One case of toxic epidermal necrolysis after treatment with belimumab in a patient with systemic lupus erythematosus

Q4 Medicine
M. Dună, D. Balanescu, C. Iosif, N. Copcă, D. Predețeanu, R. Ionescu
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引用次数: 0

Abstract

Belimumab is a human immunoglobulin G1-lambda-1 (IgG1-λ) monoclonal antibody that targets the soluble BLyS human protein, also known as B-cell activating factor (BAFF) approved for the treatment of systemic lupus erythematosus (SLE). Serious and sometimes fatal infections have been reported in patients receiving novel immunosuppressive agents, including belimumab. Thus, physicians should exercise caution when considering belimumab in patients with SLE. A 50-year-old woman with SLE presented with a severe, diffuse rash two months after initiating treatment with belimumab. A skin biopsy revealed epidermal necrolysis with keratinocyte detachment and apoptosis in the basal layer of the epidermis, suggestive for toxic epidermal necrolysis (TEN). Belimumab was discontinued and 500 mg of pulse IV methylprednisolone therapy every day for 3 days were administered, with resolution of the skin lesions in the following days. To the best of our knowledge, this is the first case of belimumab-associated TEN.
贝利木单抗治疗系统性红斑狼疮后中毒性表皮坏死松解1例
Belimumab是一种人免疫球蛋白G1-lambda-1(IgG1-λ)单克隆抗体,靶向可溶性BLyS人蛋白,也称为B细胞活化因子(BAFF),被批准用于治疗系统性红斑狼疮(SLE)。据报道,接受新型免疫抑制剂(包括贝利单抗)治疗的患者出现严重甚至致命的感染。因此,在系统性红斑狼疮患者中使用贝利单抗时,医生应谨慎。一名50岁的SLE妇女在开始使用贝利单抗治疗两个月后出现严重的弥漫性皮疹。皮肤活检显示表皮坏死松解,表皮基底层角质形成细胞脱落和凋亡,提示毒性表皮坏死松脱(TEN)。停用Belimumab,每天给予500 mg甲基强的松龙脉冲IV治疗,持续3天,随后几天皮肤损伤得到缓解。据我们所知,这是第一例belimumab相关TEN病例。
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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CiteScore
0.10
自引率
0.00%
发文量
22
审稿时长
4 weeks
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