2. • 36 years old male shopkeeper presents
with Sudden loss of
consciousness.
• Hx of multiple episodes of seizures in
last 2 years, previous episode was 3
months back.
• No hx of headache or any other
neurological deficit. No previous hx of
head trauma.
5. OLIGODENDROGLIOMA
• 2-4 % of primary brain tumors
• Male:Female 3:2
• Average age 40 years
• Usual presentation is seizures for many years prior to the diagnosis.
• Seizures are the presenting symptoms in 50-80% of cases.
• Frontal lobe is the commonest location.
• Calcifications:
– 28-60% on plain radiographs
– 90% on CT scans.
7. PATHOLOGY
• Usually solid tumors
• 16% have the cystic component.
• "fried egg" appearance under the light microscope due to perinuclear halos.
• 33-41% have some component of ependymal or neoplastic astrocytic cells
(oligoastrocytomas or mixed gliomas).
• Grading:
– Low grade (WHO grade II): Oligodendroglioma
– High grade (WHO grade III): Anaplastic oligodendroglioma
14. MRI
• T1: hypointense
• T2: hyperintense (except calcified
areas)
• T1 Contrast (Gd): contrast
enhancement is common usually
heterogeneous when present but it is
not a reliable indicator of tumor grade.
15. TREATMENT
• Chemotherapy:
– PCV [Procarbazine, CCNU (Lomustine) and Vincristine]
– Most ODGs respond to chemotherapy in less than 3 months often with a reduction
in size.
– Chromosome 1p & 19q loss shows good response to chemo and better prognosis.
• Surgery:
– ODGs with significant mass effect
– Resectable low grade ODGs
– High grade ODGs