他汀类药物继发的严重抗hmg - coar坏死性自身免疫性肌病

Case Reports in Rheumatology Pub Date : 2022-09-16 eCollection Date: 2022-01-01 DOI:10.1155/2022/6120424
Priyanjali Pulipati, Jayakar Kamantha Reddy, Syed Ali Husain
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引用次数: 1

摘要

免疫介导的坏死性肌病是一种罕见但使人衰弱的疾病,可由药物、毒素或癌症引发。它在表现上与多发性肌炎相似,但可通过肌肉活检来鉴别。我们提出一个病例79岁的男性他汀类药物治疗谁提出了近端肌无力和肌酐激酶(CK)水平升高。他接受了免疫介导的坏死性肌病的确证性肌肉活检。不幸的是,尽管及时诊断和治疗,患者的病情最终升级,涉及呼吸和食管肌肉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe Anti-HMG-CoAR Necrotizing Autoimmune Myopathy Secondary to Statin Use.

Immune-mediated necrotizing myopathy is an uncommon but debilitating disease that can be triggered by drugs, toxins, or cancer. It is similar to polymyositis in presentation but is differentiated by findings on muscle biopsy. We present a case of a 79-year-old male on statin therapy who presented with proximal muscle weakness and elevated creatinine kinase (CK) levels. He had a confirmatory muscle biopsy for immune-mediated necrotizing myopathy. Unfortunately, the patient's condition eventually escalated, involving respiratory and esophageal muscles in spite of prompt diagnosis and treatment.

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