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系统性结节病表现为慢性丙型肝炎干扰素-α治疗继发的肉芽肿性纹身反应并文献复习

Systemic sarcoidosis presenting as a granulomatous tattoo reaction secondary to interferon-alpha treatment for chronic hepatitis C and review of the literature.

作者信息

Nawras Ali, Alsolaiman Mohammad M, Mehboob Shahid, Bartholomew Catherine, Maliakkal Benedict

机构信息

Department of Gastroenterology, Albany Medical College, New York 12208, USA.

出版信息

Dig Dis Sci. 2002 Jul;47(7):1627-31. doi: 10.1023/a:1015843908536.

Abstract

Sarcoidosis is a multisystem granulomatous disease of unknown etiology. Immune alterations involving heightened T-helper-1 responses have been proposed to play a major role in the pathogenesis of sarcoidosis. Interferon-alpha therapy and hepatitis C infection have been implicated in the development of a variety of autoimmune diseases. However, despite the wide use of IFN-alpha therapy for hepatitis C, only a few cases of sarcoidosis have been reported in this context. We report the case of a 42-year-old white female with hepatitis C, who developed systemic sarcoidosis shortly after therapy with IFN-alpha2b. The disease was heralded by the appearance of a cutaneous sarcoid/ foreign body granulomatous reaction at the site of an old tattoo. The sarcoidosis responded to a short course of oral prednisone therapy. We also reviewed the other reported cases and discussed the possible immunological mechanisms involved.

摘要

结节病是一种病因不明的多系统肉芽肿性疾病。有观点认为,涉及辅助性T细胞1型反应增强的免疫改变在结节病的发病机制中起主要作用。α干扰素治疗和丙型肝炎感染与多种自身免疫性疾病的发生有关。然而,尽管α干扰素疗法广泛用于治疗丙型肝炎,但在此背景下仅报告了少数结节病病例。我们报告了一例42岁的丙型肝炎白人女性病例,该患者在接受α干扰素2b治疗后不久就出现了系统性结节病。该病以旧纹身部位出现皮肤结节病/异物肉芽肿反应为先兆。该结节病对短期口服泼尼松治疗有反应。我们还回顾了其他报告的病例,并讨论了可能涉及的免疫机制。

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