The symptoms of a craniopharyngioma are.
Headache.
Peripheral field vision loss.
Eye movement weakness/double vision.
Vomiting.
Personality changes, confusion.
Hormonal insufficiency/hypothalamic dysfunction.
Adrenal insufficiency.
Craniopharyngioma is a rare brain tumor which usually form near the pituitary gland and the hypothalamus.
The Craniopharyngiomas are benign (not cancer) and do not spread to other parts of the brain or to other parts of the body.
The symptoms of craniopharyngiomas are.
Headache.
Peripheral field vision loss.
Eye movement weakness/double vision.
Vomiting.
Personality changes, confusion.
Hormonal insufficiency/hypothalamic dysfunction.
Adrenal insufficiency.
Although because of their aggressive local growth and location near delicate structures in the brain, craniopharyngiomas can cause devastating neurological symptoms.
And their propensity to attach to vital glands, brain structures, and blood vessels makes it difficult to remove entire tumors with surgery.
Craniopharyngiomas are most commonly found in children between the ages of 5 and 14.
However, adults over age 50 can also develop these tumors.
Following treatment, patients diagnosed with a craniopharyngioma have 10-year survival rates of approximately 90%.
This means that 90% of patients live at least 10 years.
Apart from those deaths directly attributed to the tumor and those related to the surgical interventions, the risk of cardio-/cerebrovascular and respiratory mortality is increased.