“…Adrenocortical carcinoma (ACC) is an uncommon, aggressive malignant tumor with an incidence of 0.5-2.0 cases per million inhabitants per year [1][2][3]. ACC has a bimodal age distribution, with small peaks in the first decades and a larger peak in the fourth to fifth decades of life [2,3]. Patients with functional ACC may present with excess steroid hormone production resulting in Cushing syndrome with or without virilization [2,3], while non-functional ACC patients may present with either symptoms related to tumor mass, such as abdominal discomfort, nausea, vomiting, and back pain, or discovered incidentally during radiological procedures [2,3].…”