Prolactinoma

Prolactinoma

Overview

Prolactinoma is a noncancerous tumor of the pituitary gland. This tumor causes the pituitary gland to make too much of a hormone called prolactin. The major effect of a prolactinoma is decreased levels of some sex hormones — namely, estrogen and testosterone.

A prolactinoma isn't life-threatening. But it can cause vision difficulties, infertility and other problems. Prolactinoma is the most common type of hormone-producing tumor that can develop in the pituitary gland.

A prolactinoma can usually be treated with medications to bring the prolactin level down into the standard range and shrink the tumor. In some cases, surgery to remove the tumor might be an option.

Symptoms

A prolactinoma might not cause any signs or symptoms. However, too much prolactin in your blood (hyperprolactinemia) can cause symptoms. So can pressure on surrounding tissues from a large tumor.

Because too much prolactin can disrupt the reproductive system (hypogonadism), some of the signs and symptoms of a prolactinoma are specific to females or males.

In females, prolactinoma can cause:

Irregular menstrual periods or no menstrual periods

Milky discharge from the breasts when not pregnant or breastfeeding

Painful intercourse due to vaginal dryness

Acne and excessive body and facial hair growth

In males, prolactinoma can cause:

Erectile dysfunction

Decreased body and facial hair

Smaller muscles

Enlarged breasts

In both females and males, prolactinoma can cause:

Infertility

Weak and brittle bones that break easily (osteoporosis)

Loss of interest in sexual activity

Pressure from tumor growth can cause:

Vision problems

Headache

Reduction of other hormones produced by the pituitary gland

Females who are premenopausal tend to notice signs and symptoms early, when tumors are smaller in size. This is probably because of missed or irregular menstrual periods. Females who are postmenopausal are more likely to notice signs and symptoms later, when tumors are larger and more likely to cause headache or vision problems. Males are also more likely to notice signs and symptoms later.

Causes

Prolactinoma is one type of tumor that develops in the pituitary gland. The cause of prolactinoma is usually unknown.

The pituitary gland is a small bean-shaped gland located at the base of your brain. Despite its small size, the pituitary gland has an effect on nearly every part of your body. Its hormones help control important functions such as growth, metabolism, blood pressure and reproduction.

A prolactinoma causes the pituitary gland to make too much of a hormone called prolactin. This results in a decreased level of some sex hormones — namely, estrogen and testosterone.

Making too much prolactin (hyperprolactinemia) can also happen for reasons other than a prolactinoma. These can include:

Medications

Other types of pituitary tumors

Kidney disease

Underactive thyroid gland

Pregnancy and breastfeeding

Risk factors

More prolactinomas occur in females than males. The disorder is rare in children.

Rarely, an inherited disorder such as multiple endocrine neoplasia, type 1 — a disorder that causes tumors in hormone-producing glands — may increase the risk of a prolactinoma.

Complications

Complications of prolactinoma may include:

Infertility. A prolactinoma can interfere with reproduction. Too much prolactin reduces the production of the hormones estrogen and testosterone. Too much prolactin also can prevent the release of an egg during the menstrual cycle (anovulation) in females. In males, too much prolactin also can lead to decreased sperm production.

Bone loss (osteoporosis). Reduced estrogen and testosterone also cause decreased bone strength. This results in weak and brittle bones that can break easily.

Pregnancy complications. During a typical pregnancy, the production of estrogen increases. This may cause tumor growth. This can result in signs and symptoms such as headaches and changes in vision in pregnant females who have large prolactinomas.

Vision loss. Left untreated, a prolactinoma may grow large enough to press on your optic nerve. This nerve sits near the pituitary gland. The nerve sends images from your eye to your brain so that you can see. The first sign of pressure on the optic nerve is a loss of your side (peripheral) vision.

Low levels of other pituitary gland hormones. Larger prolactinomas can put pressure on the healthy part of the pituitary gland. This can lead to lower levels of other hormones controlled by the pituitary gland. These include thyroid hormones and cortisol. Cortisol is a stress-response hormone.

Diagnosis

If you have signs and symptoms that suggest you have a prolactinoma, your health care provider may recommend:

Blood tests. Blood tests can show if too much prolactin is being made. They can also show whether levels of other hormones controlled by the pituitary gland are within the standard range. A pregnancy test is typically recommended for females of childbearing age.

Brain imaging. Your provider may be able to detect a prolactinoma using a magnetic resonance imaging (MRI) scan of your brain.

Vision tests. These can determine if a prolactinoma is affecting your sight.

Your provider may also refer you for additional testing with a specialist in treating disorders that affect the endocrine glands and hormones (endocrinologist).

Treatment

Goals in the treatment of a prolactinoma include:

Return the production of prolactin to within the standard range

Reduce the size of the prolactinoma

Restore healthy pituitary gland function

For most people, treatment can eliminate or improve:

Problems caused by increased prolactin levels, such as irregular menstrual periods, infertility and loss of interest in sexual activity

Signs or symptoms from tumor pressure, such as headaches or vision problems

Prolactinoma treatment includes two main therapies: medications and surgery.

Medications

Oral medications known as dopamine agonists are generally used to treat a prolactinoma. These drugs mimic the effects of dopamine — the brain chemical that controls how much prolactin is made. Dopamine agonists can decrease the production of prolactin and shrink the size of the tumor. Drugs can eliminate symptoms for most people with prolactinomas. However, you'll generally need long-term treatment with drugs.

Commonly prescribed drugs include cabergoline and bromocriptine (Cycloset, Parlodel).

If a drug shrinks the tumor significantly and your prolactin level remains within the standard range for two years, you may be able to taper off the drug. Only taper off your drug with your health care provider's guidance. Your provider monitors your prolactin levels during this process. Don't stop taking your drug without talking to your provider first.

Prolactin levels commonly rise after stopping the drug. If this happens, your provider will likely ask you to restart taking the drug.

Common medication side effects

Common side effects of these medications include nausea and vomiting, dizziness, nasal stuffiness, and headache. However, these side effects often can be less bothersome if your health care provider starts you with a very low dose of the drug. Then your provider can gradually increase the dose. It may also help if you take the drug with food or if you take it at bedtime.

People have rarely had heart valve damage with cabergoline. But it's usually in people taking much higher doses for Parkinson's disease. Some people may develop impulse control disorders, such as compulsive gambling, while taking these drugs.

Medication during pregnancy

Both bromocriptine and cabergoline treat prolactinomas in people who want to become pregnant. But the medications have different advantages and disadvantages. Discuss the pros and cons of these options with your health care provider. Together you can decide which drug may work best for you.

In most situations, a provider typically advises stopping the drug when pregnancy is confirmed. Although both drugs are considered safe in pregnancy, your provider will generally recommend avoiding any drug during pregnancy when possible. However, if you have a large prolactinoma or you develop signs and symptoms such as headaches or vision changes, your provider may recommend that you restart the drug. This can prevent further tumor growth and complications.

If you're being treated for a prolactinoma and you'd like to start a family, it's best to discuss your options with your provider before you become pregnant.

Surgery

Surgery to remove a prolactinoma is generally an option if drug therapy doesn't work or you can't tolerate the drug. Surgery may be necessary to relieve pressure on the nerves that control your vision.

The type of surgery you have will depend largely on the size and extent of your tumor:

Nasal surgery. For most people who need surgery, the procedure involves removing the tumor through the nose (nasal cavity). This surgery is called transsphenoidal surgery. Complication rates are low because the surgeon doesn't touch other areas of the brain during surgery. This surgery leaves no visible scars.

Transcranial surgery. If your tumor is large or has extended to nearby brain tissue, you may need this procedure, also known as a craniotomy. The surgeon removes the tumor through the upper part of the skull.

Surgery outcomes depend on the size and location of the tumor and prolactin levels before surgery. The surgeon's skill and experience with this specific type of surgery also is a factor. Sometimes an MRI scan shows that a prolactinoma has extended to areas in the brain where it's unsafe to attempt removal. When this happens, the surgeon can only partially remove the prolactinoma.

Surgery corrects the prolactin level in most people with small prolactinomas. However, tumors may come back within several years of surgery. For people with larger tumors that can only be partially removed, drug therapy often can return the prolactin level to the standard range after surgery.

Radiation

Rarely, radiation therapy to kill tumor cells may be an option for a large prolactinoma. You may have radiation if you don't respond to medication, if you aren't able to have surgery, or if your surgery didn't remove all of a large tumor.

Type of Doctor Department : Neurosurgeons and otolaryngological (ENT) surgeons.