Peculiar histological and ultrastructural skeletal muscle alterations in a patient with CMV infection and autoimmune myositis: case evaluation and brief literature review.

M. Ripolone, L. Napoli, V. Mantero, M. Sciacco, S. Zanotti
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引用次数: 2

Abstract

We report the case of a young woman with CMV infection, high level of creatine kinase and myopathy. Electromyography showed a myopathic pattern. Muscle biopsy showed a marked increase of NADH enzymatic activity in the central area of almost all type I fibres, few degenerative and necrotic fibres and scattered mononuclear cell infiltrates. Ultrastructural analysis showed a marked disarrangement of sarcomeric structure and large inclusions of thin filaments in some fibres, while immunohistochemistry evidenced alteration in desmin, actin and αB-crystallin protein signals. PCR for CMV detection on muscle sections was negative. Histological, immunological and ultrastructural evaluations were compatible with a necrotic inflammatory myopathy. The correlations between CMV liver infection and the myopathic pattern are discussed. This case underscores the need to consider CMV infection in the differential diagnosis of myopathy with undetermined aetiology, quickly providing directions for a targeted muscle pharmacological intervention.
巨细胞病毒感染和自身免疫性肌炎患者的特殊组织学和超微结构骨骼肌改变:病例评估和简要文献回顾。
我们报告的情况下,年轻妇女巨细胞病毒感染,高水平的肌酸激酶和肌病。肌电图显示肌病型。肌肉活检显示几乎所有I型纤维的中心区域NADH酶活性明显增加,少数退行性和坏死纤维和分散的单核细胞浸润。超微结构分析显示肌肉组织结构明显紊乱,部分纤维中有大量细丝包涵,免疫组化显示desmin、actin和α b -晶体蛋白信号改变。肌肉切片CMV PCR检测结果为阴性。组织学、免疫学和超微结构评价与坏死性炎症性肌病一致。讨论了巨细胞病毒肝脏感染与肌病类型的相关性。该病例强调了在病因不明的肌病鉴别诊断中考虑巨细胞病毒感染的必要性,为有针对性的肌肉药物干预提供了快速指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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