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Oligodendroglioma with focal or diffuse histologic features of malignancy
Best diagnostic clue: Calcified frontal lobe mass involving cortex and subcortical white matter
Frontal lobe is most common location, followed by temporal lobe
Majority have nodular or clumped calcification
May see hemorrhage or necrosis
Variable enhancement
Anaplastic oligodendroglioma more likely to enhance than low-grade oligo
Neoplastic cells almost always found beyond areas of abnormal signal intensity
MRS and MR perfusion may help distinguish grade II from grade III oligos
Oligodendroglioma
Anaplastic astrocytoma
Glioblastoma multiforme
Cerebritis
Ischemia
WHO grade III
Oligos: Better prognosis than astrocytomas of same grade
Headache, seizures are most common presentations
Occurs at all ages; mean is 49 years
20-50% of oligodendrogliomas are anaplastic
Median survival: 4 years
5-year survival: 40-45%; 10-year survival: 15%
1p and 19q deletions associated with prolonged survival
Anaplastic oligodendroglioma (AO), high-grade oligodendroglioma (oligo)
Highly cellular, diffusely infiltrating glioma
Oligodendroglioma with focal or diffuse histologic features of malignancy
Best diagnostic clue
Calcified frontal lobe mass involving cortex and subcortical white matter (WM)
Location
Supratentorial hemispheric mass, involves cortex and subcortical WM
Frontal lobe most common, followed by temporal lobe
May involve parietal or occipital lobes
Often expands overlying cortex
Size
Variable
Morphology
Diffusely infiltrative mass
May appear discrete, but always infiltrative
Neoplastic cells almost always found beyond areas of abnormal signal intensity
NECT
Mixed density (hypodense/isodense) mass
Majority calcify, nodular or clumped Ca++
May see gyriform Ca++
Cystic degeneration common
May see hemorrhage or necrosis
May expand, remodel, or erode calvaria
CECT
Variable enhancement
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