Acromegaly is a disorder of the pituitary gland which produces excess growth hormones and thus results in excessive growth, first in the hands and feet, as soft tissue begins to swell.
Acromegaly is the Greek word for "extremities" and "enlargement." When the pituitary gland produces excess growth hormones, excessive abnormal growth occurs. This is called acromegaly. The excessive growth occurs first in the hands and feet, as soft tissue begins to swell. This rare disease affects mostly middle-aged adults. Untreated, the disease can lead to severe illness and death.
Overproduction of growth hormone (GH) by the pituitary gland over a long period of time causes acromegaly. There are several reasons for overproduction of GH. The most common reason is the presence of a pituitary adenoma, which is a benign (noncancerous) tumor of the pituitary gland. These tumors produce excess GH.
According to the National Institute of Diabetes and Digestive and Kidney Diseases, more than 95 percent of people with acromegaly have a pituitary adenoma.
Tumors outside the pituitary gland can also cause acromegaly, but this is rare.
Symptoms of acromegaly vary depending on how long the patient has had the disease. The following are the most common symptoms of acromegaly. However, each individual may experience symptoms differently. Symptoms may include:
Swelling of the hands and feet
Facial features become coarse as bones grow
Body hair becomes coarse as the skin thickens and/or darkens
Increased perspiration accompanied with body odor
Enlarged lip, nose, and tongue
Thickened ribs (creating a barrel chest)
Enlargement of other organs
Strange sensations and weakness in arms and legs
Fatigue and weakness
Loss of vision
Irregular menstrual cycles in women
Breast milk production in women
Impotence in men
The symptoms of acromegaly may resemble other conditions or medical problems. Always consult your doctor for a diagnosis.
Due to the subtlety of the symptoms, acromegaly is often not diagnosed until years later. In addition to a complete medical history and medical examination, diagnostic procedures for acromegaly may include:
Serial photos taken over the years (to observe physical changes in the patient)
X-rays (to detect bone thickening)
Blood tests (to check the growth hormone level)
MRI or CT scan, to detect tumors
Specific treatment for acromegaly will be determined by your doctor based on:
Your age, overall health, and medical history
Extent of the disease
Your tolerance for specific medications, procedures, or therapies
Expectations for the course of the disease
Your opinion or preference
Treatment of acromegaly depends on the cause of the disease. More than 95 percent of acromegaly cases are caused by benign tumors on the pituitary gland. Because the tumor is compressing the pituitary gland, the hormone production can be altered by removing or reducing the size of the tumor. Some other acromegaly cases are caused by tumors of the pancreas, lungs, or adrenal glands.
The goal of treatment is to restore the pituitary gland to normal function, producing normal levels of growth hormone.
Treatment may include surgical removal of the tumor, radiation therapy, and use of a growth hormone-blocking drug.
Left untreated, acromegaly can lead to cardiovascular problems, arthritis, diabetes mellitus and hypertension. The disease also increases a patient's risk for cardiovascular disease and colon polyps that may lead to cancer.
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