[免疫介导的坏死性肌病]。

Q3 Medicine Brain and Nerve Pub Date : 2024-05-01 DOI:10.11477/mf.1416202655
Akinori Uruha
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摘要

免疫介导的坏死性肌病(IMNM)是一种自身免疫性肌炎,其特点是肌肉中主要存在坏死和再生过程。抗-SRP和抗-HMGCR已被确定为IMNM特异性自身抗体。该病患者通常表现为重症肌无力和血清肌酸激酶(CK)水平明显升高。在某些病例中,与肌肉萎缩症的鉴别具有挑战性。当患者符合 "亚急性起病"、"高肌酸激酶血症超过 1000 IU/L "和 "临床诊断为肌营养不良,但缺乏分子诊断 "等条件时,应考虑到 IMNM 的可能性。建议测量自身抗体,包括抗-SRP 和 HMGCR 抗体。可使用皮质类固醇联合免疫抑制剂、静脉注射免疫球蛋白和利妥昔单抗进行治疗。
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[Immune-Mediated Necrotizing Myopathy].

Immune-mediated necrotizing myopathy (IMNM) is a form of autoimmune myositis characterized by the presence of necrotic and regenerating process as a major finding in the muscle. Anti-SRP and anti-HMGCR have been identified as IMNM-specific autoantibodies. Patients with this disease often present with severe muscle weakness and markedly elevated serum creatine kinase (CK) levels. Differentiation from muscular dystrophy is challenging in certain cases. When patients meet the condition "subacute onset", "hyperCKemia over 1000 IU/L", and "clinical diagnosis of muscular dystrophy lacking molecular diagnosis", the possibility of IMNM should be considered. Autoantibody measurement, including of anti-SRP and HMGCR antibodies, is recommended. Treatment with corticosteroid in combination with immunosuppressants, intravenous immunoglobulin, and rituximab can be performed.

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Brain and Nerve
Brain and Nerve Medicine-Neurology (clinical)
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