Types of Pituitary Tumors

Houston Methodist has access to advanced technology to detect, diagnose and treat pituitary adenomas (noncancerous), pituitary carcinomas (cancerous) and other types of tumors that grow in and around the pituitary gland. Our neurosurgeons work collaboratively and seamlessly with doctors from other areas of medicine so patients benefit from the full breadth of Houston Methodist excellence.
Most pituitary tumors can be treated. Virtually all tumors can be removed surgically or reduced in size with other means, and prognosis for patients is excellent.

There are four main categories of pituitary tumors, and the first category includes several tumors that are very different from one another:
Pituitary Adenomas
Pituitary adenomas are benign (noncancerous) growths commonly found in about one percent of the population and often cause the gland to produce too much or too little of a certain hormone. 
Pituitary adenomas are classified based on their size and whether or not they produce hormones.
Microadenomas are smaller than 1 cm (less than half an inch) in diameter.
Macroadenomas are larger than 1 cm in diameter.
About half of all pituitary adenomas are endocrine-active (functional) tumors that secrete hormones. They are usually found when looking for the cause of a hormonal imbalance.
Pituitary adenomas that do not produce hormones are called endocrine-inactive or nonfunctional tumors. They are usually found incidentally, often when a brain scan is performed for another reason. They can also cause of vision even to blindness, which can be reversed by pituitary surgery in some cases.

Endocrine-active Tumors
Endocrine-active tumors account for about half of all pituitary adenomas and are usually found when looking for the cause of a hormonal imbalance. Excessive hormone production can have a significant impact on the body. When certain hormones are in overdrive, they can lead to serious syndromes that have far-reaching health consequences. Most pituitary adenomas secrete growth hormones, adrenocortiotropin (adrenocortiotropic hormone, ACTH), prolactin, or less often, thyroid-stimulating hormone (TSH). The symptoms of endocrine-active tumors depend on what hormones the tumor secretes.

Growth Hormone and Acromegaly
Growth hormone is necessary for normal growth in children and helps adults maintain healthy bone and muscle tissue. Pituitary adenomas that cause overproduction of growth hormone in adults can lead to acromegaly, or enlarged bones in the hands, feet and face, accompanied by other symptoms:
Shoes and rings no longer fit
Fingers and/or toes becoming wider
Hands feeling soft, like bread dough
Enlarged forehead, jaw, nose, lips and/or tongue
Spaces between teeth becoming wider
Voice deepening in males
Skin changes, including skin tags, oily skin and excessive sweating
Carpal tunnel syndrome (due to enlarged wrist tissue)
Sleep apnea

Because the physical changes take place slowly, it can take years before acromegaly is diagnosed. Long-term or untreated acromegaly is a life-threatening disorder, and people age 45 and older have a death rate twice that of people without the disease, normally as a result of heart attack or stroke. Long-term or untreated acromegaly can lead to high blood pressure, heart disease, type 2 diabetes, thyroid cancer and colon polyps.
Although rare in children, pituitary tumors that increase growth hormone can lead to gigantism if the child has not reached puberty.

Adrenocorticotropic Hormone (ACTH) and Cushing's Disease
The pituitary produces ACTH, which triggers the adrenal glands, to produce cortisol. Cortisol is a body steroid that helps regulate blood pressure, cardiovascular function and the metabolism of proteins, carbohydrates and fats. It also reduces the body’s inflammatory response, helps insulin break down sugar for energy and helps the body respond to stress. 
Pituitary tumors can occur in cells that make ACTH, resulting in excessive cortisol in the body. When this occurs, it creates a collection of symptoms known as Cushing’s disease. 
Although fairly rare, Cushing’s disease affects women five times more than men, and is most common among adults 20 to 50 years old. It is also associated with high blood pressure that is often hard to control, diabetes, irritability, anxiety and depression. Left untreated, this disease is a fatal disorder.

Cushing’s disease is associated with a wide range of symptoms:
Upper-body obesity with thin arms and legs
Collection of fat between the shoulders (buffalo hump)
Rounded face (sometimes called moon face)
Increased fat around the neck
Severe fatigue
Weak muscles
Bone pain
Thin and fragile skin that bruises easily
Purple marks on the abdomen, thighs, buttocks, arms and breasts
Women grow more hair on their faces, necks, chests, abdomens and thighs
Menstrual cycles may be irregular or stop
Men have lower libido (sex drive) and fertility
Thin, weakened bones resulting in rib and spine fractures from everyday activities
Obesity and slow growth in children
Mental changes

Some pituitary adenomas produce excess prolactin (hyperprolactinemia), which decreases estrogen levels in women and testosterone levels in men. This disrupts the reproductive system and can lead to infertility. The tumor’s location can impair vision, which is often the first symptom people notice. Other symptoms include low bone density, low levels of other hormones (hypopituitarism), low sex drive and headaches.
General symptoms of prolactinoma can include the following conditions:
Low bone density
Low levels of other hormones (hypopituitarism) due to pressure from the tumor
Low sex drive
Vision problems

Prolactinoma affects sex hormones; therefore, women and men may have different symptoms. Prolactinoma symptoms that can occur in women include the following:
Irregular menstrual cycle or no periods at all
Milky discharge from breasts when not pregnant or breastfeeding
Vaginal dryness, leading to painful sex
Excessive face and body hair

In men, symptoms may include erectile dysfunction and enlarged breasts, and may not be noticed until the tumor is large and the patient begins to experience headaches or vision problems.

Thyroid-Stimulating Hormone Secreting Tumors
These tumors cause excessive TSH production, which causes the thyroid to produce too much thyroid hormone. TSH-secreting tumors are rare, but people who have them will have the symptoms characteristic of an overactive thyroid (hyperthyroidism):
Unexplained weight loss
Rapid or irregular heart beat
Shaking or tremors
Increased appetite
Sweating or feeling hot
Frequent bowel movements
Trouble falling asleep
Enlarged thyroid (lump in the front of the neck)

Endocrine-Inactive (Nonfunctional) Tumors
Endocrine-inactive or nonfunctional tumors do not secrete active hormones, although they may sometimes secrete a defective hormone that has no endocrine effects. Because these types of pituitary adenomas do not alter hormone levels, they are often found during a brain scan for some other reason, or after they have grown large enough to exert pressure on surrounding tissues or structures, producing symptoms:
Headaches that get progressively worse
Loss in peripheral vision (the extreme left or right sides of what you see) or double vision
Severe vision loss, including blindness
Increased pressure in the brain
Problems with memory, weakness or numbness if the tumors are very large and press on other areas of the brain

Treating Pituitary Adenomas
Our specialists at Houston Methodist offer many treatment options to remove or shrink pituitary tumors, making it possible to devise the best options to treat your pituitary adenoma:
Standard surgical removal of the pituitary tumor 
Precisely focused, minimally invasive radiation therapy  
Hormone therapy
Pituitary Carcinomas
Pituitary carcinomas are very rare, cancerous tumors that make up just 0.2 percent of all pituitary adenomas. They are equally common in women and men, most often occurring in middle age. Symptoms often mimic those of pituitary adenomas, as most pituitary carcinomas also secrete hormones. Because they are so rare and share symptoms of pituitary adenomas, pituitary carcinomas are sometimes discovered after they have spread to other parts of the body. They can be hard to treat, and require aggressive treatment, which may include surgery, radiation and chemotherapy.

Rathke's Cleft Cysts
Rathke's cleft cysts occur during fetal development when the pituitary gland does not properly form. During normal development, the pituitary gland forms as a result of downward growth of the brain into the posterior lobe, and the upward growth of cells that become the secreting part of the gland, called the anterior lobe. There is a little pouch or cavity between the two lobes that seals by birth, and the two parts of the gland become one. When the pouch does not seal, the cells secrete a mucinous substance that causes progressive enlargement (Rathke’s cleft cysts). It is important to monitor these cysts carefully with frequent MRI brain scans to ensure they are not getting larger.

Craniopharyngiomas are tumors that occur near the pituitary stalk and form as result of deficiencies in normal endocrine development. They are usually benign (noncancerous) and are typically diagnosed when they grow large enough to exert pressure on the brain, optic nerve or pituitary gland, and cause the following symptoms:
Delayed growth in children
Vision problem or swollen optic nerve
Excessive thirst and urination

Adamantinomatous (ordinary) craniopharyngiomas are less solid (with cysts) tumors that tend to affect children under 14 years of age. These tumors account for 5 to 10 percent of all childhood brain tumors.

Papillary craniopharyngiomas are more solid tumors and typically found in adults over age 45. 
Craniopharyngiomas are more common in African Americans.

Surgery is usually the first line of treatment, followed by radiation (in adults and children 3 years and older).

Patient Stories
Perhaps the best way to learn about our highly trained neurologists, neuro-oncologists and neurosurgeons at Houston Methodist is through our patients. We invite you to read about their inspiring patient stories and their experience of being a patient at Houston Methodist.

Marcie Lester — Learn how Peak Center specialists successfully removed Marcie Lester's pituitary tumor and helped her return to her normal routines.

Belinda Amboree — Learn how Houston Methodist physicians used state-of-the-art technology to detect and treat Belinda Amboree's pituitary tumor.

Jed Duplantis – At Houston Methodist Jed underwent successful endoscopic pituitary surgery when his doctors discovered he had a large pituitary tumor pressing on his optical nerves.

Download our brochure  to learn more about causes, detection and treatment of pituitary tumors.

Clinical Trials
Doctors at Houston Methodist are engaged in many clinical trials of drugs and other treatment options that are still in development. To find out more about active clinical trials related to brain tumors, please visit the following:


Our physicians at Houston Methodist specialize in pituitary tumors at the following convenient locations.