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Pituitary Tumor


Overview, Causes, & Risk Factors

A pituitary tumor is an abnormal growth that develops within the pituitary gland. The pituitary is a pea-sized gland at the base of the brain. It secretes hormones into the bloodstream. These hormones control most of the other glands in the body that secrete hormones.

What is going on in the body?

The pituitary gland has three parts or lobes.

  • The anterior or front lobe controls growth, thyroid function, and breast milk production.
  • The intermediate or middle lobe controls darkening of the skin.
  • The posterior or back lobe controls urine production and uterine contractions during childbirth.
  • Pituitary tumors comprise about 10% of all brain tumors. They generally develop from the anterior lobe and are rarely caused by cancer. When the tumor enlarges, it generally grows upward. It can press on other structures, such as the optic nerves. The optic nerves carry visual signals, so vision is often affected. Pituitary tumors can also interfere with:

  • growth hormone
  • male hormone production
  • milk production
  • What are the causes and risks of the condition?

    The exact cause of pituitary tumors is unknown. Women face a higher risk of developing pituitary tumors than men.


    Symptoms & Signs

    What are the signs and symptoms of the condition?

    A pituitary tumor can cause symptoms that fall into two groups:

  • general, which are common to all tumors regardless of cell type
  • specific, which are characteristic of the cell type involved
  • General symptoms include:

  • headache
  • visual impairment, most commonly the loss of vision in the outside top quarter of the visual field in both eyes
  • weakness
  • Depending on the cell type making up the tumor, symptoms may include:

  • abnormal secretion of breast milk
  • absence of menstrual periods
  • appearance of purplish marks on the skin
  • decreased sex drive in males
  • development of a hump on the person's back, near the base of the neck
  • excessive enlargement of the hands, feet, and facial features
  • excessive growth
  • hair loss and skin coarseness
  • intolerance to cold
  • rounded, "moonlike" facial features

  • Diagnosis & Tests

    How is the condition diagnosed?

    Diagnosis of a pituitary tumor begins with a history and physical exam. The healthcare provider may order tests, including:

  • blood and urine tests to measure the levels of different hormones
  • a cranial CT scan and cranial MRI scan to show the tumor itself
  • a skull X-ray to show enlargement or erosion of the skull bones
  • visual field testing to see if the tumor is pressing on the optic nerve

  • Prevention & Expectations

    What can be done to prevent the condition?

    There is no known way to prevent pituitary tumors.

    What are the long-term effects of the condition?

    Pituitary tumors enlarge at varying rates. Untreated tumors may eventually lead to blindness by damaging the optic nerves. After 75% of normal pituitary cells are destroyed, all pituitary function may eventually be lost.

    What are the risks to others?

    Pituitary tumors are not contagious, and pose no risk to others.


    Treatment & Monitoring

    What are the treatments for the condition?

    Many pituitary tumors can be removed surgically. The operation usually takes place through the head for larger tumors and through the nose for smaller ones. Radiation therapy can shrink some tumors. Medicines, such as bromocriptine, can shrink certain tumors that affect breast milk production.

    What are the side effects of the treatments?

    Surgery carries a risk of bleeding, infection, or allergic reaction to anesthesia.

    What happens after treatment for the condition?

    Treatment, even if successful, may not correct the visual impairment. Most people will require some form of hormone replacement medicine, even after successful surgery.

    How is the condition monitored?

    The individual will have regular visits with the healthcare provider. Any new or worsening symptoms should be reported to the provider.


    Attribution

    Author:James Warson, MD
    Date Written:
    Editor:Crist, Gayle P., MS, BA
    Edit Date:08/10/01
    Reviewer:William M. Boggs, MD
    Date Reviewed:08/13/01

    Sources

    http://www.nci.nih.gov


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