hrp0097p1-538 | Multisystem Endocrine Disorders | ESPE2023
Mirra Giulia
, Deodati Annalisa
, Ubertini Graziamaria
, Elisa Amodeo Maria
, Antonietta De Ioris Maria
, Mastronuzzi Angela
, Cavallo Federica
, Grossi Armando
Background: The treatment of high-risk neuroblastoma still represents a clinical challenge in pediatric oncology. About 50% of children survive after a multimodal treatment based on conventional and high dose chemotherapy, surgery, radiotherapy, differentiating treatment and immunotherapy.Aim: To evaluate endocrine long-term sequels in a pediatric cohort with high-risk neuroblastoma.Patient...