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Development of sarcoidosis 6-month post discontinuation of etanercept: coincidence or real association?

机译:停用依那西普后6个月结节病的发展:巧合还是真正的联系?

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There have been numerous reports of granulomatous diseases developing in patients receiving anti-tumour necrosis factor (TNF) therapy. Herein, we report a patient who developed sarcoidosis 6 months after discontinuation of etanercept. To date, all reported cases have occurred in patients undergoing ongoing treatment with TNF blockers with resolution on its discontinuation. A 47-year-old man was diagnosed with seropositive rheumatoid arthritis (RA) in 2003. He was initially treated with methotrexate and corticosteroids. In 2005, adalimumab was added due to ongoing disease activity. However, he had persistent low-grade synovitis of bilateral wrist joints and remained oral glucocorticoids dependent. In October 2008, adalimumab was switched to etanercept with marginal benefit; however, etanercept was continued until March 2009. Rituximab was discontinued due to an immediate allergic reaction. In September 2009, he developed bilateral ankle synovitis with erythema nodosum. Further investigations (chest X-ray and CT scan of thorax) revealed new development of bilateral hilar lymphadenopathy and interstitial nodular changes typical of sarcoidosis. His baseline therapy of methotrexate was continued. His recent repeat chest X-ray and CT scan of thorax (March 2010) has shown significant spontaneous resolution of his mediastinal lymphadenopathy and pulmonary nodules. Apart from the initial brief course of NSAIDs, his sarcoidosis resolved spontaneously without requiring any further therapy. For his rheumatoid arthritis, he has been recently commenced on abatacept and his baseline therapy of methotrexate has been continued. It remains speculative as to whether the concurrence of RA and sarcoidosis is purely serendipitous, or is related to an immunodysregulatory state attributable to TNF blockade.
机译:有许多报道称接受抗肿瘤坏死因子(TNF)治疗的患者出现肉芽肿性疾病。本文中,我们报告了停用依那西普6个月后出现结节病的患者。迄今为止,所有报道的病例都发生在接受TNF阻断剂持续治疗的患者中,并已终止治疗。一名47岁的男子在2003年被诊断出患有血清反应性类风湿关节炎(RA)。最初接受甲氨蝶呤和皮质类固醇治疗。 2005年,由于持续的疾病活动,添加了阿达木单抗。但是,他患有双侧腕关节持续性低度滑膜炎,并且仍然依赖口服糖皮质激素。 2008年10月,阿达木单抗转为依那西普,但获益不大。然而,依那西普一直持续到2009年3月。由于立即发生过敏反应,利妥昔单抗停药。 2009年9月,他患上了结节性红斑,发展为双侧踝关节滑膜炎。进一步的研究(胸部的X射线和CT扫描)揭示了双侧肺门淋巴结病的新发展和结节病典型的间质结节改变。他的甲氨蝶呤的基线治疗仍在继续。他最近对胸部进行了胸部X线检查和CT扫描(2010年3月),显示出他的纵隔淋巴结肿大和肺结节的明显自发消退。除了最初的短暂NSAID疗程外,他的结节病可自发消退,无需任何进一步的治疗。对于他的类风湿关节炎,他最近开始接受阿巴西普治疗,并继续进行甲氨蝶呤的基线治疗。关于RA和结节病的并发是否纯粹是偶然的,还是与可归因于TNF阻断的免疫调节状态有关,仍存在推测。

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