Trinka E, Dubeau F, Andermann F, Bastos A, Hui A, Li L M, Köhler S, Olivier A
Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Epileptic Disord. 2000 Sep;2(3):153-62.
The aim of this study is to characterize the clinical features and prognostic factors for intractable, post-encephalitic epilepsy.
We studied retrospectively 42 patients (26 men) evaluated between 1982 and 1999. MRI, neuropsychological findings, interictal and ictal scalp EEG were reviewed for all patients. Fifteen patients had additional stereo EEG (SEEG) studies.
The mean age at encephalitis was 17 years (SD = 15.5); etiology was identified in 18 patients. During the acute illness, 79% had status epilepticus (SE) or recurrent seizures and 76% were in coma; mean Glasgow outcome scale (GOS) was 3.6 (SD = 0.8). The mean latency to seizure onset was 0.8 years (SD = 1.9). The majority (72%) presented with complex partial seizures with or without secondary generalization. According to interictal epileptiform findings and the predominant seizure onset pattern as found on scalp EEG, patients were unilateral temporal (UTLE) = 8, bilateral temporal (BTLE) = 12, and extratemporal/multifocal or generalized (ETMFE) = 22 patients. MRI atrophy and/or signal changes were unilateral temporal in 7 (18%), bilateral temporal in 5 (13%), multilobar/diffuse in 20 (51%), and absent in 7 (18%). ANOVA revealed significant differences in mean GOS between UTLE versus BTLE and ETMFE (4.7 versus 3.2 versus 3.6; p < 0.0001), but not in age at encephalitis. Latency to the first unprovoked seizure was shorter in patients with ETMFE compared to UTLE and BTLE (p < 0.01). Surgery was performed in 24 patients. The best outcome was obtained in UTLE (7/8 class I and II). In the others, outcome was poor in the majority (13/16 class III and IV).
There is a small subgroup of patients with postencephalitic UTLE for whom the outcome is favorable. The majority of our patients had multifocal seizure onset with BTLE and ETMFE, and poor outcome after surgical treatment.
本研究旨在描述难治性脑炎后癫痫的临床特征和预后因素。
我们回顾性研究了1982年至1999年间评估的42例患者(26例男性)。对所有患者的MRI、神经心理学检查结果、发作间期和发作期头皮脑电图进行了回顾。15例患者还进行了立体脑电图(SEEG)检查。
脑炎发病时的平均年龄为17岁(标准差=15.5);18例患者明确了病因。在急性疾病期间,79%的患者有癫痫持续状态(SE)或反复发作,76%的患者昏迷;平均格拉斯哥预后评分(GOS)为3.6(标准差=0.8)。癫痫发作开始的平均潜伏期为0.8年(标准差=1.9)。大多数患者(72%)表现为复杂部分性发作,伴或不伴有继发性全身性发作。根据发作间期癫痫样放电表现和头皮脑电图上发现的主要发作起始模式,患者分为单侧颞叶癫痫(UTLE)=8例、双侧颞叶癫痫(BTLE)=12例、颞叶外/多灶性或全身性癫痫(ETMFE)=22例。MRI萎缩和/或信号改变单侧颞叶受累7例(18%)、双侧颞叶受累5例(13%)、多叶/弥漫性受累20例(51%)、无改变7例(18%)。方差分析显示UTLE与BTLE和ETMFE之间的平均GOS有显著差异(4.7对3.2对3.6;p<0.0001),但脑炎发病年龄无差异。与UTLE和BTLE相比,ETMFE患者首次无诱因发作的潜伏期更短(p<0.01)。24例患者接受了手术治疗。UTLE患者获得了最佳预后(7/8例为I级和II级)。在其他患者中,大多数患者预后较差(13/16例为III级和IV级)。
有一小部分脑炎后UTLE患者预后良好。我们的大多数患者发作起始多灶性,表现为BTLE和ETMFE,手术治疗后预后较差。