[Contribution to our knowledge of the Landau and Kleffner "acquired aphasia with epilepsy" syndrome].

A Lorizio, A Franciosi
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引用次数: 0

Abstract

The Authors describe a case of aphasia acquired in childhood together with epilepsy (syndrome of Landau and Kleffner) and treated for seven years. The patient had simple and complex partial attacks, motor dysphasia, frequent and heavy headache, and electroencephalographic paroxysmal anomalies with multifocal distribution. While the disease evolved with regression of disphasia and epilepsy, the EEG alterations persisted. In view of similar cases reported in the literature and the present treatment the Authors feel that syndrome is an inflammatory disease, its evolution being slow. The results of neuroradiological investigations support such hypothesis. The prognosis is poor (anomalies of speech persisted in 2 out of 3) and further studies are essential. A systematic use of cerebral biopsy is suggested.

[对Landau和Kleffner“获得性失语伴癫痫”综合征的认识贡献]。
作者描述了一例儿童期失语合并癫痫(朗道和克莱夫纳综合征)并治疗7年的病例。患者有简单和复杂的部分发作,运动吞咽障碍,频繁和严重的头痛,脑电图阵发性异常,多灶分布。当疾病随着失语症和癫痫的消退而发展时,脑电图改变持续存在。结合文献报道的类似病例和目前的治疗,笔者认为综合征是一种炎症性疾病,其演变缓慢。神经放射学研究结果支持这一假设。预后很差(3例中有2例言语异常),需要进一步研究。建议系统使用脑活检。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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