Bady B, Brochier C
Rev Electroencephalogr Neurophysiol Clin. 1977 Apr-Jun;7(2):187-91. doi: 10.1016/s0370-4475(77)80078-6.
The authors report 4 cases of pseudo-myasthenic syndrome followed with EMG for a period varying from a few months to 4 years. They go over the electrophysiological points which led to the diagnosis: small amplitude of the muscle potential evoked by simple shock and, in particular, the phenomenon of potentiation which may reach 2000 p. 100 during repetitive stimulation at high frequencies. Study of the behaviour of the muscle potential during ischaemia, which was carried out twice, showed an absence of fatigue of the potential which may be considered a sign of disturbance at the muscle level of the motor-end plate. On the other hand, EMG signs of peripheral neuropathy, which were found 3 times, rather suggests a motor neuropathy responsible for the presynaptic block. In 3 patients guanidine had a beneficial effect and no signs of paraneoplastic aetiology had occurred yet. The fourth case, with a bronchial neoplasm discovered at autopsy, was clearly improved by injectable lidocaine, for which no explanation can be supplied.
作者报告了4例假重症肌无力综合征病例,对其进行了数月至4年不等的肌电图随访。他们回顾了做出诊断的电生理要点:单次电刺激诱发的肌肉电位幅度小,尤其是在高频重复刺激时可能达到2000%(100倍)的增强现象。两次进行的缺血期间肌肉电位行为研究表明,电位无疲劳现象,这可被视为运动终板肌肉水平存在紊乱的迹象。另一方面,3次发现的周围神经病变的肌电图征象,更提示是一种导致突触前阻滞的运动神经病。3例患者使用胍取得了有益效果,且尚未出现副肿瘤病因的迹象。第4例在尸检时发现有支气管肿瘤,注射利多卡因后明显好转,对此无法给出解释。