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P. R. health sci. j ; 22(4): 401-404, Dec. 2003.
Artigo em Inglês | LILACS | ID: lil-358562

RESUMO

Rhabdoid tumors of the brain are rare with an invariable dismal prognosis despite treatment. This is the case of a 3 year old boy who presented lethargy, somnolence, nausea, vomiting, and headaches one week prior to hospitalization. A posterior fossa tumor with hydrocephalus was noted on a head computed tomography (CT) scan. A ventriculoperitoneal shunt was placed with subsequent gross total tumor resection. Pathology findings were those of a rhabdoid tumor. The histopathology, immunohistochemistry and ultrastructure of this unusual pediatric cerebral neoplasia is discussed.


Assuntos
Humanos , Masculino , Pré-Escolar , Neoplasias Encefálicas/patologia , Tumor Rabdoide/patologia , Imuno-Histoquímica , Neoplasias Encefálicas , Neoplasias Encefálicas/terapia , Procedimentos Neurocirúrgicos/métodos , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Tumor Rabdoide , Tumor Rabdoide/terapia
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