Umeoka Shuichi, Baba Koichi, Terada Kiyohito, Matsuda Kazumi, Tottori Takayasu, Usui Naotaka, Usui Keiko, Nakamura Fumihiro, Inoue Yushi, Fujiwara Tateki, Mihara Tadahiro
Department of Neurological Surgery, National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan.
Epileptic Disord. 2007 Dec;9(4):443-8. doi: 10.1684/epd.2007.0131.
We report a patient manifesting seizures with bilateral symmetric tonic posturing, which were markedly reduced after resection of the left precuneus. A 16-year-old man had sudden onset, complex partial seizures with bilateral symmetric tonic posturing since the age of eight years. Magnetic resonance fluid-attenuated inversion-recovery imaging revealed a hyperintense lesion in left precuneus. In almost all focal seizures recorded during an invasive EEG evaluation, ictal onset was detected from the inferomesial aspect of the lesion, but fast paroxysmal discharges from the ipsilateral supplementary motor area (SMA) were observed just before the clinical onset. After surgical excision of the EEG onset zone, including the lesion, seizure frequency was markedly (> 95%) reduced. By the 20th month after surgery, there were only brief nocturnal seizures involving slight elevation of both shoulders and slight abduction of both arms, with preservation of consciousness occurring once every few days. Invasive EEG findings and surgical outcome suggested that the epileptic activity originating from the epileptogenic zone may have propagated to the symptomatogenic zone including mainly the ipsilateral SMA. In summary, we report an interesting case of bilateral symmetric tonic posturing suggesting propagation to the SMA. MRI and invasive EEG confirmed the epileptogenic focus as a precuneate cortical dysplasia lesion.[Published with video sequences].
我们报告了一名表现为双侧对称强直性姿势发作的患者,在切除左侧楔前叶后发作明显减少。一名16岁男性自8岁起突然发病,出现伴有双侧对称强直性姿势的复杂部分性发作。磁共振液体衰减反转恢复成像显示左侧楔前叶有一个高信号病变。在侵入性脑电图评估记录的几乎所有局灶性发作中,发作起始于病变的内下侧,但在临床发作前观察到同侧辅助运动区(SMA)的快速阵发性放电。在手术切除包括病变在内的脑电图发作起始区后,发作频率显著降低(>95%)。术后第20个月,仅出现短暂的夜间发作,表现为双肩轻度抬高和双臂轻度外展,每隔几天出现一次意识保留。侵入性脑电图结果和手术结果表明,起源于致痫区的癫痫活动可能已经传播到主要包括同侧SMA的症状发生区。总之,我们报告了一例有趣的双侧对称强直性姿势发作病例,提示其传播至SMA。MRI和侵入性脑电图证实致痫灶为楔前叶皮质发育异常病变。[附视频序列发表]