为嗜中性皮病。所有患者在用药与临床表现之间以及停药与愈合之间也都呈现出时间关系。在药物诱发斯威特综合征的患者中,常无嗜中性粒细胞增多。

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