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(PHP; Underactive Pituitary Gland)
  • Definition

    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.
    Pituitary Gland
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  • Causes

    This condition is most often caused by damage to the gland. In adults, it is usually a result of pituitary surgery. In children, damage to the pituitary gland may be caused by:
    • Infection
    • Stroke
    • Genetic factors
    • Tumor on or near the pituitary gland
    • Cancer that has spread
    • Injury
    • No known cause
  • Risk Factors

    These risk factors increase your chance of developing panhypopituitarism. Tell your doctor if you have any of these risk factors:
  • Symptoms

    Compression of the Tumor
    Compression of the tumor on local structures, especially the nerves of the eyes, can cause:
    • Blurred vision
    • Loss of visual field
    • Poor temperature control
    Insufficient Hormones
    • Insufficient levels of gonadotropins can cause:
      • In premenopausal women: missed menstrual cycles, infertility , osteoporosis , vaginal dryness, loss or reduction in female characteristics
      • In men: impotence , reduced size of testes, decreased production of sperm, infertility , breast enlargement, reduced muscle mass, loss or reduction in male characteristics (eg, beard growth)
    • Insufficient levels of growth hormone can cause:
      • In children: stunted growth or dwarfism
      • In adults: weakness, 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.
    • Excessive prolactin levels can cause:
      • 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
      • Night-time urination
  • Diagnosis

    Your doctor will ask about your symptoms and medical history. A physical exam will be done.
    Tests may include the following:
    • MRI scan —a test that uses magnetic waves to make pictures of structures inside the body
    • Blood tests—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
  • Treatment

    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 tumor
  • Prevention

    The majority of causes are not preventable. Injury prevention can prevent some cases.

    The Hormone Foundation

    The Pituitary Network


    About Kids Health

    Health Canada


    Bhasin S, Cunningham GR, Hayes FJ, et al. Testosterone therapy in adult men with androgen deficiency syndromes: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2006;91:1995-2010.

    Diabetes & other endocrine and metabolic disorders: hypopituitarism. Lucile Packard Children's Hospital website. Available at: Accessed May 30, 2007.

    Geffner M. Panhypopituitarism. The Magic Foundation website. Available at: Accessed May 30, 2007.

    Randeva HS, Schoebel J, Byrne J, et al. Classical pituitary apoplexy: clinical features, management and outcome. Clin Endocrinol (Oxf) . 1999;51:181-188.

    Schneider HJ, Aimaretti G, Kreitschmann-Andermahr I, et al. Hypopituitarism. Lancet. 2007;269:1461-1470.

    Toogood AA, Stewart PM. Hypopituitarism: clinical features, diagnosis, and management. Endocrinol Metab Clin North Am. 1998;37:235-261

    What is a growth disorder? Nemours Foundation website. Available at: Accessed May 30, 2007.

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