Craniopharyngioma is a rare type of noncancerous (#benign) brain tumor.
#Craniopharyngioma begins near the brain’s pituitary gland, which secretes hormones that control many body functions. As a craniopharyngioma slowly grows, it can affect the function of the pituitary gland and other nearby structures in the brain.
Craniopharyngioma can occur at any age, but it occurs most often in #children and older adults. Symptoms include gradual changes in vision, fatigue, excessive urination and headaches. Children with craniopharyngioma may grow slowly and may be smaller than expected.
Tests and procedures used to diagnose craniopharyngioma include:
- #Physical_exam. Diagnosing a
craniopharyngioma usually starts with a
medical history review and a neurological
exam by your doctor. During this procedure,
your vision, hearing, balance, coordination,
reflexes, and growth and development are
tested.
- #Blood_tests. Blood tests may reveal
changes
in hormone levels that indicate a tumor is
affecting your pituitary gland.
- #Imaging_tests. Tests to create images of
your brain may include X-rays, magnetic
resonance imaging (MRI) and computerized
tomography (CT).
Craniopharyngioma treatment options include:
-
Surgery
-
Radiation Therapy
-
Chemotherapy
-
Treatment of Papillary Craniophyrangioma