Mixed glioneuronal neoplasms are relatively uncommon tumors in the central
nervous system. Recently, an unusual glioneuronal tumor arising in adults m
arked histologically by neuropil-like islands was described. We present a s
imilar case arising in a 23-year-old woman who presented with headaches and
seizures and on imaging studies was noted to have a frontal-temporal lobe
mass. The patient underwent partial resection of the tumor, which histologi
cally resembled anaplastic astrocytoma, and received a course of radiation
therapy and chemotherapy. increasing seizure frequency and expanding size o
n neuroimaging prompted a re-excision of the tumor. The second resection wa
s marked by islands of tissue resembling gray matter with slightly atypical
neuronal and glial cells situated in the white matter. These islands stain
ed positively with synaptophysin and did not stain with glial fibrillary ac
id protein. Mild vascular proliferation and moderate nuclear pleomorphism a
lso characterized the tumor. Areas of necrosis were not noted, A MIB-1 labe
ling index of 18.1% was noted. P53 immunoreactivity was observed in approxi
mately 40% of tumor cell nuclei, This lesion is felt to represent a clinica
lly aggressive glioneuronal neoplasm with an unusual and distinctive histol
ogic phenotype. HUM PATHOL 31:1435-1438. Copyright (C) 2000 by W.B. Saunder
s Company.