ABSTRACT
The pathogenesis, diagnosis, and management of adrenal tumors have recently evolved1,2 mainly because of easier discovery of clinically silent, incidentally detected adrenal tumors using more sensitive imaging procedures such as computed tomography (CT) and magnetic resonance imaging (MRI).3 Even if these tumors are rarely seen in children, it is important that the physician recognizes the clinical manifestations of these tumors as soon as possible, leading to an earlier diagnosis, prompt intervention, and improved survival.
