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肌炎的模仿疾病

Myositis Mimics.

作者信息

Michelle E Harlan, Mammen Andrew L

机构信息

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Curr Rheumatol Rep. 2015 Oct;17(10):63. doi: 10.1007/s11926-015-0541-0.

Abstract

Patients with autoimmune myositis typically present with muscle weakness, elevated serum levels of muscle enzymes, and abnormal muscle biopsies. However, patients with other acquired myopathies or genetic muscle diseases may have remarkably similar presentations. Making the correct diagnosis of another muscle disease can prevent these patients from being exposed to the risks of immunosuppressive medications, which benefit those with myositis, but not those with other types of muscle disease. Here, we review some of the most common acquired and inherited muscle diseases that can mimic autoimmune myositis, including inclusion body myositis, limb girdle muscular dystrophies, metabolic myopathies, mitochondrial myopathies, and endocrine myopathies. We emphasize aspects of the medical history, physical exam, laboratory evaluation, and muscle biopsy analysis that can help clinicians distinguish myositis mimics from true autoimmune myositis.

摘要

自身免疫性肌炎患者通常表现为肌肉无力、血清肌肉酶水平升高以及肌肉活检异常。然而,患有其他获得性肌病或遗传性肌肉疾病的患者可能有非常相似的表现。正确诊断出另一种肌肉疾病可以避免这些患者面临免疫抑制药物的风险,免疫抑制药物对肌炎患者有益,但对其他类型的肌肉疾病患者则不然。在此,我们回顾一些最常见的可模仿自身免疫性肌炎的获得性和遗传性肌肉疾病,包括包涵体肌炎、肢带型肌营养不良症、代谢性肌病、线粒体肌病和内分泌性肌病。我们强调病史、体格检查、实验室评估和肌肉活检分析等方面,这些有助于临床医生区分模仿肌炎的疾病与真正的自身免疫性肌炎。

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