Pituitary tumors are abnormal growths that develop in your pituitary gland. Some pituitary tumors cause excessive production of hormones that regulate important functions of your body. Other pituitary tumors can restrict normal functions of your pituitary gland, causing it to produce lower levels of hormones.

The vast majority of pituitary tumors are noncancerous growths (adenomas). Adenomas remain confined to your pituitary gland or surrounding tissues and doesn’t spread to the other parts of your body.

Treatment for pituitary tumors involves various options, including removing the tumor, controlling its growth and managing your hormone levels with medications.


The tumor can cause your pituitary gland to produce too much or too less hormones, which can cause problems. Large tumors — those measuring about 1 centimeter (slightly less than a half-inch) or more — are known as macroadenomas. Small tumors are called microadenomas. Macroadenomas can put pressure on the rest of the pituitary gland and surrounding structures.

Signs and symptoms of pressure from a pituitary tumor may include:

  • Headache
  • Vision loss, particularly loss of peripheral vision
  • Nausea and vomiting
  • Symptoms of pituitary hormone deficiency
  • Weakness
  • Less frequent or no menstrual periods
  • Body hair loss
  • Sexual dysfunction
  • Increased frequency and amount of urination
  • Unintended weight loss or gain

Symptoms related to hormone level changes

Some pituitary tumors, called functioning tumors, also produce hormones, generally causing an overproduction of hormones. Different types of functioning tumors can develop in your pituitary gland, each causing specific signs and symptoms and sometimes a combination of them.

Adrenocorticotropic hormone-secreting (ACTH) tumors

ACTH tumors produce the hormone adrenocorticotropin, which stimulates your adrenal glands to make the hormone cortisol. Cushing's syndrome results from your adrenal glands producing too much cortisol. Signs and symptoms of Cushing's syndrome may include:

  • Fat accumulation around your midsection and upper back
  • Exaggerated facial roundness
  • A characteristic hump on the upper part of your back
  • High blood pressure
  • High blood sugar
  • Muscle weakness
  • Bruising
  • Stretch marks
  • Thinning of your skin
  • Anxiety, irritability or depression

Growth hormone-secreting tumors

These tumors produce excess growth hormone. The effects from excess growth hormone (acromegaly) may include:

  • Coarse facial features
  • Enlarged hands and feet
  • Excess sweating
  • High blood sugar
  • Heart problems
  • Joint pain
  • Mal-aligned teeth
  • Increased growth of body hair

Accelerated and excessive linear growth may occur in children and adolescents.

Prolactin-secreting tumors

Overproduction of prolactin from a pituitary tumor (prolactinoma) can cause a decrease in normal levels of sex hormones — estrogen in women and testosterone in men. Excessive prolactin in the blood can affect men and women differently.

In women, prolactinoma may cause:

  • Irregular menstrual periods
  • Lack of menstrual periods
  • Milky discharge from the breasts

In men, a prolactin-producing tumor may cause male hypogonadism. Signs and symptoms may include:

  • Erectile dysfunction (ED)
  • Infertilituy
  • Loss of sex drive

Thyroid-stimulating hormone-secreting tumors

When a pituitary tumor overproduces thyroid-stimulating hormone, your thyroid gland makes too much of the hormone thyroxine. This is a rare cause of hyperthyroidism or overactive thyroid disease. Hyperthyroidism can accelerate your body's metabolism, causing:

  • Sudden weight loss
  • Rapid or irregular heartbeat
  • Nervousness or irritability
  • Frequent bowel movements
  • Feeling warm or hot

Pituitary tumors often can be treated effectively to return your hormone levels to normal and alleviate your signs and symptoms. If you know that multiple endocrine neoplasia, type I (MEN I) runs in your family, talk to your doctor about periodic tests that may help detect a pituitary tumor early.

Possible Cause

The cause of the pituitary gland tumor, remains unknown. The pituitary gland is a small, bean-shaped gland situated at the base of your brain, somewhat behind your nose and between your ears. Despite its small size, the gland influences nearly every part of your body. The hormones it produces help regulate important functions, such as growth, blood pressure and reproduction.

A small percentage of pituitary tumor cases runs in families, but most have no apparent hereditary factor. Still, scientists suspect that genetic alterations play an important role in how it develops.

Risk Factors

Although pituitary tumors can occur at any age, they're most likely to occur in older adults. People with a family history of certain hereditary conditions, such as multiple endocrine neoplasia, type I (MEN I), have an increased risk of pituitary tumors. In MEN I, multiple tumors occur in various glands of the endocrine system. Genetic testing is available for this disorder.


Pituitary tumors usually don't grow or spread extensively. However, they can adversely affect your health, possibly causing:

  • Vision loss A pituitary tumor can put pressure on the optic nerves, which are close to your pituitary gland, and cause loss of vision.
  • Permanent hormone deficiency The presence of a pituitary tumor or the removal of one may permanently alter your hormone supply, which may need to be replaced with hormone medications.
  • Diabetes insipidus This is a possible complication of a large pituitary tumor or of some treatments for pituitary tumors. Not to be confused with the more common diabetes mellitus, which involves high sugar levels in the blood and urine, diabetes insipidus is the result of the pituitary making too little vasopressin, which controls the concentration of urine in the kidneys. Diabetes insipidus causes excess amounts of urine and severe thirst, which can lead to dehydration. A rare but potentially serious complication of a pituitary tumor is pituitary apoplexy, when sudden bleeding into the tumor occurs. Pituitary apoplexy requires emergency treatment, usually with corticosteroids and possibly surgery.



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