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Well-differentiated, slowly growing but diffusely infiltrating cortical/subcortical tumor
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
~ 50% enhance
Heterogeneous enhancement is typical
New enhancement in previously nonenhancing oligodendroglioma suggests malignant progression
Anaplastic oligodendroglioma
Low-grade diffuse astrocytoma
Ganglioglioma
Dysembryoplastic neuroepithelial tumor
Pleomorphic xanthoastrocytoma
Cerebritis
Cerebral ischemia
Loss of heterozygosity for 1p and 19q (50-70%)
WHO grade II
Anaplastic oligodendroglioma = WHO grade III
Oligodendrogliomas carry better prognosis than astrocytomas of same grade
5-10% of primary intracranial neoplasms
Seizures, headaches, and focal neurologic deficits are most common presentations
Peak incidence: 4th and 5th decades
Median survival time = 10 years
1p, 19q deletions and IDH1 (+) associated with more favorable prognosis
Well-differentiated, slowly growing, but diffusely infiltrating, cortical/subcortical tumor
Best diagnostic clue
Partially calcified subcortical/cortical mass in middle-aged adults
Location
Typically involves subcortical white matter (WM) and cortex
Majority supratentorial (85%), hemispheric WM
Most common site is frontal lobe (50-65%)
May involve temporal, parietal, or occipital lobes
Rare: Posterior fossa
Extremely rare: Intraventricular, brainstem, spinal cord, primary leptomeningeal
Size
Variable
Morphology
Infiltrative mass that appears well demarcated
NECT
Mixed density (hypo-/isodense) hemispheric mass that extends to cortex
Majority calcify, nodular or clumped Ca++ (70-90%)
Cystic degeneration common (20%)
Hemorrhage, edema are uncommon
May expand, remodel, erode calvaria
CECT
~ 50% enhance
Enhancement varies from none to striking
T1WI
Hemispheric mass, hypo- to isointense to gray matter
Typically heterogeneous
Cortical and subcortical with cortical expansion
May appear well circumscribed with minimal associated edema
T2WI
Typically heterogeneous, hyperintense mass
Heterogeneity related to Ca++, cystic change, less commonly blood products
May appear well circumscribed with minimal associated edema
Typically expands overlying cortex
Hemorrhage, necrosis are rare unless anaplastic
May expand, erode calvaria
FLAIR
Typically heterogeneous, hyperintense
Typically expands overlying cortex
May appear well circumscribed but infiltrative
T2* GRE
Ca++ seen as areas of “blooming”
DWI
No diffusion restriction is typical
T1WI C+
Heterogeneous enhancement is typical
~ 50% enhance
Rarely, leptomeningeal enhancement is seen
MRS
↑ Cho, ↓ NAA
Absence of lipid/lactate peak helps differentiate from anaplastic oligodendroglioma
2HG MRS has been found helpful to identify IDH status
Perfusion MR
Relative cerebral blood volume (rCBV) can help differentiate grade II from grade III
Foci of elevated rCBV can mimic high-grade tumor
SWI: Shows Ca++ as hypointense foci
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