Beyenburg S, von Wersebe O, Zierz S
Neurologische Universitätsklinik, Bonn.
Nervenarzt. 1991 Aug;62(8):506-11.
We describe a 53-year-old patient with a progressive mitochondrial myopathy of late-onset, restricted to skeletal muscle only without external ophthalmoplegia. The myopathy developed at the age of 46 years initially with exercise intolerance and subsequently progressive permanent muscle weakness. Muscle biopsy revealed severe myopathic changes, ragged red fibers, and a marked multifocal cytochrome-c-oxidase deficiency. Biochemical analysis showed a deficiency of complexes I and IV of the mitochondrial respiratory chain. Genetic analysis of mitochondrial DNA revealed no deletions. Mitochondrial myopathies restricted to skeletal muscle have to be considered in the differential diagnosis of late-onset progressive myopathies.
我们描述了一名53岁的患者,患有迟发性进行性线粒体肌病,仅累及骨骼肌,无眼外肌麻痹。该肌病于46岁时发病,最初表现为运动不耐受,随后逐渐发展为永久性肌肉无力。肌肉活检显示严重的肌病改变、破碎红纤维和明显的多灶性细胞色素c氧化酶缺乏。生化分析显示线粒体呼吸链复合体I和IV缺乏。线粒体DNA基因分析未发现缺失。在迟发性进行性肌病的鉴别诊断中,必须考虑仅累及骨骼肌的线粒体肌病。