A craniopharyngioma is a rare, noncancerous (benign) brain tumor that usually develops near the pituitary gland and the hypothalamus. Although slow-growing, its location near critical structures can cause significant hormonal, vision, and neurological issues.

What Is Craniopharyngioma?

Craniopharyngiomas arise from embryonic remnants of Rathke's pouch along the pathway of the pituitary gland. They are technically benign (WHO grade 1) but behave aggressively locally, often compressing the optic nerves, pituitary stalk, and hypothalamus. They typically contain fluid-filled cysts and calcifications.

At a Glance

  • Rare, benign tumors developing near the pituitary gland
  • Bimodal age distribution: peaks in childhood (5-14 years) and adulthood (50-74 years)
  • Commonly causes visual field deficits and hormonal imbalances
  • Maximal safe surgical resection is the primary treatment
  • Often requires multidisciplinary care including neurosurgery, endocrinology and neuro-ophthalmology

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