他汀类药物诱导的坏死性自身免疫性肌病的诊断和治疗

A. B. Sumarokov, M. Ezhov
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引用次数: 0

摘要

他汀类药物诱导的坏死性自身免疫性肌病(SINAM)是他汀类药物治疗的罕见并发症。SINAM属于特发性炎症性肌病,其特征是肌肉细胞坏死和再生导致肌肉萎缩。肌肉组织中没有明显的淋巴细胞浸润。上肢和下肢进行性肌无力是SINAM的主要临床表现。自身免疫机制的发病机制解释了他汀类药物停药治疗效果的缺失和复发的风险。SINAM的诊断可以通过临床和血清学资料、肌肉活检和无创方法(MRI、超声)的结果来确定。早期开始免疫抑制治疗对于实现siam的治愈至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnosis and treatment of statin-induced necrotizing autoimmune myopathy
Statin-induced necrotizing autoimmune myopathy (SINAM) is an exceptionally rare complication of statin therapy. SINAM belongs to the group of idiopathic inflammatory myopathies and is characterized by muscle cell necrosis and regeneration leading to muscle atrophy. Prominent lymphocytic infiltrates in muscle tissue are absent. Progressive muscle weakness in upper and lower extremities is the main clinical manifestation of SINAM. Autoimmune mechanism of pathogenesis explain the absense of therapeutic effect of statin discontinuation and the risk of relapses. Diagnosis of SINAM can be established by clinical and serologic data, muscle biopsy and the results on noninvasive methods (MRI, ultrasound). Early initiation of immunosuppressive treatment is essential to achieve the cure of SINAM.
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