Adrenocortical carcinoma (ACC) is an uncommon aggressive endocrine malignancy that is
nonetheless associated with significant mortality and morbidity rates because of endocrine …

Adrenocortical carcinoma (ACC) is a heterogenous group of diseases with different clinical
behaviour between adult and paediatric patients. In addition, three histological variants …

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy arising from the adrenal
cortex often with unexpected biological behavior. It can occur at any age, with two peaks of …

Introduction: Adrenocortical carcinoma (ACC) is a rare tumor, often discovered at an
advanced stage and associated with poor prognosis. Treatment is guided by staging …

Context Prognosis of metastatic pheochromocytoma/paraganglioma following 131-Iodine
metaiodobenzylguanidine (MIBG) is incompletely characterized due to small samples and …

The adrenal gland is home to an array of complex physiological and neoplastic disease
processes. While dedicated adrenal computed tomography (CT) is the gold standard …

Gap junctions (GJs) are important in the regulation of cell growth, morphology, differentiation
and migration. However, recently, more attention has been paid to their role in the …

Objective To analyze the clinical and analytical features, diagnostic tests, therapies, and
outcomes of pheochromocytoma (PCC). Design and Methods A multicenter retrospective …

Background Adrenal tumours are associated with familial adenomatous polyposis (FAP). In
the literature, most studies use the clinical definition of FAP (more than 100 adenomatous …

Purpose The literature assessing outcomes of partial adrenalectomy (PA) among patients
with pheochromocytoma patients is largely limited to isolated, single-institution series. We …