Pituitary Adenoma
(Pituitary Tumor; Nervous System Tumor)
Definition
| Pituitary Gland |
|
| Copyright © Nucleus Medical Media, Inc. |
Causes
Risk Factors
- A family or personal history of multiple endocrine neoplasia, type 1 (MEN1) —a hereditary condition that increases the risk of developing pituitary, hypothalamus, and parathyroid and pancreatic tumors
- Other disorders that run in the family like Carney complex or acromegaly (giantism)
Symptoms
- Headache
- Blurred vision or tunnel vision
- Milk production from nonlactating females
- Loss of or irregular periods
- Loss of sex drive
- Vaginal dryness
- Low bone density or osteoporosis
- Enlarged thyroid (eg goiter)
- Tremors
- Heart palpitations
- Anxiety
- Weight loss
- Insomnia
- Menstrual disturbance
- High blood pressure
- High fasting glucose
- Skin changes (increased facial hair, acne, bruising, bluish stretch marks
- Buffalo hump (increased fatty tissue in back)
- Obesity especially around the wrist
- Round face
- Acromegaly (adult)
- Gigantism (child)
- High blood pressure
- High fasting blood sugar
- Facial features coarse
- Oily skin
- Excess sweating
- Diabetes mellitus
- Kidney stones
- Cardiovascular disease
- High blood pressure
- Osteoporosis
- Thyroid disease
Diagnosis
- Blood tests—to measure pituitary and other gland (prolactin, TSH, FT4, IGF-1, growth hormone, corticotrophin or ACTH, beta human gonadotropin, alpha subunit, estradiol, testosterone), hormone levels, blood sugar levels and to identify other underlying conditions that may be causing your symptoms
- Urine tests—to measure excretion levels of certain pituitary gland hormones (beta human gonadotropin, cortisol)
- Visual field tests—to check for problems with peripheral vision
- MRI scan —a test that uses strong magnets and radio waves to create pictures of the pituitary gland near the brain
- Glucose tolerance test—the standard test for acromegaly
- Dexamethasone suppression test and corticotropin-releasing hormone (CRH) test—best tests to see if excessive secretion of hormones from the adrenal gland is due to a pituitary adenoma
Treatment
Surgery
Medications
- Dopamine agonists (eg cabergoline, bromocriptine)
- Octreotide or long-acting versions
Radiation Therapy
- Conventional therapy—radiation is directed at the pituitary from a source outside the body
- Stereotactic radiosurgery—an intense radiation beam is targeted directly at the tumor
- Proton beam radiotherapy—a beam of protons (positively charged particles) is directly focused on the tumor
RESOURCES
American Cancer Society http://www.cancer.org/
Hormone Foundation http://www.hormone.org/
Pituitary Network Association http://www.pituitary.org/
CANADIAN RESOURCES
Canadian Cancer Society http://www.cancer.ca/
Canadian Health Network http://www.canadian-health-network.ca/
References
Becker A, Daly AF: The clinical, pathological, and genetic features of familial isolated pituitary adenomas. Eur J Endocrinol 2007;57:371-82.
Beshay VE, Beshay JE, Halvorson LM: Pituitary tumors: diagnosis, management, and implications for reproduction. Semin Reprod Med 2007;25:388-401.
Detailed guide: pituitary tumor. American Cancer Society website. Available at: http://www.cancer.org/docroot/CRI/CRI%5F2%5F3x.asp?rnav=cridg&dt=61 . Accessed November 8, 2005.
Pituitary tumors information page. National Institute of Neurological Disorders and Stroke website. Available at: http://www.ninds.nih.gov/disorders/pituitary%5Ftumors/pituitary%5Ftumors.htm . Accessed November 8, 2005.
Pituitary tumors (PDQ): treatment. National Cancer Institute website. Available at: http://www.cancer.gov/cancertopics/pdq/treatment/pituitary/patient . Accessed November 8, 2005.
Revision Information
- Reviewer: Konda Mohan Reddy, MD, FAAP
- Review Date: 04/2012 -
- Update Date: 00/40/2012 -
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