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慢波睡眠期的认知功能衰退与电持续状态癫痫

Cognitive deterioration and electrical status epilepticus during slow sleep.

作者信息

Scholtes F B J, Hendriks M P H, Renier W O

机构信息

Gemini Hospital, Den Helder, The Netherlands.

出版信息

Epilepsy Behav. 2005 Mar;6(2):167-73. doi: 10.1016/j.yebeh.2004.11.001.

Abstract

The results of long-term follow-up of 10 children with global or specific cognitive deterioration and, on the electroencephalogram, electrical status epilepticus during sleep (ESES) are described. They were referred because of cognitive deterioration and underwent repeated neurological and neuropsychological examinations and all-night electroencephalography. A previous cognitive level was known or could be estimated in all. Seven children had a continuous spikes and waves during sleep (CSWS) syndrome, with global cognitive deterioration in four and more specific cognitive decline in three, and another three children had Landau-Kleffner syndrome (LKS). Of the last three, two children never had seizures, while the other had localization-related epilepsy. No children experienced aggravation of clinical seizures. However, therapy was disappointing. Cognitive dysfunction did not respond to valproate and/or benzodiazepines in 9 of the 10 children. A frontal epileptic focus was found in 5 of 7 children with CSWS, and a left temporal focus in 2 of 3 children with LKS. The ESES persisted in CSWS for 5-9 years and in LKS for 1-5 years, and disappeared at puberty. Good cognitive recovery after disappearance of ESES occurred in only one child, and partial recovery in four. An unfavorable prognosis of cognitive deterioration seems to be related to long-duration ESES and/or early onset epileptic activity. The authors are of the opinion that cognitive deterioration in children, with or without manifest epileptic seizures, should mandate electroencephalographic investigation during sleep.

摘要

本文描述了10例患有全面性或特异性认知功能衰退且脑电图显示睡眠期癫痫性电持续状态(ESES)的儿童的长期随访结果。他们因认知功能衰退前来就诊,并接受了多次神经学和神经心理学检查以及整夜脑电图检查。所有人之前的认知水平均已知或可估算。7名儿童患有睡眠期持续性棘慢波(CSWS)综合征,其中4名出现全面性认知衰退,3名出现更具特异性的认知功能下降,另外3名儿童患有Landau-Kleffner综合征(LKS)。在最后这3名儿童中,2名从未发生过癫痫发作,另1名患有局灶性相关性癫痫。所有儿童的临床癫痫发作均未加重。然而,治疗效果令人失望。10名儿童中有9名的认知功能障碍对丙戊酸盐和/或苯二氮䓬类药物无反应。7名患有CSWS的儿童中有5名发现额叶癫痫病灶,3名患有LKS的儿童中有2名发现左侧颞叶病灶。ESES在CSWS中持续5 - 9年,在LKS中持续1 - 5年,并在青春期消失。ESES消失后,仅有1名儿童实现了良好的认知恢复,4名儿童部分恢复。认知功能衰退的不良预后似乎与ESES持续时间长和/或癫痫活动早发有关。作者认为,无论有无明显癫痫发作,儿童出现认知功能衰退均应进行睡眠期脑电图检查。

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