Multiple endocrine neoplasia type 1 (patient information)
Jump to navigation Jump to search
Multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 1 On the Web
- Multiple endocrine neoplasia (MEN) type I is a disease passed down through families, in which one or more of the endocrine glands are overactive or form a tumor. Endocrine glands most commonly involved include pancreas, parathyroid and pituitary.
What are the symptoms of multiple endocrine neoplasia type 1?
- Visual disturbance
What causes multiple endocrine neoplasia type 1?
- MEN1 is an inherited disorder that causes tumors in the endocrine glands and the duodenum, the first part of the small intestine. Genetic mutations is speculated to be the cause of the disease.
Who is at highest risk?
- Age <40 years
- Positive family history
- Multifocal or recurrent neoplasia
- Two or more organ systems tumor involvement
- MEN1 is detected by gene testing or, when gene testing is unavailable or yields a negative result, by laboratory tests that measure hormone levels. Less often, MEN1 is diagnosed based on an individual's medical and family history.
When to seek urgent medical care?
- Seek urgent medical care if there are symptoms of MEN 1 or its complications.
- MEN1 cannot be cured, but regular testing can detect the problems caused by MEN1 tumors many years before serious complications develop.
- Surgery is indicated for pancreatic tumors.
Where to find medical care for multiple endocrine neoplasia type 1?
What to expect (Outlook/Prognosis)?
- Most people with MEN1 have a long and productive life.
- Most of the tumors are benign while some pancreatic tumors may become cancerous and lower life expectancy.