Otani K, Imai K, Futagi Y, Yanagihara K
Department of Pediatric Neurology, Osaka Medical Center, Japan.
Dev Med Child Neurol. 1995 Oct;37(10):933-6. doi: 10.1111/j.1469-8749.1995.tb11945.x.
Secondary sensory seizures (SSS) are very rare epileptic seizures. A 14-year-old male patient with habitual painful seizures of the backs of both hands since the age of four is reported. The painful seizures were rarely followed by impairment of consciousness. Ictal EEG showed 4 to 6Hz rhythmic waves over the right anterior and mid-temporal area following complaints of pain. The absence of tumorous lesions on brain CT or MRI, childhood onset and the absence of combined seizures were characteristic features of this case compared with other patients reported to have SSS.
继发性感觉性癫痫发作（SSS）是非常罕见的癫痫发作类型。本文报道了一名14岁男性患者，自4岁起双手背部习惯性疼痛发作。疼痛发作很少伴有意识障碍。发作期脑电图显示，在主诉疼痛后，右侧前颞叶和颞中区出现4至6Hz的节律性波。与其他报道的继发性感觉性癫痫发作患者相比，该病例的特征为脑CT或MRI未发现肿瘤性病变、儿童期起病且无合并发作。
