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Hypopituitarism is a medical condition in which the pituitary gland does not produce enough hormones. The pituitary gland is a small gland located at the base of the brain that produces hormones that control various bodily functions.
Hypopituitarism can be caused by damage to the pituitary gland from surgery, radiation therapy, traumatic brain injury, or certain infections. Genetic factors can also play a role. Symptoms of hypopituitarism can vary depending on which hormones are affected but may include fatigue, weight gain, low blood pressure, and sexual dysfunction.
Treatment for hypopituitarism may involve hormone replacement therapy to help restore normal hormone levels. This may include medications to replace thyroid hormones, cortisol, and sex hormones. In some cases, growth hormone replacement therapy may also be necessary to help promote normal growth and development.
It is important for people with hypopituitarism to work closely with their healthcare provider to manage the condition and prevent complications. If left untreated or poorly managed, hypopituitarism can lead to serious complications, including adrenal crisis, diabetes insipidus, and growth and developmental delays.
If you or someone you know is experiencing symptoms of hypopituitarism, it is important to speak with a healthcare provider for an accurate diagnosis and appropriate treatment.
Hypopituitarism has a number of causes. In many cases, hypopituitarism is caused by a tumor of the pituitary gland. As a pituitary tumor increases in size, it can compress and damage pituitary tissue, interfering with hormone production. A tumor can also compress the optic nerves, causing visual disturbances.
In addition to tumors, certain diseases or events that cause damage to the pituitary gland may also trigger hypopituitarism. Examples include:
In some cases, hypopituitarism is caused by a genetic mutation (inherited). These mutations affect the pituitary gland's ability to produce one or more of its hormones, often starting at birth or in early childhood.
Tumors or diseases of the hypothalamus, a portion of the brain situated just above the pituitary, also can cause hypopituitarism. The hypothalamus produces hormones of its own that directly affect the activity of the pituitary gland.
In some cases, the cause of hypopituitarism is unknown.
The first step in treating hypopituitarism is often medication to help your hormone levels return to normal. This is usually called hormone replacement, because the dosages are set to match the amounts that your body would produce if it didn't have a pituitary problem. You may need to take the medication for the rest of your life.
In some cases, treatment of the condition causing hypopituitarism may lead to a complete or partial recovery of your body's ability to produce pituitary hormones.
Hormone replacement medications may include:
A doctor who specializes in endocrine disorders (endocrinologist) may monitor your symptoms and the levels of these hormones in your blood to ensure you're getting the appropriate amounts.
If you're taking corticosteroids, you'll need to work with your doctor to adjust your medication dosage during times of major physical or emotional stress. During these times, your body would usually produce extra cortisol hormone to help you manage the stress.
The same kind of fine-tuning of dosage may be necessary when you have the flu, experience diarrhea or vomiting, or have surgery or dental procedures. Adjustments in dosage may also be necessary during pregnancy or with marked changes in weight.
You may need periodic CT or MRI scans to monitor a pituitary tumor or other diseases causing hypopituitarism. Treatment for pituitary tumors may involve surgery to remove the growth. In some cases, radiation treatment or medications are recommended to control the underlying cause.
If you have hypopituitarism, it's important to wear a medical alert bracelet or pendant and carry a special card notifying others — in emergency situations, for example — of your condition. This is especially important if you're taking corticosteroids for an ACTH deficiency.