Oh S J
Department of Neurology, University of Alabama, Birmingham.
Muscle Nerve. 1989 May;12(5):371-7. doi: 10.1002/mus.880120506.
Various parameters of single- fiber electromyography (SFEMG) were studied in 19 patients with electrophysiologically and histologically proven chronic demyelinating neuropathy. The mean duration of disease at the time of testing was four years. Motor nerve conduction in the median nerve was abnormal in all patients, whereas sensory nerve conduction was abnormal in all but one. Needle EMG in the extensor digitorum communis (EDC) muscle showed rare fibrillations and fasciculations and some abnormal motor unit potentials in most of patients. SFEMG in the EDC muscle showed an increased fiber density in seven cases (37%) and minimally abnormal jitter in 14 cases (74%). Single-fiber action potentials were stable, whereas blocking was rare. Fiber density was significantly increased in patients with fibrillation in the conventional needle EMG. Our study showed that the SFEMG is mildly abnormal in many patients with demyelinating neuropathy and that this test is useful in detecting and quantitating axonal degeneration in demyelinating neuropathy.
对19例经电生理和组织学证实为慢性脱髓鞘性神经病的患者进行了单纤维肌电图(SFEMG)的各项参数研究。测试时疾病的平均病程为4年。所有患者正中神经运动神经传导均异常,而除1例患者外所有患者感觉神经传导均异常。指总伸肌(EDC)肌肉的针极肌电图显示,大多数患者有罕见的纤颤和束颤以及一些异常运动单位电位。EDC肌肉的SFEMG显示7例(37%)纤维密度增加,14例(74%)有轻度异常的颤抖。单纤维动作电位稳定,阻滞罕见。传统针极肌电图有纤颤的患者纤维密度显著增加。我们的研究表明,许多脱髓鞘性神经病患者的SFEMG有轻度异常,且该检查有助于检测和定量脱髓鞘性神经病中的轴索变性。