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Pediatr Blood Cancer ; 70(11): e28493, 2023 11.
Artículo en Inglés | MEDLINE | ID: mdl-32790146

RESUMEN

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.


Asunto(s)
Craneofaringioma , Hipopituitarismo , Neoplasias Hipofisarias , Niño , Humanos , Craneofaringioma/terapia , Renta , Gestión de Riesgos , Neoplasias Hipofisarias/terapia
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