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[Tuberous sclerosis: case report with histopathological and ultrastructural study].

作者信息

Reis Filho J S, Montemór Netto M R, Loyola Netto J G, de Araújo J C, Antoniuk S, Torres L F

机构信息

Serviço de Anatomia Patológica (SAP), Hospital das Clínicas da Universidade Federal do Paraná (HC/UFPR), Curitiba PR, Brasil.

出版信息

Arq Neuropsiquiatr. 1998 Sep;56(3B):671-6.

PMID:9850769
Abstract

Tuberous sclerosis complex is a group of autosomal disorders characterized by hamartomas and benign neoplastic lesions that invariably affect the central nervous system. We report a case of tuberous sclerosis that is the first presenting ultrastructural findings of this phacomatosis in the Latin American literature. The patient was a 2 year old girl presenting West syndrome non responsive to the clinical treatment with vigabatrin, trileptal and clonazepan, and undergoing left frontal lobectomy. The histopathological and ultrastructural findings were compatible with tuberous sclerosis. These results may help to further understand this controversial phacomatosis, warning to the clinical presentation as West syndrome.

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