Malignant glial tumor arising from the site of a previous hamartoma/ganglioglioma: Coincidence or malignant transformation?

Citation
Ma. Mittler et al., Malignant glial tumor arising from the site of a previous hamartoma/ganglioglioma: Coincidence or malignant transformation?, PED NEUROS, 30(3), 1999, pp. 132-134
Citations number
14
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC NEUROSURGERY
ISSN journal
10162291 → ACNP
Volume
30
Issue
3
Year of publication
1999
Pages
132 - 134
Database
ISI
SICI code
1016-2291(199903)30:3<132:MGTAFT>2.0.ZU;2-E
Abstract
That the originally resected gangliogliomascreening are generally considere d benign tumors. Although more commonly found in the brain, spinal cord gan glioglioma is a well established, albeit infrequent, entity. We describe a 2-decade clinical course of a patient initially diagnosed with a thoracolum bar 'glial-neuronal hamartoma' at age 4. Seventeen years after his first op eration, local recurrence was noted. Despite subsequent multiple gross tota l resections and adjuvant therapy, histologic features became increasingly ominous and ultimately proved fatal. This is an unusual report and histolog ic presentation of a resected spinal cord ganglioglioma recurring as an ana plastic ependymoma/astrocytoma and subsequently a glioblastoma. It was actu ally part of a primitive neuroectodermal tumor which had undergone extensiv e maturation.