Raso Pedro, Tafuri Alexandre, Lopes Ney da Fonseca, Monteiro Eduardo Rossi, Tafuri Wagner Luiz
Departamento de Anatomia Patológica e Medicina Legal, Faculdade de Medicina, Universidade Federal de Minas Gerais, Rua Sao Paulo 893, 30170-131 Belo Horizonte, MG.
Rev Soc Bras Med Trop. 2006 May-Jun;39(3):283-6. doi: 10.1590/s0037-86822006000300012.
An unusual case of the tumoral form of cerebellar Schistosomiasis mansoni, in a 15 year-old male diagnosed by biopsy, with neurological signs and symptoms 60 days prior to surgery. Computerized tomography show a hyperdense expanding lesion located in cerebellum, suggesting glioma. Histopathological examination showed numerous S. mansoni ova involved by granulomatous inflammation in necrotic-exudative phase, located mainly in the internal, granular layer of the cerebellum, creating a pseudotumor in the cerebellar vermis and a recent hemorrhage in the trunk. The areas of granulomas were measured.
一名15岁男性患曼氏血吸虫病小脑肿瘤型的罕见病例，术前60天出现神经体征和症状，经活检确诊。计算机断层扫描显示小脑有一个高密度的扩张性病变，提示为胶质瘤。组织病理学检查显示，在坏死渗出期，大量曼氏血吸虫卵被肉芽肿性炎症累及，主要位于小脑的内颗粒层，在小脑蚓部形成假肿瘤，在躯干处有近期出血。对肉芽肿区域进行了测量。
