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神经节神经胶质瘤的内在致痫性可能与同时存在的局灶性皮质发育不良无关。

Intrinsic epileptogenicity of gangliogliomas may be independent from co-occurring focal cortical dysplasia.

机构信息

Pediatric Neurology Unit, Children's Hospital Meyer-University of Florence, viale Pieraccini 24, 50139 Florence, Italy.

出版信息

Epilepsy Res. 2011 Nov;97(1-2):208-13. doi: 10.1016/j.eplepsyres.2011.07.004. Epub 2011 Aug 9.

Abstract

Gangliogliomas are a frequent cause of drug-resistant epilepsies in children. It remains unknown, however, whether gangliogliomas are intrinsically epileptogenic or if associated lesions contribute to their high epileptogenicity, i.e. associated focal cortical dysplasia (FCD). We report on a child operated twice for drug-resistant focal seizures symptomatic of a right temporal lobe lesion. Histological examination of the first, incomplete lesionectomy revealed tumor-associated FCD Type IIIb. The child was not seizure-free, and surface as well as intracerebral recordings were obtained during a second presurgical assessment. Histopathological examination of the second operation revealed a ganglioglioma. Intralesional EEG recordings from the ganglioglioma documented rhythmic bursts of fast activity suggesting that the high epileptogenicity of gangliogliomas is related to intrinsic epileptogenic activity.

摘要

神经节细胞瘤是儿童药物难治性癫痫的常见病因。然而,目前尚不清楚神经节细胞瘤是否具有内在的致痫性,还是相关病变导致其高致痫性,即相关局灶性皮质发育不良(FCD)。我们报告了一例因右侧颞叶病变引起的药物难治性局灶性癫痫发作而接受两次手术的儿童病例。第一次不完全肿瘤切除术的组织学检查显示与肿瘤相关的 FCD Ⅲb 型。患儿并未无癫痫发作,在第二次术前评估期间进行了表面和脑内记录。第二次手术的组织病理学检查显示为神经节细胞瘤。神经节细胞瘤内的脑电图记录显示快速活动的节律性爆发,表明神经节细胞瘤的高致痫性与内在的致痫性活动有关。

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