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卡恩斯-塞尔综合征的肌病理学进展:一项形态学随访研究。

Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.

作者信息

Reichmann H, Gold R, Meurers B, Naumann M, Seibel P, Walter U, Klopstock T

机构信息

Department of Neurology, University of Würzburg, Germany.

出版信息

Acta Neuropathol. 1993;85(6):679-81. doi: 10.1007/BF00334681.

Abstract

We report on the progression of myopathology by comparing two biopsies from a patient with a Kearns-Sayre-Syndrome. The first biopsy was taken in 1979 and showed 10% ragged-red fibers. Myopathic changes were slight including internal nuclei and fiber splitting in 10% of the fibers. Electron microscopy revealed typical mitochondrial abnormalities with regard to number and shape. In 1989 a second biopsy was performed for an extended analysis of mitochondrial DNA. This time less than 5% of all fibers were ragged-red. Severe myopathic changes could be detected which so far has rarely been reported in mitochondrial cytopathy.

摘要

我们通过比较一名患有卡恩斯-塞尔综合征患者的两次活检结果来报告肌病的进展情况。第一次活检于1979年进行,显示有10%的破碎红纤维。肌病性改变轻微,包括10%的纤维出现内部细胞核和纤维分裂。电子显微镜检查显示线粒体在数量和形状方面存在典型异常。1989年进行了第二次活检,以对线粒体DNA进行进一步分析。这次,所有纤维中破碎红纤维不到5%。可以检测到严重的肌病性改变,这在线粒体细胞病中迄今为止很少有报道。

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