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儿童癫痫手术候选者中的自闭症谱系障碍

Autistic spectrum disorders in childhood epilepsy surgery candidates.

作者信息

Taylor D C, Neville B G, Cross J H

机构信息

Neurosciences Unit, Institute of Child Health and Great Ormond St. Hospital for Children NHS Trust, Mecklenburgh Sq., UK-London WCI 2AP.

出版信息

Eur Child Adolesc Psychiatry. 1999 Sep;8(3):189-92. doi: 10.1007/s007870050128.

Abstract

One third of children with autistic spectrum disorders (or pervasive developmental disorders) enter that state by regression from a more normal prior development at the onset of epilepsy or epileptiform abnormality in the electroencephalogram. In a very small proportion structural lesions of the temporal lobes are discovered. These form part of the sample of children coming to a surgical treatment programme. Ninety-eight child candidates for epilepsy surgery were seen by one neuropsychiatrist. Their psychiatric diagnoses were coded on DSM IV schedules. Other variables of interest were the age at onset of epilepsy; the nature, the side, and time of acquisition of the lesion; intelligence, and sex. There were 19 children with autistic spectrum disorders including eight with Asperger's syndrome. Ten of the children in the autistic group had right brain lesions; six were dysembryoplastic neuroepithelial tumours (DNETs); two were cortical dysplasias; one tuberous sclerosis; one hemi-cortical defect; and 1 mesial temporal sclerosis. Nine started epilepsy in their first year; nine had IQs in the retarded range; nine of the 11 were male. Six of eight Asperger's children had right brain lesions; two DNETs; four mesial temporal sclerosis; one Rasmussen encephalitis. Four started epilepsy in their first year; one was retarded; five were female. Children who had no, or other, psychiatric disorder also showed "mass" lesions, or temporal sclerosis but with different biases as to side, sex, and very early onset of epilepsy from the autistic spectrum group. Very early onset of epilepsy, with lesions of embryonal origin, in the right temporal lobe, strongly predisposed males towards autistic regression. Such patients should be referred very early for consideration of urgent surgical treatment.

摘要

三分之一的自闭症谱系障碍(或广泛性发育障碍)儿童是在癫痫发作或脑电图出现癫痫样异常时,从先前较为正常的发育状态退化而进入该状态的。在极小比例的儿童中发现了颞叶的结构性病变。这些儿童构成了接受外科治疗计划的样本的一部分。一位神经精神科医生诊治了98名癫痫手术候选儿童。他们的精神科诊断按照《精神疾病诊断与统计手册》第四版的标准进行编码。其他感兴趣的变量包括癫痫发作的起始年龄;病变的性质、部位和形成时间;智力以及性别。其中有19名患有自闭症谱系障碍的儿童,包括8名患有阿斯伯格综合征的儿童。自闭症组中有10名儿童右脑有病变;6名是胚胎发育不良性神经上皮瘤(DNETs);2名是皮质发育异常;1名是结节性硬化症;1名是半皮质缺损;还有1名是内侧颞叶硬化。9名儿童在第一年就开始癫痫发作;9名儿童的智商处于智力迟钝范围;11名中有9名是男性。8名阿斯伯格综合征儿童中有6名右脑有病变;2名是DNETs;4名是内侧颞叶硬化;1名是拉斯穆森脑炎。4名儿童在第一年就开始癫痫发作;1名智力迟钝;5名是女性。没有精神疾病或患有其他精神疾病的儿童也显示出“块状”病变或颞叶硬化,但在病变部位、性别以及癫痫发作极早期方面与自闭症谱系障碍组存在不同倾向。癫痫发作极早期,伴有胚胎起源的病变,且位于右侧颞叶,这使得男性极易出现自闭症退化。这类患者应尽早转诊,以便考虑进行紧急外科治疗。

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