他克莫司诱导的耐药炎性肌病缓解:一个病例系列。

Karina Rotella, Milena Rodriguez Alvarez, Yair Saperstein, Manjeet S Bhamra, Su Zhaz Leon, Alekznder Feoktiztov, Isabel M McFarlane
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引用次数: 1

摘要

特发性炎症性肌病是一种罕见的自身免疫性疾病,其特征是近端肌肉无力,肌肉酶升高,肌电图异常和影像学检查显示水肿和炎症区域。炎性肌病的初始治疗方法包括类固醇和免疫抑制剂,大多数个体对治疗反应满意。然而,治疗难治性肌病促使临床医生使用二线药物来达到缓解。在这个病例系列中,我们描述了3例难治性特发性炎性肌病患者,他们接受了他克莫司(TAC)加霉酚酸酯(MMF)和类固醇治疗,获得了临床和生化缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tacrolimus-Induced Remission in Drug Resistant Inflammatory Myopathy: A Case Series.

Idiopathic inflammatory myopathies are rare autoimmune disorders characterized by proximal muscle weakness, elevation of muscle enzymes, abnormal electromyogram and imaging studies revealing areas of edema and inflammation. Initial approach to inflammatory myopathies includes steroids and immunosuppressive agents, with most individuals responding satisfactorily to therapy. However, treatment-refractory myopathies prompts clinicians to use second line agents to achieve remission. In this case series, we describe three patients with refractory idiopathic inflammatory myopathies who were treated with tacrolimus (TAC) added to mycophenolate mofetil (MMF) and steroid therapy, who achieved clinical and biochemical remission.

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