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伴有室管膜下结节性异位、皮质发育异常和癫痫的前脑膨出:病例报告及文献复习

Anterior encephalocele associated with subependymal nodular heterotopia, cortical dysplasia and epilepsy: case report and review of the literature.

作者信息

Rojas Luisa, Melvin Joseph J, Faerber Eric N, Valencia Ignacio

机构信息

Department of Neurology, Hahnemann University Hospital, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

Eur J Paediatr Neurol. 2006 Sep-Nov;10(5-6):227-9. doi: 10.1016/j.ejpn.2006.08.010. Epub 2006 Oct 10.

Abstract

The presence of subependymal nodular heterotopia and cortical dysgenesis has been infrequently reported in patients with encephalocele. The majority of these patients were found to have posterior encephaloceles. We report a case of a Hispanic female with a frontoethmoidal encephalocele who developed epilepsy at 15 years of age. Magnetic resonance imaging of the brain demonstrated left subependymal nodular heterotopia, partial agenesis of the corpus callosum and left fronto-temporal cortical dysplasia with polymicrogyria. This case illustrates the association of anterior encephalocele with subependymal nodular heterotopia, cortical dysplasia and epilepsy. It underscores the importance of screening for intracranial abnormalities in patients with anterior encephalocele.

摘要

室管膜下结节性异位和皮质发育异常在脑膨出患者中的报道较少。这些患者大多被发现患有后脑膨出。我们报告一例患有额筛部脑膨出的西班牙裔女性病例,该患者在15岁时出现癫痫。脑部磁共振成像显示左侧室管膜下结节性异位、胼胝体部分发育不全以及左侧额颞叶皮质发育异常伴多小脑回。该病例说明了前脑膨出与室管膜下结节性异位、皮质发育异常和癫痫之间的关联。它强调了对前脑膨出患者进行颅内异常筛查的重要性。

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