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RADIOLOGY QUIZ
DR. FARRUKH JAVEED
• 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.
Hounsfield Units On CT Scan
DIFFERENTIALS
• Oligodendroglioma
• AV Malformation
• Astrocytoma
• Calcified Tuberculoma
• Atypical Meningioma
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.
WHO CLASSIFICATION: GLIOMA
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
SMITH GRADING
1. Nuclear/Cytoplasmic Ratio
2. Maximal Cell Density
3. Pleomorphism
4. Endothelial Proliferation
5. Necrosis
• Grade A: 94 months
• Grade B: 51 months
• Grade C: 45 months
• Grade D: 17 months
CT SCAN
• Plain CT Scan: Mixed density
(hypodense to isodense). Calcifications
90%
• Contrast CT: 50% of
oligodendrogliomas enhance.
MRI T1WI: Hypointense
MRI T2WI: Hyperintense (except
calcified areas)
FLAIR: Hyperintense
T1 + CONTRAST: Heterogeneous
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.
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
PROGNOSIS
• Better Prognosis:
– Pure ODGs
– Calcified ODGs
– Frontal lobe ODGs
– Chromosomal 1p and 19q loss
THANK YOU….

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Radiology quiz - Oligodendroglioma

  • 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.
  • 4. DIFFERENTIALS • Oligodendroglioma • AV Malformation • Astrocytoma • Calcified Tuberculoma • Atypical Meningioma
  • 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
  • 8. SMITH GRADING 1. Nuclear/Cytoplasmic Ratio 2. Maximal Cell Density 3. Pleomorphism 4. Endothelial Proliferation 5. Necrosis • Grade A: 94 months • Grade B: 51 months • Grade C: 45 months • Grade D: 17 months
  • 9. CT SCAN • Plain CT Scan: Mixed density (hypodense to isodense). Calcifications 90% • Contrast CT: 50% of oligodendrogliomas enhance.
  • 11. MRI T2WI: Hyperintense (except calcified areas)
  • 13. T1 + CONTRAST: Heterogeneous
  • 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
  • 16. PROGNOSIS • Better Prognosis: – Pure ODGs – Calcified ODGs – Frontal lobe ODGs – Chromosomal 1p and 19q loss