Craniopharyngioma

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  • Uncommon, benign (WHO I) tumor that occurs in both children & adults.

Subtypes of craniopharyngioma

Adamantinomatous craniopharyngioma

  • epithelium that form stellate reticulum, wet keratin & basal palisades.
  • Up to 95% of this variant shows CTNNB1 mutations & aberrant nuclear expression of β-catenin.
  • Bimodal age distribution: childhood peak age 5–15 yrs, adult peak age 45–60 years.

Papillary craniopharyngioma

  • epithelium that form papillary features.
  • MC in supratentorial compartment or 3rd ventricle.
  • 81–95% of cases show BRAF V600E mutations.
  • Usually solid, or rarely cystic.
  • almost exclusively in adults w/ ~40–55 y/o.

Overview of Adult and Pediatric Craniopharyngioma

Adult Pediatric
EPIDEMIOLOGY
Age in years 65–74 5–14
Gender M = F M > F
Clinical presentation Vision loss, hydrocephalus Headaches, hydrocephalus
Endocrine dysfunction Less common Common
RADIOLOGY
Cysts Less common Common
Calcification Less common Common
PATHOLOGY TYPE
Adamantinomatous Yes Yes
Papillary Yes No
TREATMENT OPTIONS
Surgery Yes Yes
Radiotherapy Yes Yes
Targeted therapy Yes (papillary subtype) No
TREATMENT MORBIDITY
Surgery Better tolerated than radiation
Radiotherapy Better tolerated than surgery