Lupus érythémateux systémique se présentant comme un syndrome de Stevens-Johnson

S. Bellakhal, B. Ben Kaab, Z. Teyeb, A. Souissi, F. Derbel, M.-H. Douggui
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引用次数: 2

Abstract

Stevens-Johnson syndrome and toxic epidermal necrolysis are life-threatening dermatological conditions. Their most common cause is medication. However, in a small proportion of patients these dermatological conditions could be the first presentation of systemic lupus erythematosus. We now describe a 34-year-old patient who presented with manifestations of Stevens-Johnson as a first feature of systemic lupus erythematosus. Systemic lupus erythematosus reveled by Stevens-Johnson syndrome has been infrequently reviewed in the previous literature. This diagnosis should be considered when cutaneous adverse drug reactions occur without clear drug causality.

系统性红斑狼疮表现为史蒂文-约翰逊综合征
史蒂文斯-约翰逊综合征和中毒性表皮坏死松解是危及生命的皮肤病。最常见的原因是药物治疗。然而,在一小部分患者中,这些皮肤病可能是系统性红斑狼疮的首次表现。我们现在描述一个34岁的病人谁提出史蒂文斯-约翰逊的表现作为系统性红斑狼疮的第一个特征。史蒂文斯-约翰逊综合征引起的系统性红斑狼疮在以前的文献中很少被回顾。当皮肤药物不良反应没有明确的药物因果关系时,应考虑此诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathologie-biologie
Pathologie-biologie 医学-病理学
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6-12 weeks
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