Scientific Programme & Abstracts from the International Meeting in Pediatric Endocrinology (IMPE)

impe0096ep61 | Pituitary, Neuroendocrinology and Puberty | IMPE2023

Adipsic Diabetes Insipidus (ADI) in A Pediatric Patient with Panhypopituitarism Secondary to Craniopharyngioma: A Rare Manifestation Potentially Fatal

Garcia Camila , Koller Osvaldo , Pablo Fernandez Jose , Isabel Hernandez Maria

Diabetes insipidus (DI) is characterized by polydipsia and polyuria with a dilute urine. Central DI (CDI) results from a deficiency of arginine vasopressin (AVP) and may be due to congenital or acquired causes, the latter include tumors affecting the hypothalamic-pituitary region. Thirst acts as a central biological backup mechanism in the absence of AVP, allowing plasma osmolarity to remain stable. We describe ADI patients with hypothalamic damage, who lose the ability to per...