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万古霉素诱发的线性IgA大疱病表现为中毒性表皮坏死松解症
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作者 Waldman M.A. black d.r. +1 位作者 Callen J.P. 王琼 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第6期22-22,共1页
Linear IgA bullous dermatosis (LABD) is a rare autoimmune vesiculobullous disorder characterized by variable clinical presentations that may mimic bullous pemphigoid, dermatitis herpetiformis, cicatricial pemphigoid a... Linear IgA bullous dermatosis (LABD) is a rare autoimmune vesiculobullous disorder characterized by variable clinical presentations that may mimic bullous pemphigoid, dermatitis herpetiformis, cicatricial pemphigoid and erythema multi- forme. A few cases of drug-induced LABD that clinically resembled toxic epidermal necrolysis (TEN) have been reported. A subset of patients with LABD have been found to be drug-induced: the most common drug being vancomycin. The diagnosisofLABDisconfirmedbythepresenceofalinearband of IgA along the basement membrane zone on direct immunofluorescence microscopy. We report a case of a 77- year-old man who presented to us with vancomycin-induced LABD that presented clinically as TEN, He had a complete recovery over a 3- week period following discontinuation of the vancomycin and the addition of oral dapsone therapy. It is important to be aware that drug-induced LABD can mimic TEN. 展开更多
关键词 IgA大疱病 大疱 多形性红斑 疱疹样皮炎 氨苯砜 直接免疫荧光法 瘢痕性 基膜 于中
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