类风湿性关节炎患者英夫利昔单抗治疗后出现大疱性类天疱疮1例

Seongsoo Park, J. Lee
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引用次数: 1

摘要

大疱性类天疱疮是一种常见于老年人的自身免疫性表皮下起泡性疾病。它被称为自身免疫性大疱性皮肤病,估计患病率为4万分之一,没有性别或种族偏好。它具有自身免疫性质,免疫球蛋白(Ig) G和/或C3补体靶向位于表皮基底膜带的半粒酶体抗原。药物性类天疱疮虽然罕见,但可发生在服用青霉胺、呋塞米、卡托普利、青霉素或磺胺吡啶的患者中,但英夫利昔单抗引起的类天疱疮尚未报道。我们经历了一例因英夫利昔单抗引起的类天疱疮,54岁女性,有17年的类风湿关节炎病史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Bullous Pemphigoid Arising after Infliximab Therapy in a Patient with Rheumatoid Arthritis
Bullous pemphigoid is an autoimmune, subepidermal blistering disease commonly seen in the elderly. It is known as autoimmune bullous dermatoses with an estimated prevalence of 1 in 40,000 and shows no gender or racial predilection. It has an autoimmune nature with immunoglobulin (Ig) G and/or C3 complement targeting hemidesmosomal antigens located in the epidermal basement membrane zone. Drug-induced pemphigoid, although rare, can occur in patients taking penicillamine, furosemide, captopril, penicillin, or sulfasalazine, but infliximabinduced pemphigoid has not been reported. We experienced a case of infliximab-induced pemphigoid in 54-year-old woman with a 17-year history of rheumatoid arthritis.
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