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Information

Nervous System Disorders

Incidence: 3–4% of all intracranial neoplasms; 15% of supratentorial + 50% of suprasellar tumors in children; most common suprasellar mass

Origin: from epithelial rests along vestigial craniopharyngeal duct + primitive buccal epithelium (Rathke cleft cells within intermediate lobe of pituitary gland)

Path: cystic (rich in liquid cholesterol) / complex / solid

Age: from birth–7th decade; M >F; bimodal age distribution with age peaks in 1st–2nd decade (75%) and in 4th–6th decade (25%)

Location: anywhere along infundibular stalk from floor of 3rd ventricle to pituitary gland

  1. suprasellar (20%)
  2. intrasellar (10%)
  3. intra- and suprasellar (70%)
    Ectopic craniopharyngioma:
  4. floor of anterior 3rd ventricle (more common in adults)
  5. sphenoid bone

Skull films:

CT:

MR (relatively ineffective in demonstrating calcifications):

Angio:

DDx:

  1. Epidermoid (no contrast enhancement)
  2. Rathke cleft cyst (small intrasellar lesion)
  3. Hemorrhagic pituitary macroadenoma (fluid-fluid level)