阿巴接受和他克莫司治疗难治性免疫介导的坏死性肌病:一项基于病例的回顾

Camargo Macias Kathlyn, B. Karan, Chawla Ambreesh Bhanusali Neha
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引用次数: 0

摘要

特发性炎性肌病的特征是肌肉无力、血清肌酶水平升高、肌电图异常、肌炎特异性自身抗体(msa)的存在以及肌肉活检结果的炎症。免疫介导的坏死性肌病(IMNM)是IIM的一个子集,通常对标准的免疫抑制治疗有耐药性,需要多种治疗药物的组合。我们报告一例中年男性抗信号识别粒子(SRP) IMNM阳性,在标准护理治疗失败后对阿巴接受和他克莫司有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of refractory immune-mediated necrotizing myopathy with abatacept and tacrolimus: A case-based review
Idiopathic inflammatory myopathies are characterized by muscle weakness, elevation in serum muscle enzyme levels, electromyography abnormalities, presence of Myositis Specific Autoantibodies (MSAs) and findings of inflammation on muscle biopsy. Immune-mediated necrotizing myopathy (IMNM) is a subset of IIM that is often resistant to standard immunosuppressive therapy, requiring multiple combinations of therapeutic agents. We present a case of a middle-aged man with positive anti-Signal Recognition Particle (SRP) IMNM who responded to abatacept and tacrolimus after failing standard of care treatment.
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