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依那西普诱导的皮肤和肺部结节病样肉芽肿在使用阿达木单抗后消退。

Etanercept-induced cutaneous and pulmonary sarcoid-like granulomas resolving with adalimumab.

作者信息

Burns Ariel M, Green Peter J, Pasternak Sylvia

机构信息

Department of Medicine, Division of Dermatology, Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Cutan Pathol. 2012 Feb;39(2):289-93. doi: 10.1111/j.1600-0560.2011.01795.x. Epub 2011 Sep 7.

DOI:10.1111/j.1600-0560.2011.01795.x
PMID:21899592
Abstract

A 59-year-old female with rheumatoid arthritis on etanercept therapy presented with a 7-cm-large subcutaneous forearm mass. Multiple smaller nodules subsequently developed on the upper and lower extremities. Except for a new cough, the patient was systemically well. Biopsy of the mass showed sarcoidal type granulomatous inflammation with nodular aggregations of non-necrotizing epithelioid histiocytes in the subcutis. A chest computed tomography (CT) scan showed mediastinal adenopathy consistent with pulmonary sarcoidosis. Etanercept was discontinued, and the patient was started on adalimumab for rheumatoid arthritis control. The cutaneous nodules fully resolved in 6 months with no additional treatment. A 4-month follow-up CT scan showed significant regression of mediastinal adenopathy. The patient has since been maintained on adalimumab therapy for 2 years with no recurrence of sarcoid-like manifestations. Biologic response modifiers targeting tumor necrosis factor alpha (TNFα) are effective treatments of chronic inflammatory conditions such as rheumatoid arthritis and psoriasis. TNFα represents a major cytokine in granuloma formation, and TNFα inhibitors are sometimes efficacious in the treatment of sarcoidosis. Paradoxically, there is a small volume of literature implicating TNFα inhibitors in the development of sarcoid-like disease. We present this case to promote the recognition of TNFα inhibitor-induced sarcoidosis and to illustrate the wide clinicopathologic differential of sarcoidal type granulomas.

摘要

一名59岁患有类风湿关节炎且正在接受依那西普治疗的女性,出现了一个7厘米大的前臂皮下肿物。随后,其上下肢又出现了多个较小的结节。除了新发咳嗽外,患者全身状况良好。肿物活检显示为结节病样肉芽肿性炎症,皮下有非坏死性上皮样组织细胞的结节状聚集。胸部计算机断层扫描(CT)显示纵隔淋巴结肿大,符合肺结节病表现。停用依那西普,开始使用阿达木单抗控制类风湿关节炎。未进行额外治疗,皮肤结节在6个月内完全消退。4个月后的随访CT扫描显示纵隔淋巴结肿大明显消退。此后,患者接受阿达木单抗治疗2年,未再出现结节病样表现。靶向肿瘤坏死因子α(TNFα)的生物反应调节剂是类风湿关节炎和银屑病等慢性炎症性疾病的有效治疗方法。TNFα是肉芽肿形成中的一种主要细胞因子,TNFα抑制剂有时对结节病有效。矛盾的是,有少量文献提示TNFα抑制剂与结节病样疾病的发生有关。我们报告此病例以提高对TNFα抑制剂诱发结节病的认识,并说明结节病样肉芽肿广泛的临床病理鉴别诊断。

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