Schulze-Bonhage A, Knott H, Ferbert A
Neurologische Klinik, Städtische Kliniken Kassel, Germany.
Mov Disord. 1996 Jan;11(1):87-90. doi: 10.1002/mds.870110116.
The clinical and electrophysiological features of stimulus-sensitive truncal myoclonus are described in a 49-year-old woman. Touching the skin of the back and abdomen would evoke jerks in both ipsilateral and contralateral axial muscles; there was no spontaneous jerking. Multichannel EMG recordings showed bilateral short-latency muscle bursts at truncal recording sites both rostral and caudal to stimulus sites. The short latencies of muscle bursts in adjacent segments give evidence of a spinal origin of myoclonus; the pattern of recruitment and the velocity of spread suggest the involvement of propriospinal pathways. The presence of intrathecal IgG synthesis and of oligoclonal bands in the CSF point towards an inflammatory process which may underly the unusual type of myoclonus in this patient.
本文描述了一名49岁女性刺激敏感性躯干肌阵挛的临床和电生理特征。触摸背部和腹部皮肤会诱发同侧和对侧轴向肌肉的抽搐;无自发抽搐。多通道肌电图记录显示,在刺激部位头侧和尾侧的躯干记录部位均出现双侧短潜伏期肌肉爆发。相邻节段肌肉爆发的短潜伏期证明肌阵挛起源于脊髓;募集模式和传播速度提示脊髓固有通路受累。脑脊液中鞘内IgG合成及寡克隆带的存在表明存在炎症过程,这可能是该患者不寻常类型肌阵挛的基础。