ea0056p119 | Endocrine tumours and neoplasia | ECE2018
Simo-Servat Andreu
, Alonso Sara
, Guerrero Fernando
, Garcia-Sancho Paurla
, Marengo Agustina P.
, Iglesias Pedro
, Jose Diez Juan
, Peiro Inma
, Villabona Carles
Background: Adrenocortical carcinoma (ACC) is a rare and aggressive neoplasm with a 5-year survival rate <30%. Survival depends mainly on the stage at diagnosis, being surgery the only curative treatment.Objective: To report the clinical features, management and outcomes of a series of ACC in two Spanish tertiary hospitals.Material and methods: All patients with pathological diagnosis of ACC between 2000 and 2017 were included ...