Pituitary tumours develop in the pituitary gland, which is located behind your eyes. The pituitary gland is connected to the brain via the hypothalamus, and are both considered to be primary endocrine glandsglands responsible for the production and secretion of hormones of the body.
The pituitary gland is composed of two main portions: the anterior pituitary and posterior pituitary. The anterior pituitary is the larger, frontal portion of the pituitary gland. This portion of the gland produces and secretes hormones that control other endocrine glands, including growth hormonea chemical substance produced by glands in the endocrine system that regulates various functions in the body (also known as GH or somatotropin), thyroid-stimulating hormone (also known as TSH or thyrotropin), adrenocorticotrophic hormone (also known as ACTH or corticotropin), luteinizing hormone (also known as LH or a gonadotropin), follicle-stimulating hormone (also known as FSH or a gonadotropin), and prolactin. The posterior pituitary is the smaller, back portion of the pituitary gland. This portion of the gland stores and secretes hormones produced by the hypothalamus, including vasopressin (also known as the antidiuretic hormone or ADH) and oxytocin.
Pituitary tumours are more common in women, and tend to develop in people between the ages of 30 and 40. However, this disease can affect anyone.
Types of Pituitary Tumours
Pituitary tumours can be classified by how the cancera disease where abnormal cells split without control and spread to other nearby body tissue and/or organs cellsthe basic structural and functional unit of all living things look under the microscope, as well as whether they are functional tumourstumours that produce and secrete hormones or non-functional tumourstumours that do not produce and secrete hormones.
Pituitary Adenomas
Pituitary adenomas (non-cancerous or benignnot cancerous, can grow but will not spread to other body parts tumours) are the most common type of pituitary tumoura tissue mass that forms from groups of unhealthy cells. These types of tumours are slow growing, rarely metastasise and can be asymptomatic. Pituitary adenomas can be functional or non-functional, and are usually found in the anterior pituitary lobe.
Functional Pituitary Adenoma – Prolactinoma
Prolactinomas, or lactotroph adenomas, are the most common type of functional pituitary adenomaa benign tumour that develops from the epithelial lining of glands in the body. These tumours produce excess prolactin hormone, which is responsible for milk production in females. These tumours often have a good prognosisto predict how a disease/condition may progress and what the outcome might be.
Functional Pituitary Adenoma – Somatotropinomas
Somatotropinomas, or Somatotropin adenomas, are the functional pituitary tumours that produce and secrete excess growth hormone (GH). GH promotes body growth throughout childhood, and can cause giantism or acromegaly if too much is produced in children or in adults. These tumours often have a good prognosis.
Functional Pituitary Adenoma – Corticotropinoma
Corticotropinomas, or corticotroph adenomas, are the functional pituitary tumours that produce and secrete excess adrenocorticotrophic hormone (ACTH). ACTH promotes the growth of the adrenal glands, as well as steroid hormone production. Too much ACTH can cause Cushing’s disease. These tumours can have a good prognosis when caught early.
Functional Pituitary Adenoma – Gonadotropinoma
Gonadotropinomas, or gonadotroph adenomas, are the functional pituitary adenomas that produce luteinising hormone (LH) and follicle-stimulating hormone (FSH). In women, LH and FSH regulate the menstrual cycle and ovulation, and signal for the production of the female hormone’s oestrogen and progesterone. In males, LH and FSH control sperm production and signal for the production of testosterone. Excess levels of these hormones can cause severe fertility issues. These tumours are very rare.
Functional Pituitary Adenoma – Thyrotropinoma
Thyrotropinoma, or thyrotroph adenomas, are functional pituitary tumours that produce and secrete excess thyroid-stimulating hormone (TSH). TSH promotes growth of the thyroid gland, and produces thyroid hormones that regulate the body’s metabolism. Excess TSH could result in hyperthyroidism. These tumours are very rare.
Functional Pituitary Adenoma – Plurihormonal
In rare cases, a pituitary tumour may secrete two or more pituitary hormones. This is called a Plurihormonal adenoma, and may involve a combination of treatments to counteract the effects of multiple hormones in excess.
Non-functional Pituitary Adenomas
Non-functional pituitary adenomas, or null cell adenomas, do not produce or secrete hormones. They are often asymptomatic when small, but as they grow may cause symptoms. These tumours can have a good prognosis.
Plurihormonal Pituitary Adenomas
In rare cases, functional pituitary adenomas can produce more than one hormone. The most common combination is production of growth hormone and prolactin.
Pituitary Carcinomas
Pituitary carcinomas (cancer arising from cells lining tissues and organs) are incredibly rare. In many cases, they are functional tumours and act like functional pituitary adenomas. Pituitary adenomas and carcinomas are indistinguishable under the microscope, and can only be distinguished by whether or not the tumour metastasises. In most cases, pituitary carcinomas metastasise to the brain, spinal cord or bone surrounding the pituitary gland, but can spread to other parts of the body.
Treatment
As pituitary tumours are almost always adenomas (benign), there is currently no stagingthe process of determining how big the cancer is, where it started and if it has spread to other areas and grading system for these tumours. Some of the factors your doctor may consider in regard to treatment options may include:
- Tumour size.
- Metastasiswhen the cancer has spread to other parts of the body, also known as mets (if it is not an adenoma).
- If the tumour has grown to impact portions of the brain.
- Symptoms.
- Whether it is functional or non-functional.
Your doctor may also recommend genetic testinga procedure that analyses DNA to identify changes in genes, chromosomes and proteins, which can be used to analyse tumour DNA to help determine which treatment has the greatest chance of success which analyses your tumour DNA and can determine which treatment has the greatest chance of success. They will then discuss the most appropriate treatment option for you.
Treatment options for pituitary tumours may include:
- Surgerytreatment involving removal of cancerous tissue and/or tumours and a margin of healthy tissue around it to reduce recurrence, potentially including:
- Transsphenoidal surgerya minimally invasive procedure to remove pituitary tumors by accessing them through an incision in the nose and sphenoid sinus.
- Craniotomya surgical procedure involving the temporary removal of a portion of the skull to access the brain to reach the pituitary gland.
- Radiation therapya treatment that uses controlled doses of radiation to damage or kill cancer cells.
- Chemotherapya cancer treatment that uses drugs to kill or slow the growth of cancer cells, while minimising damage to healthy cells (only used for pituitary carcinomas).
- Hormone therapymedication that alters the levels of certain hormones in the body, such as oestrogen and progesterone (used for functional tumours to inhibit excess hormone production).
- Watch and waitthe close monitoring of a cancer without giving treatment until symptoms appear or worsen (used for asymptomatic non-functional adenomas).
- Clinical trialsresearch studies performed to test new treatments, tests or procedures and evaluate their effectiveness on various diseases.
- Palliative carea variety of practices and exercises used to provide pain relief and improve quality of life without curing the disease.
Risk factors
While the cause of pituitary tumours remains unknown, the following genetic conditions may increase your riskthe possibility that something bad will happen of developing the disease:
- Multiple endocrine neoplasia type 1 (MEN 1).
- Carney complex.
- Isolated familial acromegaly.
Not everyone with these risk factors will develop the disease, and some people who have the disease may have none of these risk factors. See your general practitioner (GP) if you are concerned.
Some of the information regarding risk factors was obtained from the Pituitary Tumors Treatment (PDQ) page published by the National Cancer Institute.
Symptoms
The symptoms of a pituitary tumour will vary, depending on whether the tumour is functional and non-functional.
Non-functional Pituitary Tumour Symptoms
The symptoms of a non-functional pituitary tumour are related to the pressure that the tumour is putting on the brain and nearby nerves, and usually occur when the tumour reaches a certain size. This pressure can result in decreased hormone production, and may cause additional symptoms. These symptoms may include:
- Persistent headaches.
- Changes in vision, such as:
- Blurred vision.
- Double vision.
- Loss of peripheral vision.
- Blindness.
- Eye muscle weakness.
- Facial numbness and/or pain.
- Dizziness.
- Loss of consciousness.
- Loss of body hair.
- Changes in menstruation and milk production.
- Decreased sex drive.
- Delayed growth and sexual development (children).
- Seizures.
Functional Pituitary Tumour Symptoms.
The symptoms of a functioning pituitary tumour will vary based on the type of hormone being produced.
Excess Prolactin
The symptoms of excess prolactin have different effects in men and women.
Excess prolactin in women may cause the following symptoms:
- Changes in menstrual periods, such as:
- Irregular menstrual periods.
- Absence of menstrual periods.
- Less frequent menstrual periods.
- Unusually light menstrual periods.
- Abnormal breast milk production (also known as galactorrhea).
- Lowered sex drive.
- Infertility.
- Osteoporosis.
Excess prolactin in men may cause the following symptoms:
- Erectile dysfunctionimpaired or abnormal function; not working properly (also known as impotence).
- Lowered sperm count.
- Breast growth.
- Lowered sex drive.
- Infertility.
- Osteoporosis.
Excess Growth Hormone
The symptoms of excess GH have different effects in children and adults.
In children, excess GH may cause giantism, which has the following symptoms:
- Being unusually tall for age.
- Rapid growth.
- Joint pain.
- Increased sweating.
Full-grown adults cannot develop giantism, even with excess GH. However, they can develop acromegaly, which has the following symptoms:
- Growth of skull, hands and feet. This may cause an increase in hat, shoe, glove and/or ring size.
- Changes in vision and/or voice.
- Changes in facial appearance (such as wider spacing of teeth and/or jawbone growth).
- Joint pain.
- Increased sweating.
- Hyperglycaemiahigh blood sugar.
- Kidneya pair of bean-shaped organs in the abdomen that are responsible for filtering excess water and waste products from the blood and converting them into urine to be removed from the body stones.
- Heart disease.
- Tingling and/or numbness in the hands and fingers.
Excess ACTH
Excess ACTH may cause Cushing’s disease, or hypercortisolism, which have different effects in adults and children.
In adults, the symptoms of Cushing’s disease include:
- Unexplained weight gain (particularly in face, chest and abdominal areas).
- Exaggerated facial roundness.
- Thinning of arms and legs with muscle weakness.
- Pink or purple stretch marks on the chest and/or abdomenstomach, stomach area, belly.
- Easy bruising.
- New or increased hair growth.
- Acne.
- Hyperglycaemia.
- Hypertensionhigh blood pressure.
- Weakening of bones, which may cause osteoporosis or easily broken bones.
- Anxiety, irritability and/or depression.
Children can develop many of the same symptoms as adults with the disease. In addition to this, they may also experience:
- Delayed growth.
- Difficulty concentrating.
Excess LH & FSH
These tumours are incredibly rare, and may appear asymptomatic in the earlier stages of the disease. In most cases, they will cause the same issues as non-functioning adenomas before excess LH and FSH are produced. If the tumour becomes large enough to produces excess hormones, you may also experience the following symptoms:
- Irregular menstrual periods (women).
- Low testosterone levels (men).
- Decreased sex drive.
Excess TSH
Excess TSH may cause hyperthyroidism, which has the following symptoms:
- Unexplained weight loss.
- Tachycardiaa rapid heart rate; clinically defined as a rate of more than 100 beats per minute.
- Nervousness, anxiety and/or irritability.
- Tremors (shaking).
- Frequent bowelportion of the digestive system that digests food (small bowel) and absorbs salts and water (large bowel); also called intestines movements.
- Excessive sweating.
- A large lump in the front of the neck (enlarged thyroid gland).
Not everyone with the symptoms above will have cancer but see your GP if you are concerned.
Diagnosis
If your doctor suspects you have a pituitary tumour, they may order the following tests to confirm the diagnosisthe process of identifying a disease based on signs and symptoms, patient history and medical test results and refer you to a specialist for treatment:
- Physical examinationan examination of your current symptoms, affected area(s) and overall medical history.
- Neurological examinationan assessment of sensory and motor functions, such as vision, balance and coordination.
- Endocrine studiesstudies that involve blood, urine and/or imaging tests to analyse hormone levels.
- Blood teststesting done to measure the levels of certain substances in the blood.
- Imagingtests that create detailed images of areas inside the body tests, potentially including:
- CT (computed tomography) scana type of medical imaging that uses x-rays and computer technology to create detailed images of the body.
- MRI (magnetic resonance imaging)a type of medical imaging that uses radiowaves, a strong magnet and computer technology to create detailed images of the body.
- Biopsyremoval of a section of tissue to analyse for cancer cells.
