MEN1 is an inherited disorder that causes tumors in the endocrine glands and the duodenum, the first part of the small intestine. MEN1 is rare, occurring in about one in 30, people. Endocrine glands release hormones into the bloodstream. Hormones are powerful chemicals that travel through the blood, controlling and instructing the functions of various organs.

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MEN1 is an inherited disorder that causes tumors in the endocrine glands and the duodenum, the first part of the small intestine. MEN1 is rare, occurring in about one in 30, people. Endocrine glands release hormones into the bloodstream. Hormones are powerful chemicals that travel through the blood, controlling and instructing the functions of various organs. In MEN1, the overactive glands may include the parathyroids, pancreas, or pituitary. In people with MEN1, multiple endocrine glands form tumors and become hormonally overactive, often at the same time.

The overactive glands may include the parathyroids, pancreas, or pituitary. Most people who develop overactivity of only one endocrine gland do not have MEN1. How does MEN1 affect the endocrine glands and the duodenum? The body normally has four parathyroid glands, which are located close to the thyroid gland in the front of the neck. The parathyroids release into the bloodstream a chemical called parathyroid hormone PTH , which helps maintain a normal supply of calcium in the blood, bones, and urine.

Hyperparathyroidism In MEN1, all four parathyroid glands tend to be overactive, causing hyperparathyroidism. The parathyroid glands form tumors that release too much PTH, leading to excess calcium in the blood. High blood calcium, known as hypercalcemia, can exist for many years before it is found by accident or through screening for MEN1. Unrecognized hypercalcemia can cause excess calcium to spill into the urine, leading to kidney stones or kidney damage.

Also, the bones may lose calcium and weaken. Nearly everyone who inherits a susceptibility to MEN1 will develop hyperparathyroidism by age 50, but the disorder can often be detected before age Hyperparathyroidism may cause no problems for many years, or it may cause tiredness, weakness, muscle or bone pain, constipation, indigestion, kidney stones, or thinning of bones.

Doctors must decide whether hyperparathyroidism in MEN1 is severe enough to need treatment, especially in a person who has no symptoms. The usual treatment is an operation to remove most or all of the parathyroid glands. One option is to remove the three largest glands and all but a small part of the fourth. Another is to remove all four glands and at the same time transplant a small part of one gland into the forearm.

By maintaining a portion of one gland, the parathyroid transplant continues to release PTH into the bloodstream to do its job. After parathyroid surgery, regular testing of blood calcium should continue because often the small piece of remaining parathyroid tissue grows larger and causes recurrent hyperparathyroidism. If the remaining piece is in the forearm and additional surgery is needed to remove more parathyroid tissue, the arm operation can be performed under local anesthesia.

Sometimes all four glands are completely removed to prevent recurrence or may be unintentionally removed during parathyroid surgery.

People whose parathyroid glands have been completely removed must take daily supplements of calcium and vitamin D or another related treatment to prevent hypocalcemia, or low blood calcium. The Pancreas and Duodenum Located behind the stomach, the pancreas has two major roles: to release digestive juices into the intestines and key hormones into the bloodstream. The duodenum is the first part of the small intestine next to the pancreas. The pancreatic hormones are normally produced by small clusters of specialized cells called pancreatic islets.

Some of the major hormones produced by the pancreatic islets are insulin-lowers blood glucose, also called blood sugar glucagon-raises blood glucose somatostatin-inhibits secretion of certain other hormones vasoactive intestinal peptide VIP -causes intestinal cells to secrete water into the intestine gastrin-causes the stomach to produce acid for digestion Gastrinomas In MEN1, gastrin may be oversecreted by tumors called gastrinomas in the pancreas, duodenum, and lymph glands.

If exposed to too much gastrin, the stomach releases excess acid, leading to the formation of severe ulcers in the stomach and small intestine.

In addition, too much gastrin usually causes serious diarrhea. People with MEN1 have about a 20 to 60 percent chance of developing gastrinomas. The ulcers caused by untreated gastrinomas are much more dangerous than typical stomach or intestinal ulcers. Left untreated, they can cause rupture of the stomach or intestine and even death. The gastrinomas associated with MEN1 are not easily cured through tumor surgery because finding the many small gastrinomas in the pancreas, duodenum, and lymph glands is difficult.

The mainstay of treatment is powerful medicines called acid pump inhibitors that block stomach acid release.

Taken by mouth, these medicines have proven effective in controlling the complications of excess gastrin in most cases of Zollinger-Ellison syndrome. Rare Pancreatic Complications Occasionally, a person who has MEN1 develops an islet tumor of the pancreas that secretes high levels of hormones.

Insulinomas, for example, produce too much insulin, causing hypoglycemia, or low blood glucose. About 10 percent of adults with MEN1 develop insulinomas. Tumors that secrete adrenocorticotropin ACTH may also arise in the pancreas. ACTH is normally secreted by the pituitary gland and stimulates the adrenal glands to produce cortisol, a hormone that helps the body respond to stress. Tumors in the pancreas may also infrequently secrete gonadotropin-releasing hormone GnRH.

GnRH is normally secreted by the hypothalamus and stimulates the pituitary gland to release follicle stimulating hormone FSH , which regulates fertility in men through sperm production and in women through ovulation. In general, surgery is the mainstay of treatment for these uncommon types of tumors. The Pituitary Gland The pituitary, a small gland located at the base of the brain, produces many important hormones that regulate basic body functions.

The normal major pituitary hormones are prolactin-controls the formation of breast milk and influences fertility and bone strength growth hormone-regulates body growth, especially during adolescence ACTH-stimulates the adrenal glands to produce cortisol thyrotropin-stimulates the thyroid gland to produce thyroid hormones, which regulate metabolism luteinizing hormone-stimulates the ovaries or testes to produce sex hormones FSH-regulates fertility Prolactinomas The pituitary gland becomes overactive in about one in four people with MEN1.

High prolactin levels can cause excessive production of breast milk or interfere with fertility in women or with sex drive and fertility in men. Treatment may not be needed for prolactinomas. If treatment is needed, a medicine known as a dopamine agonist can effectively shrink the tumor and lower the production of prolactin.

Occasionally, prolactinomas do not respond well to this medication. In such cases, surgery, radiation, or both may be needed. Too much cortisol can lead to muscle weakness, weakened bones and fractures, and thinning skin, among other problems. Pituitary tumors that produce growth hormone cause excessive bone growth or disfigurement.

Are the tumors associated with MEN1 cancerous? The tumors associated with MEN1 are usually benign, meaning they are not cancerous. However, they can disrupt normal function by releasing hormones or by crowding nearby tissue. For example, a prolactinoma may become quite large in someone with MEN1. As it grows, the tumor can press against and damage the normal part of the pituitary gland or the nerves for vision. Sometimes impaired vision is the first sign of a pituitary tumor in a person with MEN1.

Another type of benign tumor seen in about one-third of people with MEN1 is a plum-sized, fatty tumor called a lipoma, which grows under the skin. Lipomas cause no health problems and can be removed by simple cosmetic surgery if desired.

Benign tumors do not spread to or invade other parts of the body. Cancer cells, by contrast, break away from the primary tumor and spread, or metastasize, to other parts of the body through the bloodstream or lymphatic system.

The pancreatic islet tumors associated with MEN1 tend to be numerous and small, but most are benign and do not release active hormones into the blood. Over time, gastrinomas may become cancerous but are usually slow-growing.

Eventually, about half of people with MEN1 will develop a cancerous pancreatic or carcinoid tumor. A carcinoid is a slow-growing endocrine tumor inside the chest or stomach of a person with MEN1.

Although carcinoids arise from endocrine cells, which are present in many parts of the body, they rarely secrete a hormone in a person with MEN1. Carcinoids of the stomach usually do not require treatment. Treatment of Pancreatic Endocrine Cancer in MEN1 Because the type of pancreatic endocrine cancer associated with MEN1 can be difficult to recognize, difficult to treat, and slow to progress, doctors have different views about the value of surgery in managing these tumors.

One approach is to "watch and wait," using medical, or nonsurgical, treatments. According to this school of thought, pancreatic surgery has serious complications, so it should not be attempted unless it will cure a tumor or cure a hormone excess state. Another school advocates early surgery, perhaps when a tumor grows to a certain size, to prevent or treat pancreatic endocrine cancer—even if the tumor does not over secrete a hormone-before the cancer spreads.

No clear evidence exists, however, that surgery to prevent pancreatic endocrine cancer from spreading actually leads to longer survival for patients with MEN1. Doctors agree that excessive release of certain hormones-mainly gastrin-from pancreatic endocrine cancer in MEN1 needs to be treated, and medications are often effective in blocking the effects of these hormones.

Some tumors, such as insulinomas, are usually benign and single and are curable by pancreatic surgery. Is MEN1 the same in everyone? Not only do the tumors of MEN1 vary among members of the same family, but some families with MEN1 tend to have a higher rate of prolactin-secreting pituitary tumors and a much lower frequency of gastrin-secreting tumors. The age at which MEN1 can begin to cause endocrine gland overactivity can differ strikingly from one family member to another.

One person may have only mild hyperparathyroidism beginning at age 50, while a relative may develop complications from tumors of the parathyroid, pancreas, and pituitary by age How is MEN1 detected? MEN1 is detected by gene testing or, when gene testing is unavailable or yields a negative result, by laboratory tests that measure hormone levels.

Many different MEN1 gene mutations have been identified. Each of these mutations can cause the same spectrum of MEN1 tumors.

MEN1 is an autosomal dominant gene, which means it is inherited by a child from one parent who has the MEN1 mutation. Once identified, carriers undergo approximately yearly testing, a process called screening, for biochemical indications of a developing tumor. The gene tests are expensive and can be time-consuming. Once a specific mutation is found in an individual, the gene test for relatives is easier and less expensive.

In 10 to 30 percent of families with MEN1, no mutation is found. Less often, the person carries a new MEN1 gene mutation. Genetic counseling may include a review and discussion of the psychosocial benefits and risks of genetic testing. Genetic testing results can affect self-image, self-esteem, and individual and family identity.

In genetic counseling, issues related to how and with whom genetic test results will be shared and their possible effect on important matters such as health and life insurance coverage can be addressed. These discussions may occur when a family member is deciding whether to proceed with gene testing and again later when the test results are available.

A doctor, nurse, or genetics professional provides the genetic counseling. Screening can catch tumors in their early stages of development, detect tumors that have come back, and indicate how large they are and where they are located.


Multiple Endocrine Neoplasia Type 1

Although a variety of additional eponyms have been proposed for MEN2B e. Williams-Pollock syndrome, Gorlin-Vickers syndrome, and Wagenmann—Froboese syndrome , none ever gained sufficient traction to merit continued use and, indeed, are all but abandoned in the medical literature. Another early report was Schimke et al. The first exon and the last part of exon 10 are not translated. A main transcript of 2.


Neoplasia endocrina múltiple



Neoplasia endocrina múltiple (NEM) I


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