Ichimiya Yuko, Kaku Noriyuki, Sanefuji Masafumi, Torio Michiko, Mizuguchi Soichi, Motomura Yoshitomo, Muraoka Mamoru, Lee Sooyoung, Baba Haruhisa, Sonoda Yuri, Ishizaki Yoshito, Sasazuki Momoko, Sakai Yasunari, Maehara Yoshihiko, Ohga Shouichi
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; Emergency and Critical Care Center, Kyushu University Hospital, Fukuoka, Japan.
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; Research Center for Environment and Developmental Medical Sciences, Kyushu University, Fukuoka, Japan.
Epilepsy Res. 2018 Jul;143:70-74. doi: 10.1016/j.eplepsyres.2018.04.006. Epub 2018 Apr 11.
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a newly defined clinicoradiologic syndrome characterized by biphasic seizures and altered consciousness followed by restricted diffusion in the white matter on magnetic resonance imaging in acute phase. Intractable epilepsy commonly occurs as the late complication. This study aimed to search predisposing factors to the development of epilepsy after AESD. Consecutively treated 22 patients with AESD in our institution from 2006 to 2016 were grouped into those with post-encephalopathic epilepsy (PEE, n = 10) or without PEE (n = 12). There was no difference between two groups in age at the onset of AESD, duration of the initial seizures, or the follow-up periods after discharge. PEE group patients more frequently showed coma or involuntary movements during the course of AESD than non-PEE group patients (36% vs. 8%, p = 0.008). The quantitative analysis of apparent diffusion coefficient (ADC) map revealed that PEE group showed broader areas with reduced diffusion in the posterior lobes at the onsets of AESD than non-PEE group (0.113 vs. 0.013, p = 0.035). On the other hand, the atrophy on day 30-ADC map did not correlate with the development or control of epilepsy. These results suggest that the clinical severity and ADC profiles in acute phase, rather than the brain atrophy in convalescent phase, may predict the development of post-AESD epilepsy.
伴双相性癫痫发作和晚期弥散受限的急性脑病(AESD)是一种新定义的临床放射学综合征,其特征为双相性癫痫发作和意识改变,随后在急性期磁共振成像显示白质弥散受限。难治性癫痫常作为晚期并发症出现。本研究旨在探寻AESD后癫痫发生的易感因素。2006年至2016年在我们机构连续接受治疗的22例AESD患者被分为有脑病后癫痫(PEE,n = 10)或无PEE(n = 12)两组。两组在AESD发病年龄、初始癫痫发作持续时间或出院后随访时间方面无差异。PEE组患者在AESD病程中比非PEE组患者更频繁地出现昏迷或不自主运动(36%对8%,p = 0.008)。表观弥散系数(ADC)图的定量分析显示,PEE组在AESD发作时后叶弥散受限区域比非PEE组更广泛(0.113对0.013,p = 0.035)。另一方面,30天ADC图上的萎缩与癫痫的发生或控制无关。这些结果表明,急性期的临床严重程度和ADC特征,而非恢复期的脑萎缩,可能预测AESD后癫痫的发生。