Multiple Endocrine Neoplasia Type 2
Also known as: MEN2, MEN 2A syndrome, MEN 2B syndrome.
What is multiple endocrine neoplasia type 2?
Multiple endocrine neoplasia type 2 is a disease that affects several glands throughout the body, including the thyroid, parathyroid and adrenal gland. It causes tumors in these glands and also imbalances in the hormones that the glands produce. It differs from multiple endocrine neoplasia type 1 based on the genetic mutation that causes it, and some of the glands that it impacts.
What causes multiple endocrine neoplasia type 2?
Multiple endocrine neoplasia type 2 is the result of a genetic mutation. The disease is passed down from parents to children.
What are the symptoms of multiple endocrine neoplasia type 2?
The tumors that are typical of multiple endocrine neoplasia type 2 lead to hormone imbalances, which in turn produce symptoms such as kidney stones, bone loss, bone pain, constipation, indigestion, fatigue and other symptoms. Though the tumors are usually benign, they can increase the risk of cancer developing over time.
What are multiple endocrine neoplasia type 2 care options?
Surgery to remove the tumor is often the recommended treatment for multiple endocrine neoplasia type 2. Medications can also help with many of the symptoms related to the disease.
Close follow up and monitoring with blood tests and ultrasound and MRI is essential to detect any tumor at an early stage.
Reviewed by: Ziad A Khatib, MD
This page was last updated on: June 21, 2019 02:25 AM
Date: Saturday, July 25, 2020
Camp U.O.T.S. is an annual weeklong, overnight camp for children with cancer and blood disorders who are treated at Nicklaus Children’s Hospital.
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This event has been postponed. Please join us for an intimate conversation on personalized medicine and preconception screening, with special speakers Vladi Yurovsky, Daria Salyakina, Phd, and Debbie Wasserman, MS. Come get screened for Jewish genetic diseases!