• Well-differentiated, slowly growing but diffusely infiltrating
• Most common site is frontal lobe (50-65%)
• Best diagnostic clue: Partially calcified subcortical/cortical
frontal mass in middle-aged adult
○ Typically T2 heterogeneous, hyperintense mass
○ Heterogeneous enhancement is typical
• New enhancement in previously nonenhancing
oligodendroglioma suggests malignant progression
• Anaplastic oligodendroglioma
• Low-grade diffuse astrocytoma
• Dysembryoplastic neuroepithelial tumor
• Pleomorphic xanthoastrocytoma
• Loss of heterozygosity for 1p and 19q (50-70%)
• Anaplastic oligodendroglioma = WHO grade III
• Oligodendrogliomas carry better prognosis than
• 5-10% of primary intracranial neoplasms
• Seizures, headaches, and focal neurologic deficits are most
• Peak incidence: 4th and 5th decades
• Median survival time = 10 years
• 1p, 19q deletions and IDH1(+) associated with more
heterogeneous cystic and solid
shows a large, calcified, left
calcification. The calcification
the frontal gyri ſt. The frontal
of both cortex and subcortical
Differentiating a grade II from
perfusion may help predict the
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