ea0063p847 | Adrenal and Neuroendocrine Tumours 3 | ECE2019
Gulec Yazır Merve
, Cankurtaran Yılmaz
, Gonca Oruk Guzide
, Onder Pamuk Barış
, Arıkan Etit Demet
Introduction: Adrenocorticalcarcinoma (ACC) is a rare malignancy with an aggressive prognosis, an incidance of 12 cases/million/year. It is the cause of 0.2% of all cancer deaths. It is seen in the 4th and 5th decades in adults and mostly unilateral and sporadic. Herein, we present a case of sarcomatoid type ACC which is symptomatic with mass compression and hypertansive attacks.Case presentation: A-52-year-old male was referred to our endocrinolog...