The pituitary gland is found at the base of the brain. It produces several important hormones that control the production of other hormones made by glands in the body. In panhypopituitarism, the gland produces an insufficient amount of hormones.
Compression of the tumor on local structures, especially the nerves of the eyes, can cause:
Loss of visual field
Poor temperature control
Insufficient levels of gonadotropins
In premenopausal women—missed menstrual cycles,
osteoporosis, vaginal dryness, loss or reduction in female characteristics
erectile dysfunction, reduced size of testes, decreased production of sperm,
infertility, breast enlargement, reduced muscle mass, loss or reduction in male characteristics like beard growth
Insufficient levels of growth hormone
In children—stunted growth or dwarfism
obesity, reduced cardiac output, low blood sugar levels, and reduced exercise tolerance
Insufficient levels of thyroid-stimulating hormones
can lead to:
Underactive thyroid, which causes confusion, hair loss, weakness, slow heart rate, muscle stiffness, intolerance to cold,
constipation, weight gain, and dry skin
Insufficient corticotrophic levels
can lead to:
Underactive adrenal gland, which causes low blood pressure,
low blood sugar, fatigue, weight loss, vomiting, and low stress tolerance (this can be life-threatening)
Decreased prolactin levels
In women—missed periods, infertility, and milk secretion
In men—reduced facial and body hair, small testes
Insufficient antidiuretic hormone (rare) can cause:
Excessive thirst and frequent urination
You will be asked about your symptoms and medical history. A physical exam will be done.
Tests may include the following:
Blood tests—to measure pituitary, as well as target gland hormone levels
Stimulation tests—to test the maximum capacity of the endocrine glands, usually of the pituitary gland
Semen analysis—in males suspected of infertility
—imaging test used to assess internal structures
Talk with your doctor about the best plan for you. Treatment depends on the cause of the condition. The goal of treatment is to restore normal blood hormone levels of thyroid, adrenal, estrogen or testosterone, and sometimes growth hormone.
Treatment options include:
Hormone replacement therapy—based on what types of hormones are missing
Tumor removal—done if the cause of the damage is a tumor
Radiation therapy—done if the cause of the damage is a cancer or a tumor that cannot be removed with surgery
In most cases, the causes of panhypopituitarism are not preventable.
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Hypopituitarism in children. Stanford Children's Health website. Available at: http://www.stanfordchildrens.org/en/topic/default?id=hypopituitarism-in-children-90-P01962. Accessed March 6, 2018.
Randeva HS, Schoebel J, et al. Classical pituitary apoplexy: clinical features, management and outcome. Clin Endocrinol (Oxf). 1999;51(2):181-188.
Schneider HJ, Aimaretti G, Kreitschmann-Andermahr I, Stalla GK, Ghigo E. Hypopituitarism. Lancet. 2007;269(9571):1461-1470.
Toogood AA, Stewart PM. Hypopituitarism: clinical features, diagnosis, and management. Endocrinol Metab Clin North Am. 1998;37(1):235-261
What is a growth disorder? Nemours Kids Health website. Available at: http://kidshealth.org/parent/medical/endocrine/growth_disorder.html. Updated July 2014. Accessed March 6, 2018.
Last reviewed March 2018 by
EBSCO Medical Review Board
Alan Drabkin, MD
Last Updated: 3/1/2013
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