AACE released clinical guidelines on the diagnosis, management, and surveillance of tumors related to multiple endocrine neoplasia type 1.

Please note - this trial is no longer recruiting patients. We hope to add results when they are available. Neuroendocrine tumours (NET’s) are rare tumours that develop in the nerve or gland cells that ...

Localization and complete surgical removal of a gastrinoma should be attempted for cure in all patients unless widespread hepatic metastases exist. The presence of hepatic metastasis is probably ...

About 80% of patients with MEN-1 have a pancreatic tumor, the most common form of which is a gastrinoma (seen in 40%-50% of cases). An insulinoma occurs in about 20% of patients and, less commonly ...

ASCO Guidelines provide recommendations with comprehensive review and analyses of the relevant literature for each recommendation, following the guideline development process as outlined in the ASCO ...

Multiple endocrine neoplasia (MEN) is a group of rare genetic conditions that increase the risk of certain tumors in your glands. Parathyroid, thyroid, adrenal glands, and digestive tract tumors ...