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Hypopituitarism is a condition in which the pituitary gland does not produce normal amounts of some or all of its hormones.
The pituitary gland is a small structure that is located just below the brain. It is attached by a stalk to the hypothalamus, the area of the brain that controls its function.
The hormones released by the pituitary gland (and their functions) are:
- Adrenocorticotropic hormone (ACTH) -- stimulates the adrenal gland to release cortisol; cortisol helps to maintain blood pressure and blood sugar
- Antidiuretic hormone (ADH) -- controls water loss by the kidneys
- Follicle stimulating hormone (FSH) -- controls sexual function and fertility in males and females
- Growth hormone (GH) -- stimulates growth of tissues and bone
- Luteinizing hormone (LH) -- controls sexual function and fertility in males and females
- Oxytocin -- stimulates the uterus to contract during labor and the breasts to release milk
- Prolactin -- stimulates female breast development and milk production
- Thyroid stimulating hormone (TSH) -- stimulates the thyroid gland to release hormones that affect the body's metabolism
In hypopituitarism, there is a lack of one or more pituitary hormones. Lack of the hormone leads to loss of function in the gland or organ that it controls. For example, no TSH leads to loss of function in the thyroid gland.
Hypopituitarism may be caused by:
- Brain surgery
- Brain tumor
- Head trauma
- Infections of the brain and the tissues that support the brain
- Subarachnoid hemorrhage (from a burst aneurysm)
- Tumors of the pituitary gland or hypothalamus
Occasionally, hypopituitarism is due to uncommon immune system or metabolic diseases, such as:
Hypopituitarism is also a rare complication after pregnancy, a condition called Sheehan's syndrome.
- Abdominal pain
- Decreased appetite
- Decreased sexual interest (in men)
- Failure to release milk (in women)
- Infertility (in women)
- Lack of sex drive (in women)
- Loss of armpit or pubic hair
- Loss of body or facial hair (in men)
- Low blood pressure
- Sensitivity to cold
- Short height (less than 5 feet) if onset is during a growth period
- Slowed growth and sexual development (in children)
- Stopping of menstrual periods (in women)
- Vision problems
- Weight loss
Note: Symptoms may develop slowly and may vary greatly, depending upon:
- The number of hormones that are missing and the organs they affect
- The severity of the disorder
Other symptoms that may occur with this disease:
Exams and Tests
To diagnose hypopituitarism, there must be low hormone levels due to a problem with the pituitary gland. The diagnosis must also rule out diseases of the organ that is affected by this hormone.
- Brain CT scan
- Pituitary MRI
- Serum ACTH
- Serum cortisol
- Serum estradiol (estrogen)
- Serum follicle stimulating hormone (FSH)
- Serum insulin-like growth factor 1 (IGF-1)
- Serum luteinizing hormone (LH)
- Serum testosterone level
- Serum thyroid stimulating hormone (TSH)
- Thyroid hormone (T4)
Levels of a pituitary hormone may be high in the bloodstream if you have a pituitary tumor that is producing too much of that hormone. The tumor may crush other cells of the pituitary, leading to low levels of other hormones.
If hypopituitarism is caused by a tumor, you may need surgery to remove the tumor, with or without radiation therapy.
You will need lifelong hormone therapy to replace hormones that are no longer made by organs under the control of the pituitary gland. These may include:
- Corticosteroids (cortisol)
- Growth hormone
- Sex hormones (testosterone for men and estrogen for women)
- Thyroid hormone
Drugs are also available to treat related infertility in men and women.
Hypopituitarism is usually permanent and requires lifelong treatment. However, you can expect a normal life span.
Side effects of drug therapy can develop. In severe illness, failing to take extra corticosteroids can be life-threatening.
When to Contact a Medical Professional
Call your health care provider if you develop symptoms of hypopituitarism.
In most cases, the disorder is not preventable. Awareness of risk may allow early diagnosis and treatment.
Melmed S, Kleinberg D, Ho K. Pituitary physiology and diagnostic evaluation. In: Kronenberg H, Melmed S, Polonsky KS, Larsen PR, eds. Williams Textbook of Endocrinology. 12th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 8.
Reviewed By: Nancy J. Rennert, MD, Chief of Endocrinology & Diabetes, Norwalk Hospital, Associate Clinical Professor of Medicine, Yale University School of Medicine, New Haven, CT. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.