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IMAGING DEPARTMENT
Jan 24th
, 2012
Reported by Dr. Le Giang
 Name: Doan Thi Tuyet Nhung
 Sex: Female
 Age: 4 y
 Dept: Outpatient
Clinical
 Visual disturbance
 Headache
MRI findings
T2WI, Axial
 Suprasellar & intrasellar mass (22x24x34 mm)
 Mixed component: cystic & solid part (calcification)
 Displacement of chiasm
MRI findings
T1WI, Sagital
 Sellar enlargement ( AP: 21mm) , hardly compress pituitary
 Heterogenous intensity (iso & hypo signal) calcification & fluid
 Cystic contents hyperintense to cerebrospinal fluid
MRI findings
T1WI, Coronal
 Cyst content hyperintense to CSF
MRI findings
T1WI, Axial, Post C+
 Solid portion enhance heterogenously
 Cyst wall strong enhances
 Circle of Willis encased by mass
MRI findings
T1WI, Post C+
 Compress hardly pituitary
MRI findings
T1WI, Post C+
 Solid portion enhance heterogenously
 Cyst wall strong enhances
Diagnosis
CRANIOPHARYNGIOMA
Background
 CrP is slow- growing & benign tumor.
 Histologically benign epithelial tumor arising from squamous rests along
involuted hypophyseal-Rathke duct.
 2 Types: Adamentinomatous & Papillary
 6-9% of all Ped intracranial tumors.
 Location: Suprasellar (75%), Supra & intrasellar ( 21%), Intrasellar (4%).
 Age: Peak at 8-12 y.
 Imaging findings: Cystic supracellar mass with calcification & enhancement
of a mural nodule of cyst wall. Displacement of chiasm.
 90% are cystic; 90% have calcification; 90% enhancement cyst wall
 Treatment: surgical & radiation therapy.
 Prognosis: 64-96% overall 10 years survival
20% recurrence rate if <5cm
80% recurrence rate if> 5cm
Can recur up to 30 years after resection.
Thank you for attention!

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Craniopharyngioma

  • 1. IMAGING DEPARTMENT Jan 24th , 2012 Reported by Dr. Le Giang
  • 2.  Name: Doan Thi Tuyet Nhung  Sex: Female  Age: 4 y  Dept: Outpatient
  • 4. MRI findings T2WI, Axial  Suprasellar & intrasellar mass (22x24x34 mm)  Mixed component: cystic & solid part (calcification)  Displacement of chiasm
  • 5. MRI findings T1WI, Sagital  Sellar enlargement ( AP: 21mm) , hardly compress pituitary  Heterogenous intensity (iso & hypo signal) calcification & fluid  Cystic contents hyperintense to cerebrospinal fluid
  • 6. MRI findings T1WI, Coronal  Cyst content hyperintense to CSF
  • 7. MRI findings T1WI, Axial, Post C+  Solid portion enhance heterogenously  Cyst wall strong enhances  Circle of Willis encased by mass
  • 8. MRI findings T1WI, Post C+  Compress hardly pituitary
  • 9. MRI findings T1WI, Post C+  Solid portion enhance heterogenously  Cyst wall strong enhances
  • 11. Background  CrP is slow- growing & benign tumor.  Histologically benign epithelial tumor arising from squamous rests along involuted hypophyseal-Rathke duct.  2 Types: Adamentinomatous & Papillary  6-9% of all Ped intracranial tumors.  Location: Suprasellar (75%), Supra & intrasellar ( 21%), Intrasellar (4%).  Age: Peak at 8-12 y.  Imaging findings: Cystic supracellar mass with calcification & enhancement of a mural nodule of cyst wall. Displacement of chiasm.  90% are cystic; 90% have calcification; 90% enhancement cyst wall  Treatment: surgical & radiation therapy.  Prognosis: 64-96% overall 10 years survival 20% recurrence rate if <5cm 80% recurrence rate if> 5cm Can recur up to 30 years after resection.
  • 12. Thank you for attention!