Specific goals in the treatment of prolactinoma include:
- Return the production of prolactin to normal levels
- Restore normal pituitary gland function
- Eliminate galactorrhea
- Reduce the size of the pituitary tumor
- Eliminate any signs or symptoms from tumor pressure, such as headaches or vision problems
Prolactinoma treatment consists of two main therapies, medications and surgery:
Medications
Oral medications often can decrease the production of prolactin and eliminate symptoms. Medications may also shrink the tumor. However, long-term treatment with medications is generally necessary.
Doctors use drugs known as dopamine agonists to treat prolactinoma. These drugs mimic the effects of dopamine — the brain chemical that normally controls prolactin production — but are much more potent and long lasting. Commonly prescribed medications include bromocriptine (Parlodel) and cabergoline. These drugs decrease prolactin production and may shrink the tumor in most people with prolactinoma.
Medications and pregnancy
Bromocriptine is the preferred drug when treating women who want to restore their fertility because its safety in pregnancy is well established. During pregnancy, you're doctor will likely advise you to stop taking bromocriptine or carbergoline.
Although these medications are considered safe during pregnancy, doctors generally prefer to keep medications to a minimum while you're pregnant. However, if you have a very large tumor, your doctor may recommend that you stay on your medication during your pregnancy to prevent complications from the prolactinoma. If you're being treated for prolactinoma and you'd like to start a family, it's best to discuss your options with your doctor before you become pregnant.
Medication side effects
Common side effects of these medications include lightheadedness, nausea and nasal stuffiness. However, these side effects often can be minimized if your doctor starts you with a very low dose of medication and gradually increases the dose. Rarely, cabergoline use has been associated with heart valve damage.
If medication effectively shrinks the tumor and your prolactin level remains normal afterward, you may be able to eventually stop taking the medication. Your doctor can offer you advice on when this may be possible for you.
Surgery
If drug therapy for the treatment of prolactinoma doesn't work or you can't tolerate the medication, surgery may be an option for the removal of a pituitary tumor. It may also be necessary to relieve pressure on the nerves that control your vision.
The type of surgery you have depends largely on the size and extent of your tumor:
- Transsphenoidal surgery. Most people who need surgery have a transsphenoidal procedure. In this surgery, the tumor is removed through the nasal cavity. Complication rates from this type of surgery are low because no other areas of the brain are touched during surgery, and this surgery leaves no visible scars.
- Transcranial surgery. Transsphenoidal surgery may not be best for some large tumors, or for tumors that have spread to nearby brain tissue. If this is the case for you, you may need a transcranial procedure, also known as a craniotomy. This procedure involves accessing the tumor through the upper part of the skull.
The outcome of surgery depends on the size and location of the tumor and your prolactin levels before surgery. The higher the prolactin level, the slimmer the chance that your prolactin production will return to normal after surgery. Surgery corrects the prolactin level in most people with small pituitary tumors. However, many pituitary tumors come back within five years of surgery. For people with larger tumors that can only be only partially removed, drug therapy often can return the prolactin level to a normal range after surgery.
Radiation
For people who don't respond to medication and aren't candidates for surgery, radiation therapy may be an option.
©1998-2012 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
Read this article on Mayoclinic.com.