Yiannikas C, McLeod J G, Pollard J D, Baverstock J
Ann Neurol. 1986 Aug;20(2):249-57. doi: 10.1002/ana.410200211.
Twenty patients with mitochondrial myopathy were investigated for the presence of peripheral neuropathy. There were clinical features of a mild sensorimotor neuropathy in 5 patients (25%) and nerve conduction studies were abnormal in 10 patients (50%). Electrophysiological studies of the whole group showed significant impairment of motor and sensory conduction, compared with controls. Sural nerve biopsy and morphometric studies were performed on 4 patients with clinical neuropathy. There was a reduction in density of myelinated fibers and electron microscope features of axonal degeneration affecting myelinated and unmyelinated fibers. Abnormal mitochondria containing paracrystalline inclusions were seen in the Schwann cell cytoplasm of two nerves.
对20例线粒体肌病患者进行了周围神经病变检查。5例患者(25%)有轻度感觉运动神经病变的临床特征,10例患者(50%)神经传导研究异常。与对照组相比,全组的电生理研究显示运动和感觉传导有明显损害。对4例有临床神经病变的患者进行了腓肠神经活检和形态计量学研究。有髓纤维密度降低,轴突退变的电镜特征影响有髓和无髓纤维。在两条神经的施万细胞胞质中可见含有副结晶包涵体的异常线粒体。