Craniopharyngioma

Therapeutic area
Neurology
Rare disease
Yes

Definition
A benign, partly cystic, epithelial tumor of the sellar region, presumably derived from Rathke pouch epithelium. It affects mainly children and young adults. There are two clinicopathological forms: adamantinomatous craniopharyngioma and papillary craniopharyngioma. The most significant factor associated with recurrence is the extent of surgical resection, with lesions greater than 5 cm in diameter carrying a markedly worse prognosis. (Adapted from WHO)
Genetic basis
No
Non-human condition
No
Rare disease
Yes
Listing at source
Listed
Condition name
Craniopharyngioma
Therapeutic area
Neurology

  • craniopharyngioma
  • Rathke pouch neoplasm
  • Rathke pouch tumor
  • Rathke pouch tumour
  • Rathke's pouch neoplasm
  • Rathke's pouch tumor
  • Rathke's pouch tumour
  • craniopharyngioma (WHO grade I)
  • craniopharyngioma (morphologic abnormality)
  • craniopharyngioma, benign
  • neoplasm of Rathke's pouch
  • tumor of Rathke's pouch
  • tumour of Rathke's pouch
  • Adamantinomatous tumor
  • Adamantinomatous tumour
  • Dysodontogenic epithelial tumor
  • Dysodontogenic epithelial tumour
  • craniopharyngeal duct tumor
  • craniopharyngeal duct tumour

Severity
Mild

  • Neurology
  • Oncology
  • Rheumatology

MONDO ID
Parent condition
MONDO:0000628

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Trials (71)

Drugs in development (9)

Other linked drugs (1)