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Imaging Department
Feb 1 9 th
, 20 1 3
Reported by Dr. Giang
 Name: Nong Van Hieu
 Sex: Male
 Age: 5 years old.
 Dept: A13
Clinical
 Headache & vomiting for 1 month
 No fever
 No seizure
 Family’s history: older sister die when 10 years old
because of Epilepsy.
CT Findings
(From Ha Giang Hospital)
 Hyperintense solid mass in 4th
ventricle with edema surround
 Hydrocephalus
 NHP
MRI Findings
(T2WI, axial, Pre C+)
 Hyper-signal & Heterogenous mass in posterior fossa (43x40x49 mm)
 Fill up IV ventricle  Hydrocephalus
 Some necrosis areas
 Vermis invasion.
MRI Findings
(Flair , Coronal, Pre C+)
 Hyper-signal intensity.
 Spherical & well-defined
MRI Findings
(T1WI, Sagital, Pre C+)
 Hypointense to gray matter
 No hemorrhage intra mass
MRI Findings
(Diffusion & ADC)
 Diffusion: Decrease diffusion
 ADC : Hypo signal
 High density of cells
MRI Findings
(T1WI, Axial, Post C+)
 Strong enhancement
 Heterogenous (necrosis areas)
MRI Findings
(T1WI, Sagital, Post C+)
 Strong enhancement
 Heterogenous
MRI Findings
(T1WI, Coronal, Post C+)
 Strong enhancement
 Heterogenous
Diagnosis
Medulloblastoma
Background of MB
 Medulloblastoma: is a highly malignant primary brain tumor that originates
in the cerebellum or posterior fossa. ( PNET-MB)
 Epidemilogy: 15- 20% of all Pediatric brain tumor
30-40% of posterior fossa tumor in children
Rare in adult.
 Location: - 4th
ventricle, arises from roof.
- Cerebellar hemisphere : older children & adult.
 Age: 75% < 10 years. Most diagnosed by 5 year.
 Gender: M > F = 2-4 : 1
 Classification: 4 major PNET-MB subtype
- Classic
- Desmoplastic
- Extensive nodular with advanced neuronal differentiation
- Large cell
Background of MB
 Presentation: - Ataxia , signs of increased intracranial pressure.
(tumor rapid grow)
- Macrocephaly
- Cranial nerve palsies.
 Treatment:
 Surgical excision , adjyvant chemotherapy
 Craniospinal irradiation if > 3 years
 Top differential diagnosis:
 Ependymoma
 Atypical teratoid / rabdoid tumor
Thank you for attention!

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Medulloblastoma

  • 1. Imaging Department Feb 1 9 th , 20 1 3 Reported by Dr. Giang
  • 2.  Name: Nong Van Hieu  Sex: Male  Age: 5 years old.  Dept: A13
  • 3. Clinical  Headache & vomiting for 1 month  No fever  No seizure  Family’s history: older sister die when 10 years old because of Epilepsy.
  • 4. CT Findings (From Ha Giang Hospital)  Hyperintense solid mass in 4th ventricle with edema surround  Hydrocephalus  NHP
  • 5. MRI Findings (T2WI, axial, Pre C+)  Hyper-signal & Heterogenous mass in posterior fossa (43x40x49 mm)  Fill up IV ventricle  Hydrocephalus  Some necrosis areas  Vermis invasion.
  • 6. MRI Findings (Flair , Coronal, Pre C+)  Hyper-signal intensity.  Spherical & well-defined
  • 7. MRI Findings (T1WI, Sagital, Pre C+)  Hypointense to gray matter  No hemorrhage intra mass
  • 8. MRI Findings (Diffusion & ADC)  Diffusion: Decrease diffusion  ADC : Hypo signal  High density of cells
  • 9. MRI Findings (T1WI, Axial, Post C+)  Strong enhancement  Heterogenous (necrosis areas)
  • 10. MRI Findings (T1WI, Sagital, Post C+)  Strong enhancement  Heterogenous
  • 11. MRI Findings (T1WI, Coronal, Post C+)  Strong enhancement  Heterogenous
  • 13. Background of MB  Medulloblastoma: is a highly malignant primary brain tumor that originates in the cerebellum or posterior fossa. ( PNET-MB)  Epidemilogy: 15- 20% of all Pediatric brain tumor 30-40% of posterior fossa tumor in children Rare in adult.  Location: - 4th ventricle, arises from roof. - Cerebellar hemisphere : older children & adult.  Age: 75% < 10 years. Most diagnosed by 5 year.  Gender: M > F = 2-4 : 1  Classification: 4 major PNET-MB subtype - Classic - Desmoplastic - Extensive nodular with advanced neuronal differentiation - Large cell
  • 14. Background of MB  Presentation: - Ataxia , signs of increased intracranial pressure. (tumor rapid grow) - Macrocephaly - Cranial nerve palsies.  Treatment:  Surgical excision , adjyvant chemotherapy  Craniospinal irradiation if > 3 years  Top differential diagnosis:  Ependymoma  Atypical teratoid / rabdoid tumor
  • 15. Thank you for attention!

Editor's Notes

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