Urbanits S, Grisold W, Zifko U, Budka H
Klinischen Institut für Neurologie, Universität Wien.
Wien Med Wochenschr. 1996;146(9-10):206-9.
Descriptions on patients with multifocal motor neuropathy with conduction block (MMNCB), including histology, nerve fiber teasing and electron microscopy on nerve biopsy, are rare. We report a 64-year old female patient with progredient weakness of the upper extremities without sensory deficit. Electrophysiology shows conduction blocks up to 80% in several examined motor nerves. A biopsy of the sensory sural nerve reveals features of a mixed axonal and de- and remyelinating neuropathy. Thus sural nerve biopsy contributes here significantly to differential diagnosis and supports an immune mediated pathogenesis of MMNCB.
关于伴有传导阻滞的多灶性运动神经病(MMNCB)患者的描述,包括组织学、神经活检的神经纤维分离及电子显微镜检查,较为罕见。我们报告一名64岁女性患者,上肢进行性无力且无感觉障碍。电生理学检查显示,在多条被检测的运动神经中传导阻滞高达80%。腓肠感觉神经活检显示为轴索性与脱髓鞘和再髓鞘性混合性神经病的特征。因此,腓肠神经活检在此处对鉴别诊断有显著贡献,并支持MMNCB的免疫介导发病机制。