Acromegaly
Definition |
Causes |
Risk Factors |
Symptoms |
Diagnosis |
Treatment |
Prevention |
Organizations
Definition
Acromegaly is a rare disorder of excessive growth in adults. It affects the bones and soft tissues. Children suffer from a similar condition called gigantism.
Causes
In most cases, acromegaly is caused by over-secretion of growth hormone (GH) produced by a benign tumor of the pituitary gland. The pituitary gland is a small gland located at the base of the brain that produces many hormones. In a small number of cases, tumors of other organs may be the source of excess GH.
Risk Factors
A risk factor is something that increases your chances of getting a disease or condition. Some rare cases of acromegaly are hereditary. No other risk factors have been identified.
Symptoms
Symptoms usually develop very slowly over time. Acromegaly can cause serious complications and premature death if not treated.
In children, excess GH production causes elongation of the bones and associated soft tissue swelling. If not treated, children with this disorder can grow to a height of 7-8 feet.
Symptoms and complications in adults may include the following:
- Abnormally large growth and deformity of the:
- Hands (rings no longer fit)
- Feet (need a bigger size shoe)
- Face
- Jaw (teeth do not line up correctly when the mouth is closed)
- Lips
- Tongue
- Carpal tunnel syndrome
- Skin changes, such as:
- Thickened, oily, and sometimes darkened skin
- Severe acne
- Excessive sweating and offensive body order due to enlargement of the sweat glands
- Deepening voice due to enlarged sinuses, vocal cords, and soft tissues of the throat
- Fatigue and weakness
- Sleep apnea
- Arthritis and other joint problems
- Headaches and visual problems, due to a growing tumor at the base of the brain
- Hypothyroidism
- Enlargement of the liver, kidneys, spleen, heart, and/or other internal organs, which can lead to:
- In women:
- Irregular menstrual cycles
- In some cases, galactorrhea (abnormal production of breast milk)
- In men:
Diagnosis
The doctor will ask about your symptoms and medical history and perform a physical exam. The symptoms of acromegaly develop slowly over a number of years. So it is often not diagnosed until years after its onset.
Blood tests will be done to measure the level of GH, related substances, and other pituitary hormones. A glucose challenge test may also be given to see if the GH level drops—it will not drop in cases of acromegaly. If these tests confirm acromegaly, the following may be done to locate the tumor that is causing the disorder:
- Head CT scan – a type of x-ray that uses a computer to make pictures of the inside of the brain and surrounding structures
- MRI scan – a test that uses magnet waves to make pictures of this inside of the body, in this case the head
Treatment
The goals of treatment are to:
- Reduce production of GH to normal levels
- Stop and reverse the symptoms caused by over-secretion of GH
Treatment may include:
Surgery – surgical removal of the pituitary or other tumor that is believed to be causing acromegaly. In most cases, this is the preferred treatment.
Radiosurgery – the use of highly focused external beams of radiation to shrink the tumor. Used most often in patients who do not respond to conventional surgery or medications.
Medication – drugs may be given to reduce the level of GH secretion from the pituitary gland. These include:
- Cabergoline (Dostinex) – given orally
- Octreotide (Sandostatin) – given by injections
Medications must often be combined with other therapies to treat larger tumors affecting surrounding structures.
Prevention
There are no guidelines for preventing acromegaly. Early diagnosis and treatment, however, will help prevent serious complications, some of which are irreversible.
Organizations
American Academy of Family Physicians
http://www.aafp.org
Pituitary Network Association
http://www.pituitary.org
National Institute of Diabetes & Digestive & Kidney Diseases
http://www.niddk.nih.gov
SOURCES:
American Academy of Family Physicians
National Institute of Diabetes & Digestive & Kidney Diseases
The Merck Manual of Medical Information. Simon and Schuster, Inc., 2000.
Last reviewed June 2002 by Medical Review Board
