Cowan J M, Rothwell J C, Wise R J, Marsden C D
J Neurol Neurosurg Psychiatry. 1986 Jul;49(7):796-807. doi: 10.1136/jnnp.49.7.796.
A patient is described who had a combination of stimulus-sensitive cortical myoclonus, epilepsia partialis continua, and Jacksonian motor epilepsy. He eventually required surgery because of the severity of his seizures. Electrophysiological recordings made before and during surgery, and PET scans performed before surgery identified an abnormal area of cerebral cortex in the postcentral parietal region. It is suggested that the stimulus-sensitive myoclonus arose because input into this region from peripheral sensory afferents produced an abnormal discharge which was fed forwards via cortico-cortical connections to the precentral motor cortex, to produce a reflex muscle jerk. The epilepsia partialis continua may have been caused by spontaneous discharges arising in the same region of parietal cortex. Both forms of jerking disappeared after resection of this part of the cortex.
本文描述了一名患有刺激敏感性皮质肌阵挛、持续性部分性癫痫和杰克逊运动性癫痫的患者。由于癫痫发作严重,他最终需要接受手术。手术前后进行的电生理记录以及术前进行的PET扫描确定了中央后顶叶区域的大脑皮质存在异常区域。有人认为,刺激敏感性肌阵挛的出现是因为外周感觉传入神经向该区域的输入产生了异常放电,该放电通过皮质-皮质连接向前传导至中央前运动皮层,从而产生反射性肌肉抽搐。持续性部分性癫痫可能是由顶叶皮质同一区域的自发放电引起的。切除该部分皮质后,两种抽搐形式均消失。