Cerebral Malignant Nerve Sheath Tumor, Triton Tumor Variant: Case Report

Author:

Bornstein-Quevedo Leticia1,Peralta-Olvera Fabiola2,Marhx-Bracho Alfonso2,Rodríguez-Jurado Rodolfo1,de Leon-Bojorge Beatriz1

Affiliation:

1. Department of Pathology, Instituto Nacional de Pediatría, Insurgentes Sur #3700-C, Col. Insurgentes Cuicuilco, 04530, Mexico City, D.F., Mexico

2. Department of Neurosurgery, Instituto Nacional de Pediatría, Insurgentes Sur #3700-C, Col. Insurgentes Cuicuilco, 04530, Mexico City, D.F., Mexico

Abstract

A case of a cerebral malignant triton tumor in a 3-year-old boy with a 2-month history of frontal headache and no clinical evidence of neurofibromatosis is reported. The computed tomography (CT) scan showed a large, irregular tumor in the right parietooccipital lobe. A partial surgical resection was performed. Histologically, the tumor was highly cellular and consisted of spindle cells with hyperchromatic and pleomorphic nuclei. Focally, neoplastic cells with rhabdomyoblastic features were found. The immunohistochemical study showed that tumor cells were positive for S-100 protein and CD57, and the rhabdomyoblasts expressed desmin, Myo-D1, and myoglobin. During the postoperative period, a massive intraparenchymal hemorrhage was identified and surgical drainage was performed. The patient worsened and died 10 days after the first surgery. Postmortem study was not authorized. Six cases of cerebral malignant nerve sheath tumor have been described; however, primary intraparenchymal malignant triton tumor has not been previously described.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

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