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P. R. health sci. j ; 22(4): 401-404, Dec. 2003.
Article in English | LILACS | ID: lil-358562

ABSTRACT

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.


Subject(s)
Humans , Male , Child, Preschool , Brain Neoplasms/pathology , Rhabdoid Tumor/pathology , Immunohistochemistry , Brain Neoplasms , Brain Neoplasms/therapy , Neurosurgical Procedures/methods , Tomography, X-Ray Computed , Treatment Outcome , Rhabdoid Tumor , Rhabdoid Tumor/therapy
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