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
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.