Immune-mediated necrotizing myopathy: Report of two cases

被引：0

作者：

Bi-Hong Chen ^{[1
]}

Xue-Min Zhu ^{[2
]}

Lei Xie ^{[2
]}

Huai-Qiang Hu ^{[3
]}

机构：

[1] Department of Clinical Medicine,Weifang Medical University

[2] School of Clinical Medicine,Weifang Medical University

[3] Department of Neurology,The 960th Hospital of People′s Liberation Army

来源：

World Journal of Clinical Cases | 2023年 / 15期

关键词：

D O I：

暂无

中图分类号：

R593.2 [自身免疫性疾病、结缔组织疾病];

学科分类号：

1002 ; 100201 ;

摘要：

BACKGROUND Immune-mediated necrotizing myopathy is a rare autoimmune myopathy characterized by muscle weakness and elevated serum creatine kinase, with unique skeletal muscle pathology and magnetic resonance imaging features.CASE SUMMARY In this paper, two patients are reported: One was positive for anti-signal recognition particle antibody, and the other was positive for anti-3-hydroxy-3-methylglutaryl coenzyme A reductase antibody.CONCLUSION The clinical characteristics and treatment of the two patients were analysed, and the literature was reviewed to improve the recognition, diagnosis, and treatment of this disease.

引用

页码：3552 / 3559

页数：8

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