Yang Zhixian, Liu Xiaoyan, Qin Jiong, Zhang Yuehua, Bao Xinhua, Chang Xingzhi, Wang Shuang, Wu Ye, Xiong Hui
Department of Pediatrics, Peking University First Hospital, No. 1 Xi'anmen Street, Xicheng District, Beijing, PR China.
Brain Dev. 2009 Apr;31(4):274-81. doi: 10.1016/j.braindev.2008.04.004. Epub 2008 Jun 17.
To investigate the clinical and neurophysiological characteristics, particularly therapeutic considerations, of epileptic negative myoclonus (ENM) in atypical benign partial epilepsy (ABPE) of childhood.
From 1998 to 2006, 14/242 patients with benign children epilepsy with centrotemporal spikes (BECTS) were diagnosed as having ABPE with ENM. In all 14 patients, we performed video-EEG monitoring along with tests with the patient's arms outstretched; 6/14 patients were also simultaneously underwent surface electromyogram (EMG). ENM manifestations, electrophysiological features, and responses to antiepileptic drugs were analyzed.
In all cases, ENM developed after the onset of epilepsy and during antiepileptic drug therapy, and the appearance of ENM were corresponding to EEG findings of high-amplitude spikes followed by a slow wave in the contralateral motor areas with secondary generalization. This was further confirmed by time-locked silent EMG. During ENM occurrence or recurrence, habitual seizures and interictal discharges were exaggerated. In some patients, the changes in antiepileptic drug regimens in relation to ENM appearance included add-on therapy with carbamazepine, oxcarbazepine, and phenobarbital or withdrawal of valproate. ENM was controlled in most cases by administration of various combinations of valproate, clonazepam, and corticosteroids.
The incidence of ENM or ABPE in our center was approximately 5.79%. A combination of video-EEG monitoring with the patient's arms outstretched and EMG is essential to identify ENM. The aggravation of habitual seizures and interictal discharges indicate ENM. Some antiepileptic drugs, such as carbamazepine, oxcarbazepine, and phenobarbital, may be related to ENM occurrence during spontaneous aggravation of ABPE. Various combinations of valproate, benzodiazepines, and corticosteroids are relatively effective for treating ENM that occurs in ABPE.
探讨儿童非典型良性部分性癫痫(ABPE)中癫痫性负性肌阵挛(ENM)的临床和神经生理学特征,尤其是治疗方面的考虑因素。
1998年至2006年期间,242例伴有中央颞区棘波的良性儿童癫痫(BECTS)患者中有14例被诊断为ABPE合并ENM。对这14例患者均进行了视频脑电图监测,同时让患者伸展双臂进行测试;14例患者中有6例还同步进行了表面肌电图(EMG)检查。分析了ENM的表现、电生理特征及对抗癫痫药物的反应。
在所有病例中,ENM在癫痫发作后及抗癫痫药物治疗期间出现,其出现与对侧运动区高波幅棘波后跟随慢波并继发泛化的脑电图表现相对应。时间锁定的静息肌电图进一步证实了这一点。在ENM发作或复发期间,习惯性发作和发作间期放电会加剧。在一些患者中,与ENM出现相关的抗癫痫药物治疗方案的改变包括加用卡马西平、奥卡西平、苯巴比妥或停用丙戊酸盐。大多数情况下,通过丙戊酸盐、氯硝西泮和皮质类固醇的各种联合应用可控制ENM。
我们中心ENM或ABPE的发生率约为5.79%。视频脑电图监测结合患者伸展双臂及肌电图检查对于识别ENM至关重要。习惯性发作和发作间期放电加剧提示ENM。一些抗癫痫药物,如卡马西平、奥卡西平、苯巴比妥,可能与ABPE自然加重期间ENM的发生有关。丙戊酸盐、苯二氮䓬类药物和皮质类固醇的各种联合应用对治疗ABPE中出现的ENM相对有效。