History and exam

Key diagnostic factors

common

visual loss

Due to anterior optic tract compression or tumor infiltration.[4][6][24] Children are more likely to present with acute loss of vision; in other age groups visual loss, although common, may be insidious in onset.

macrocephaly and hydrocephalus

Macrocephaly may be seen in infants before intracranial sutures fuse, and suggests hydrocephalus, secondary to ventricular outflow obstruction by an intracranial mass.[3][4]

growth failure

Craniopharyngioma is the most common cause of growth failure due to an intracranial tumor.[4][8][14]

In children with craniopharyngioma, growth hormone deficiency (causing growth failure) commonly precedes diagnosis.[25] Growth failure is rarely a cause for referral prior to diagnosis of craniopharyngioma.[8][26]

Other diagnostic factors

common

symptoms of hypogonadotropic hypogonadism (amenorrhea, erectile dysfunction)

Craniopharyngioma may present with common symptoms of endocrine dysfunction in older patients.[4][8][9][10][14]

Symptoms of hypogonadism in women include primary or secondary amenorrhea and, in men, erectile dysfunction due to low testosterone secondary to compression of the adenohypophysis or to elevated prolactin.

headache

Brain tumors often cause headaches that are progressive, often associated with other neurologic symptoms, and may be worse in the morning.[2][3][4]

symptoms of intracranial hypertension (nausea, vomiting, decreased sensorium, diplopia)

Raised intracranial pressure is seen with large craniopharyngiomas. Develops as a consequence of tumor obstructing the aqueduct or foramina of Monro, resulting in hydrocephalus.[2][3][4]

May develop acutely.

galactorrhea

Result of hyperprolactinemia secondary to compression of the adenohypophysis, the pituitary stalk, or hypothalamus.[4][8][9][14]

uncommon

optic atrophy

Due to chronic optic nerve compression by tumor or chronic intracranial hypertension.[2][3][4]

polyuria/polydipsia

Result of diabetes insipidus with decreased vasopressin release secondary to pituitary stalk or hypothalamic compression by tumor.[4][8][9][14]

Risk factors

weak

age 5 to 14 years

Although craniopharyngioma may present at any age, a bimodal age distribution is reported with a peak between 5 and 14 years of age and between 50 and 70 years of age.[12][15][16][17]

age 50 to 70 years

Although craniopharyngioma may present at any age, a bimodal age distribution is reported with a peak between 5 and 14 years of age and between 50 and 70 years of age.[12][15][16][17]

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