Adrenocortical carcinoma (ACC) is a rare endocrine malignancy, often with an unfavorable
prognosis. Here we summarize the knowledge about diagnosis, epidemiology …

This is a consensus statement from an international group, mostly of clinical
endocrinologists. MEN1 and MEN2 are hereditary cancer syndromes. The commonest …

The better understanding of the biological behavior of multiple endocrine neoplasia type 1
(MEN1) organ manifestations and the increase in clinical experience warrant a revision of …

Clinically silent adrenal masses discovered by imaging studies performed for unrelated
reasons, ie adrenal incidentalomas, have become a rather common finding in clinical …

The past two decades have brought many important advances in our understanding of the
hereditary susceptibility to cancer. Approximately 5–10% of all cancers are inherited, the …

Adrenal carcinoma in children is associated with virilism and a less aggressive natural
history; in adults it presents as a mixed Cushing‐virilizing syndrome and has a virulent …

Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development
of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome,
characterized primarily by multiple tumors in the parathyroid glands, endocrine pancreas …

Multiple endocrine neoplasia type 1 (MEN1) consists of benign, and sometimes malignant,
tumors (often multiple in a tissue) of the parathyroids, enteropancreatic neuroendocrine …

In patients with multiple endocrine neoplasia type 1 (MEN1), the most common functional
pancreatic endocrine tumor (PET) syndrome is Zollinger-Ellison syndrome (ZES). ZES has …