Several different combinations of endocrine tumors are known to occur together, and each of these patterns is categorized as one of several different MEN syndromes.
Multiple endocrine neoplasia syndromes can affect these major endocrine glands:
AdrenalPancreasParathyroidPituitaryThyroid
The tumors that develop as part of each MEN syndrome may be benign or malignant. Benign tumors are abnormal tumors that can cause medical symptoms but grow slowly, do not spread to other parts of the body, and are not fatal.
Malignant tumors are cancerous tumors that can grow rapidly, may spread to other parts of the body, and can be fatal if they are left untreated.
Cause
Each of the three syndromes that are considered the most common manifestations of MEN is caused by a specific genetic abnormality, and the tumor combination often runs in families as a hereditary condition.
This condition is inherited in an autosomal dominant pattern. About 50% of children of people with MEN syndromes will develop the disease and 50% won’t.
Furthermore, a person with a family history MEN cannot pass it on to their children unless they themselves have inherited the gene that causes MEN. In other words, if one of your parents has MEN, but you do not, your children have no risk of getting the disease.
Types and Symptoms
The MEN syndromes are called MEN 1, MEN 2A, and MEN 2B (which was formerly called type 3). Each has a unique set of symptoms to consider.
MEN 1
People diagnosed with MEN 1 have tumors of the pituitary gland, the parathyroid gland, or the pancreas. Generally, these tumors are benign, although it is not impossible for them to become malignant.
The symptoms of MEN 1 can begin during childhood or adulthood. The symptoms are variable because the tumors involve endocrine organs that can produce a wide range of effects on the body. Each of the tumors causes abnormal changes related to hormonal overactivity. Possible symptoms of MEN 1 include:
Difficulty breathing Headaches, high blood pressure, irregular heartbeat, and panic attacks Hyperparathyroidism, in which the parathyroid gland produces too much hormone, and can cause tiredness, weakness, muscle or bone pain, constipation, kidney stones, or thinning of bones. Hyperparathyroidism is usually the first sign of MEN1 and typically occurs between the ages of 20 and 25. Nearly everyone with MEN1 will develop hyperparathyroidism by the age of 50. Irregular periods in women; reduced sexual desire or erectile dysfunction in men Nausea, diarrhea, and vomiting
MEN 2A
People with MEN 2 have thyroid tumors, adrenal gland tumors, or parathyroid tumors. The symptoms of MEN 2A begin during adulthood, typically when a person is in their 30s. As with the other MEN syndromes, the symptoms result from overactivity of the endocrine tumors and include:
Chest painFrequent urge to urinateHeadachesHigh blood pressureRapid heartbeatSweating
MEN 2B
As the least common of these rare tumor patterns, MEN 2B is characterized by thyroid tumors, adrenal gland tumors, neuromas throughout the mouth and digestive system, abnormalities of bone structure, and an unusually tall and skinny stature with long fingers, toes, arms, and legs. Together, these features are known as marfanoid habitus.
Other symptoms can begin in childhood, often before age 10, and include:
Nerve pain Stomach and digestive problems Symptoms of thyroid cancer and pheochromocytoma (a rare and usually noncancerous tumor)
Diagnosis
Your healthcare provider may be concerned that you may have MEN syndrome if you have more than one endocrine tumor and your family history includes people with the syndrome. You do not need to have all of the signature tumors of one of the MEN syndromes for your healthcare provider to consider the disease. If you have more than one tumor or characteristic, or even if you have one endocrine tumor that is associated with MEN, your healthcare provider may evaluate you for other tumors before they become symptomatic.
A family history is not necessary for MEN diagnosis because a person can be the first in the family to have the disease. The specific genes that cause MEN have been identified, and genetic testing may be an option in confirming the diagnosis.
Diagnostic tests may include:
Blood tests Urine tests Imaging tests, which may include computed axial tomography (CT or CAT) scans or magnetic resonance imaging (MRI) scans
Treatment
The treatment for the MEN syndromes depends on several different factors. Not everyone who is diagnosed with MEN 1, MEN 2A, or MEN 2B experiences the same exact disease course. Generally, treatment is focused on three main objectives: reducing symptoms, detecting tumors early, and preventing the consequences of malignant tumors.
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If you are diagnosed with one of the MEN syndromes, your treatment will be customized to your particular needs. One or more of the following therapies may be recommended to treat the disease or help relieve symptoms.
Medications to help balance hormone levels or treat symptomsSurgical removal of the affected gland to treat symptoms (Hyperparathyroidism caused by MEN1 is typically treated with surgical removal of three-and-a-half of the four parathyroid glands, although sometimes all four glands are removed. )
Active surveillance and monitoring to identify new tumors and to spot any malignancy as early as possible may also be recommended.
Summary
Multiple endocrine neoplasia (MEN) is the name for a group of hereditary illnesses characterized by having more than one tumor of the endocrine organs at a time. MEN syndromes can affect the major endocrine glands: adrenal, pancreas, parathyroid, pituitary, and thyroid. The tumors that develop as part of each MEN syndrome may be benign or malignant. Symptoms vary, and the success of treatment often depends on how early the disease is detected.
A Word From Verywell
Finding out you have a tumor is distressing, and having more than one tumor is even more frightening. If you have been told that you have multiple endocrine neoplasia, then you are probably quite concerned about which symptoms could emerge next and whether your overall health is in danger.
The fact that MEN syndromes are recognized and classified makes your situation more predictable than it may seem. Despite the fact that these are rare syndromes, they have been defined in great detail. Plus, there are well-established methods for managing these illnesses. While you will certainly need consistent medical follow-up, there are effective ways to control the condition. And with prompt diagnosis and appropriate treatment, you can live a healthy life.
