Olson D M, Chugani H T, Shewmon D A, Phelps M E, Peacock W J
Department of Neurology, UCLA School of Medicine 90024.
Epilepsia. 1990 Nov-Dec;31(6):731-9. doi: 10.1111/j.1528-1157.1990.tb05514.x.
The relationship between focal disturbances of glucose utilization demonstrated by positron emission tomography (PET) and electrophysiologic abnormalities defined by intraoperative electrocorticography (ECoG) was studied in eight children (aged 13 months to 12 years) who underwent cortical resection because of intractable seizures. None of the children had pure temporal lobe epilepsy. Computed tomography (CT) and/or magnetic resonance imaging (MRI) were normal in four of the eight children. The scalp electroencephalogram (EEG) showed lateralized interictal epileptiform abnormalities in all eight and lateralized ictal onset in five of eight. In seven children, interictal PET showed focal hypometabolism; the eighth child had focal, ictal hypermetabolism. ECoG at the time of surgery showed epileptiform spiking, slowing, and/or suppression of normal background activity that in every case corresponded to the focus on PET scan. The ECoG findings support the notion that in children with epilepsy focal metabolic abnormalities on PET correspond to electrophysiologically abnormal areas of cortex, which are presumably also the epileptogenic regions. Such areas can appear normal on anatomic imaging studies (CT and MRI). When ictal scalp EEG data are ambiguous or contradictory, PET provides a less invasive means than chronic grid or depth electrode recording for evaluating whether a localized epileptogenic area exists.
对8名因顽固性癫痫接受皮质切除术的儿童(年龄在13个月至12岁之间)进行了研究,以探讨正电子发射断层扫描(PET)显示的葡萄糖利用局灶性紊乱与术中皮质脑电图(ECoG)定义的电生理异常之间的关系。这些儿童均无单纯颞叶癫痫。8名儿童中有4名的计算机断层扫描(CT)和/或磁共振成像(MRI)结果正常。头皮脑电图(EEG)显示,所有8名儿童的发作间期均有侧化癫痫样异常,8名中有5名发作起始侧化。7名儿童的发作间期PET显示局灶性代谢减低;第8名儿童有局灶性发作期代谢增高。手术时的ECoG显示癫痫样棘波、慢波和/或正常背景活动抑制,在每种情况下均与PET扫描上的病灶相对应。ECoG结果支持以下观点:在癫痫儿童中,PET上的局灶性代谢异常对应于皮质的电生理异常区域,这些区域大概也是致痫区域。这些区域在解剖学成像研究(CT和MRI)上可能显示正常。当发作期头皮EEG数据不明确或相互矛盾时,PET提供了一种比慢性格栅或深部电极记录侵入性更小的方法,用于评估是否存在局限性致痫区域。