hrp0089p2-p324 | Pituitary, Neuroendocrinology and Puberty P2 | ESPE2018
, Sette Giulia
, Cianfarani Stefano
, Cappa Marco
Craniopharyngioma is a rare, embryonic malformation of the sellar/parasellar region with low histological grade. In childhood-onset craniopharyngioma (CoCR), endocrine dysfunctions, severe obesity and metabolic syndrome (MetS), neurological impairment and reduced quality of life have been described as consequences of both localization and treatment. To characterize a population with CoCR and to correlate endocrine/metabolic sequelae with different surgery approach we performed...