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伴有中央颞区棘波的儿童良性癫痫失张力型变体(失张力型BECTS):一种独特的电临床综合征。

Atonic variant of benign childhood epilepsy with centrotemporal spikes (atonic-BECTS): a distinct electro-clinical syndrome.

作者信息

Cherian Ajith, Baheti Neeraj N, Menon Ramshekhar N, Iyer Rajesh S, Rathore Chaturbhuj, Radhakrishnan Ashalatha

机构信息

Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.

出版信息

Brain Dev. 2012 Jun;34(6):511-9. doi: 10.1016/j.braindev.2011.09.007. Epub 2011 Oct 7.

Abstract

PURPOSE

To describe the clinical and electroencephalographic features, treatment strategies and outcome in a series of children with the atonic variant of benign childhood epilepsy with centrotemporal spikes (atonic-BECTS).

MATERIAL AND METHODS

Out of the 148 patients with BECTS reviewed from January 2005 to June 2010 in our Institute, there were seven (5%) with atonic-BECTS. All underwent video EEG, high-resolution magnetic resonance imaging (MRI), neuropsychological evaluation and language assessment. Their progress was followed. In addition to sodium valproate, three were treated with steroids, followed by intravenous immunoglobulin (IVIG) when the seizures relapsed while tapering or after stopping the steroids.

RESULTS

All of the children had earlier onset (mean=2.4 years), increased frequency and increased duration of focal seizures compared to typical BECTS. Head drop and truncal sway due to axial or axiorhizomelic atonia occurring several times per day or week was the key manifestation. The atonic seizures worsened with carbamazepine in three, clonazepam in two and clobazam in one. When the atypical seizures commenced, some children developed one or more of the following problems: hyperactivity, attention deficit, clumsy gait, and mild cognitive or language dysfunction. Three children became seizure free, one on steroids and the other two on IVIG.

CONCLUSIONS

BECTS in children with an early age of onset and frequent and prolonged seizures is more likely to evolve into atonic-BECTS. Carbamazepine and some benzodiazepines may worsen these seizures. Three children became seizure free with immunomodulatory therapy, one on steroids and the other two on IVIG, and had complete resolution of the transient motor and cognitive impairment. Atonic-BECTS needs to be differentiated from Lennox-Gastaut syndrome since it is potentially treatable and children recover with no sequel. Although all the children in this series continued to be on treatment with sodium valproate it is currently undetermined whether they would have required to do so if followed up for an extended period of time.

摘要

目的

描述一系列具有中央颞区棘波的良性儿童癫痫失张力型(失张力性BECTS)患儿的临床和脑电图特征、治疗策略及预后。

材料与方法

2005年1月至2010年6月在我院复查的148例BECTS患者中,有7例(5%)为失张力性BECTS。所有患者均接受了视频脑电图、高分辨率磁共振成像(MRI)、神经心理学评估和语言评估,并对其病情进展进行了随访。除丙戊酸钠外,3例患者接受了类固醇治疗,在逐渐减量或停用类固醇时癫痫复发,随后接受静脉注射免疫球蛋白(IVIG)治疗。

结果

与典型BECTS相比,所有患儿起病较早(平均2.4岁),局灶性癫痫发作频率增加、持续时间延长。每天或每周出现数次因轴性或轴根性失张力导致的头部下垂和躯干摇摆是关键表现。3例患者使用卡马西平、2例使用氯硝西泮、1例使用氯巴占后失张力性癫痫发作加重。非典型癫痫发作开始时,一些患儿出现以下一种或多种问题:多动、注意力缺陷、步态笨拙以及轻度认知或语言功能障碍。3例患儿癫痫发作停止,1例使用类固醇,另外2例使用IVIG。

结论

起病早且癫痫发作频繁、持续时间长的儿童BECTS更有可能演变为失张力性BECTS。卡马西平和一些苯二氮䓬类药物可能会使这些癫痫发作加重。3例患儿通过免疫调节治疗癫痫发作停止,1例使用类固醇,另外2例使用IVIG,短暂的运动和认知障碍完全消失。失张力性BECTS需要与Lennox-Gastaut综合征相鉴别,因为它有潜在的可治疗性,患儿康复后无后遗症。尽管本系列中的所有患儿仍继续使用丙戊酸钠治疗,但如果长期随访,目前尚不确定他们是否需要继续治疗。

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