[Landau-Kleffner syndrome (acquired aphasia with epilepsy). Etiopathology and response to treatment with anticonvulsants].

M I López-Ibor, J J López-Ibor, M Hernández Herreros
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Abstract

The Landau-Kleffner syndrome consists in the association of an aphasia acquired during childhood or adolescence after a period of normal development, accompanied by epileptic fits and, sometimes, psychological disturbances. The appearance of the symptoms may not be simultaneous. The nature of this syndrome has been widely discussed and even the possibility of being a non-unitary syndrome has been considered. It may be possibly due to diverse etiologies, genetic or acquired (infectious). The relation between the aphasic, the psychologic and the convulsive symptoms has also raised controversies. A case of a female is described in which the psychological symptomatology was so severe, she had to be admitted in a psychiatric unit. The symptoms consisted in agitation during the night and severe persistent insomnia so as difficulties for relationship during day. No abnormalities were detected in a TAC nor in a RM but electroencephalographic and neuropsychological abnormalities were detected. The epileptic fits disappeared with a carbamacepine treatment but the rest of symptoms remained even more accentuated. After her admission, a treatment with valproate achieved to control her fits and the aphasic symptoms and neuropsychological deficits were compensated in the course of several months. After a year of treatment the patient's life was normalized, she resumed her studies, the EEG abnormalities disappeared so as the psychological disturbances and the behavior problems with the exception of phobic symptoms, similar to the ones of other family members. The patient has a history of epilepsy on its mother's side. The evolution and treatment response suggests that at least in some cases of the Landau-Kleffner syndrome, the etiology of the aphasia and other neuropsychological deficits and of the behavior disorders are related with some subclinical epileptic discharges and with a "functional inhibition" of some areas of the nervous system.

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兰多-克莱夫纳综合征(获得性失语伴癫痫)。病因和对抗惊厥药物治疗的反应]。
朗多-克莱夫纳综合征与儿童期或青春期正常发育后获得的失语症有关,伴有癫痫发作,有时还伴有心理障碍。这些症状可能不是同时出现的。该综合征的性质已被广泛讨论,甚至被认为是非酉综合征的可能性。它可能是由于多种病因,遗传或获得性(传染性)。失语、心理和惊厥症状之间的关系也引起了争议。描述了一名女性的案例,其中心理症状非常严重,她不得不住进精神科。症状包括夜间躁动和严重的持续性失眠,白天人际关系困难。TAC和RM均未发现异常,但发现脑电图和神经心理学异常。卡马西平治疗后癫痫发作消失,但其他症状更加严重。入院后,丙戊酸治疗控制了她的发作,失语症状和神经心理缺陷在几个月的时间内得到了补偿。经过一年的治疗,患者生活恢复正常,恢复学业,脑电图异常消失,除恐惧症状外,心理障碍和行为问题消失,与其他家庭成员相似。病人母亲有癫痫史。发展和治疗反应表明,至少在一些兰多-克莱夫纳综合征的病例中,失语和其他神经心理缺陷以及行为障碍的病因与一些亚临床癫痫放电和神经系统某些区域的“功能性抑制”有关。
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