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Pediatr Blood Cancer ; 70(11): e28493, 2023 11.
Article in English | MEDLINE | ID: mdl-32790146

ABSTRACT

Pediatric craniopharyngioma is a rare tumor with excellent survival but significant long-term morbidities due to the loco-regional tumor growth or secondary to its treatment. Visual impairment, panhypopituitarism, hypothalamic damage, and behavioral changes are among the main challenges. This tumor should be managed under the care of a multidisciplinary team to determine the optimum treatment within the available resources. This is particularly important for low middle-income countries where resources are variable. This report provides risk-stratified management guidelines for children diagnosed with craniopharyngioma in a resource-limited setting.


Subject(s)
Craniopharyngioma , Hypopituitarism , Pituitary Neoplasms , Child , Humans , Craniopharyngioma/therapy , Income , Risk Management , Pituitary Neoplasms/therapy
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