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新型 TNF 治疗相关性结节病样肉芽肿病:一种被低估的并发症。

New onset sarcoid-like granulomatosis developing during anti-TNF therapy: an under-recognised complication.

机构信息

Department of Rheumatology, Westmead Hospital, Sydney, New South Wales, Australia.

出版信息

Intern Med J. 2012 Jan;42(1):89-94. doi: 10.1111/j.1445-5994.2011.02612.x.

DOI:10.1111/j.1445-5994.2011.02612.x
PMID:22389903
Abstract

Tumour necrosis factor-alpha (TNF-a) antagonists have advanced the treatment of inflammatory arthropathies, and are even considered for use in refractory sarcoidosis with some success. Paradoxically, cases of new onset sarcoidosis-like diseases are increasingly reported in patients receiving TNF-a antagonists. Here, we report three cases of sarcoid-like granulomatosis that developed during treatment with TNF-a antagonists. Review of the Biologics clinic data base at Westmead, Sydney, Australia identified three patients whom, during anti-TNF therapy, developed non-caseating granulomas consistent with sarcoidosis. These three cases are described with review of the literature from 2000 to 2009 using PubMed. One hundred and sixty-nine patients within our data base were reviewed for the period 2003–2009. Sarcoidosis-like granulomas developed in three patients within a period of 3 to 36 months of treatment with etanercept and/or adalimumab. All cases demonstrated non-infective, non-caseating granulomas on renal or lymph node biopsy. Improvement was seen in two cases upon cessation of TNF-a antagonist and steroid therapy. Interestingly, clinical deterioration was noted upon re-challenge with the same TNF-a antagonist in one patient. To date, a total of 37 cases of sarcoid-like granuloma development after anti-TNF therapy have been reported in the literature. Development of sarcoidosis-like granulomatosis in patients treated with TNF-a antagonists is a phenomenon previously under-recognised. All three anti-TNF agents have been observed to cause this phenomenon, suggesting a ‘class effect’ rather than being drug specific.

摘要

肿瘤坏死因子-α(TNF-a)拮抗剂在治疗炎症性关节炎方面取得了进展,甚至在一些难治性结节病中也取得了一定的成功。矛盾的是,在接受 TNF-a 拮抗剂治疗的患者中,越来越多的报告出现了新的结节病样疾病。在这里,我们报告了三例在 TNF-a 拮抗剂治疗期间发生的类结节病样肉芽肿病。对澳大利亚悉尼韦斯特米德的生物制剂临床数据的回顾发现了三例患者,在接受抗 TNF 治疗期间,出现了非干酪样肉芽肿,符合结节病。描述了这三个病例,并回顾了 2000 年至 2009 年期间使用 PubMed 的文献。在我们的数据库中,对 2003-2009 年期间的 169 例患者进行了回顾。在使用依那西普和/或阿达木单抗治疗的 3-36 个月期间,有三例患者出现了类结节病样肉芽肿。所有病例的肾或淋巴结活检均显示非感染性、非干酪样肉芽肿。两例患者在停止使用 TNF-a 拮抗剂和类固醇治疗后得到改善。有趣的是,在一名患者中,再次使用相同的 TNF-a 拮抗剂时,出现了临床恶化。迄今为止,文献中已报道了 37 例抗 TNF 治疗后出现类结节病样肉芽肿的病例。在接受 TNF-a 拮抗剂治疗的患者中出现类结节病样肉芽肿病是一种以前未被认识到的现象。所有三种抗 TNF 药物都被观察到引起这种现象,表明这是一种“类效应”,而不是药物特异性。

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