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成人起病型线粒体肌病

Adult-onset mitochondrial myopathy.

作者信息

Fernandez-Sola J, Casademont J, Grau J M, Graus F, Cardellach F, Pedrol E, Urbano-Marquez A

机构信息

Internal Medicine Service, Hospital Clínic, Barcelona, Spain.

出版信息

Postgrad Med J. 1992 Mar;68(797):212-5. doi: 10.1136/pgmj.68.797.212.

Abstract

Mitochondrial diseases are polymorphic entities which may affect many organs and systems. Skeletal muscle involvement is frequent in the context of systemic mitochondrial disease, but adult-onset pure mitochondrial myopathy appears to be rare. We report 3 patients with progressive skeletal mitochondrial myopathy starting in adult age. In all cases, the proximal myopathy was the only clinical feature. Mitochondrial pathology was confirmed by evidence of ragged-red fibres in muscle histochemistry, an abnormal mitochondrial morphology in electron microscopy and by exclusion of other underlying diseases. No deletions of mitochondrial DNA were found. We emphasize the need to look for a mitochondrial disorder in some non-specific myopathies starting in adult life.

摘要

线粒体疾病是多形性疾病,可累及多个器官和系统。在全身性线粒体疾病中,骨骼肌受累很常见,但成人起病的单纯线粒体肌病似乎很少见。我们报告了3例成年起病的进行性骨骼肌线粒体肌病患者。所有病例中,近端肌病是唯一的临床特征。肌肉组织化学检查发现破碎红纤维、电子显微镜下线粒体形态异常以及排除其他潜在疾病,均证实了线粒体病理改变。未发现线粒体DNA缺失。我们强调,对于一些成年起病的非特异性肌病,有必要排查线粒体疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbb/2399258/a1b24921a8d9/postmedj00063-0058-a.jpg

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