ea0056p117 | Endocrine tumours and neoplasia | ECE2018
Kostiainen Iiro
, Hakaste Liisa
, Kejo Pekka
, Parviainen Helka
, Laine Tiina
, Pennanen Mirkka
, Arola Johanna
, Haglund Caj
, Heiskanen Ilkka
, Schalin-Jantti Camilla
Background: Adrenal cortical carcinoma (ACC) is a rare malignancy known to be highly aggressive, with few specific treatment options. The objective was to evaluate clinicopathological features and outcome in patients treated at Helsinki University HospitalMethods and patients: We included all patients diagnosed with adrenocortical carcinoma (Weiss score ≥4) at Helsinki University Hospital during the years 2002 through 2017. Patients were identified...