治疗史蒂文斯-约翰逊综合征/毒性表皮坏死症的联合疗法:病例系列和文献综述

Soumi Biswas, Arun Achar, Chinmay Bera, Adityendu Chakraborty, Mahasweta Ghosh, Monika Kumari
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引用次数: 0

摘要

史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死(TEN)是一种危及生命的皮肤和粘膜疾病,主要由药物引起。许多研究侧重于改变免疫反应的治疗,如皮质类固醇、IVIG、环孢素、生物制剂,如 TNF-α 抑制剂 etanercept、英夫利昔单抗等。但同时使用两种免疫调节药物的研究很少。然而,目前还没有针对 SJS/TEN 患者的标准化治疗方案。我们介绍了同时使用全身皮质类固醇和环孢素治疗 10 例 SJS-TEN 患者的病例系列。我们回顾了有关单独使用全身性皮质类固醇、环孢素以及同时使用这两种药物治疗 SJS/TEN 的文献,包括各种结果测量--病情稳定、死亡率、住院时间以及与其他全身性药物的比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination therapy in the treatment of Stevens-Johnson syndrome/toxic epidermal necrolysis: a case series and review of literature
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are life-threatening disease of skin and mucous membrane that are mostly caused by drugs. Many studies have focussed on treatment that modify immunologic responses like corticosteroid, IVIG, cyclosporine, biologics like TNF-α inhibitors etanercept, infliximab etc. But there are few studies available on using two immunomodifier drugs simultaneously. However, no standardized treatment protocol has been established for SJS/TEN patients. We present a case-series of 10 SJS-TEN patients treated with both systemic corticosteroid and cyclosporine. We provide a review of literature on individual systemic corticosteroid, cyclosporine and also simultaneous use of both agents for SJS/TEN, including various outcome measures-stabilization, mortality rate, hospital length of stay and comparison to other systemic agents.
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