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Overproduction of growth hormone causes excessive growth. In children, the condition is called

gigantism. In adults, it is called acromegaly.

Excessive growth hormone is almost always caused by a noncancerous (benign)pituitary tumor.

Children develop great stature; adults develop deformed bones but do not growtaller.

Heart failure, weakness, and vision problems are common.

The diagnosis is based on blood tests and x-rays of the skull and hands.

Other imaging tests are done to look for the cause.

A combination of surgery, radiation therapy, and drug therapy is used to treat the

overproduction of growth hormone.

Growth hormone stimulates the growth of bones, muscles, and many internal organs. Excessive

growth hormone, therefore, leads to abnormally robust growth of all of these tissues.

Overproduction of growth hormone is almost always caused by a noncancerous (benign) pituitary

tumor (adenoma). Certain rare tumors of the pancreas and lungs also can produce hormones that

stimulate the pituitary to produce excessive amounts of growth hormone, with similar

consequences.

Symptoms

If excessive growth hormone production starts before the growth plates have closed (that is, in

children), the condition produces gigantism. The long bones grow enormously. A person grows to

unusually great stature, and the arms and legs lengthen. Puberty may be delayed, and the

genitals may not develop fully.

In most cases, excessive production of growth hormone begins between the ages of 30 and 50,

long after the growth plates of the bones have closed. Increased growth hormone in adults

Acromegaly and Gigantism

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produces acromegaly, in which the bones become deformed rather than elongated. Because

changes occur slowly, they are usually not recognized for years.

Did You Know?

A woman with acromegaly can

produce breast milk even if she is not

breastfeeding.

The person's facial features become coarse, and the hands and feet swell. Larger rings, gloves,

shoes, and hats are needed. Overgrowth of the jawbone (mandible) can cause the jaw to protrude

(prognathism). Cartilage in the voice box (larynx) may thicken, making the voice deep and husky.

The ribs may thicken, creating a barrel chest. Joint pain is common; after many years, crippling

degenerative arthritis may occur.

In both gigantism and acromegaly, the tongue may enlarge and become more furrowed. Coarse

body hair, which typically darkens, increases as the skin thickens. The sebaceous and sweat

glands in the skin enlarge, producing excessive perspiration and often an offensive body odor.

The heart usually enlarges, and its function may be so severely impaired that heart failure occurs.

Sometimes a person feels disturbing sensations and weakness in the arms and legs as enlarging

tissues compress the nerves. Nerves that carry messages from the eyes to the brain may also be

compressed, causing loss of vision, particularly in the outer visual fields. The pressure on the

brain may also cause severe headaches.

Nearly all women with acromegaly have irregular menstrual cycles. Some women produce breast

milk even though they are not breastfeeding (galactorrhea) because of either too much growth

hormone or a related increase in prolactin. About one third of men who have acromegaly develop

erectile dysfunction. There is also an increased likelihood of developing diabetes mellitus, high

blood pressure (hypertension), heart failure, sleep apnea, and certain tumors, particularly affecting

the large intestine, which may become cancerous. Life expectancy is reduced in people with

untreated acromegaly.

Diagnosis

In children, rapid growth may not seem abnormal at first. Eventually, however, the abnormality of

the extreme growth becomes clear.

In adults, because the changes induced by high levels of growth hormone occur slowly,

acromegaly often is not diagnosed until many years after the first symptoms appear. Serial

photographs (those taken over many years) may help a doctor establish the diagnosis. An x-ray of

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the skull may show thickening of the bones and enlargement of the nasal sinuses. X-rays of the

hands show thickening of the bones under the fingertips and swelling of the tissue around the

bones. Blood sugar levels and blood pressure may be high.

The diagnosis is confirmed by blood tests, which usually show high levels of both growth hormoneand insulin-like growth factor 1 (IGF-1). Because growth hormone is released in short bursts and

the levels of growth hormone often fluctuate dramatically even in people without acromegaly, a

single high level of growth hormone in the blood is insufficient to make the diagnosis. Doctors

must give something that would normally suppress growth hormone levels, most commonly a

glucose drink (the oral glucose tolerance test), and show that normal suppression does not occur.

This test is not necessary when the clinical features of acromegaly are obvious, the IGF-1 level is

high, or a tumor is seen in the pituitary on scanning.

A computed tomography (CT) or magnetic resonance imaging (MRI) scan is usually done to look

for abnormal growths in the pituitary gland. Because acromegaly is usually present for some years

before being diagnosed, a tumor is seen on these scans in most people.

Treatment

Stopping or reducing the overproduction of growth hormone is not easy; thus, doctors may need

to use a combination of surgery, radiation therapy, and drug therapy.

Surgery by an experienced surgeon is currently regarded as the best first treatment for most

people with acromegaly caused by a tumor. It results in an immediate reduction in tumor size and

growth hormone production, most often without causing deficiency of other pituitary hormones.

Unfortunately, tumors are often large by the time they are found, and surgery alone does not

usually produce a cure. Radiation therapy is often used as a follow-up treatment, particularly if a

substantial amount of the tumor remains after surgery and acromegaly persists.

Radiation therapy involves the use of supervoltage irradiation, which is less traumatic than

surgery. This treatment may take several years to have its full effect, however, and often results in

later deficiencies of other pituitary hormones, as normal tissue is often also affected. More

directed radiation therapy, such as stereotactic radiosurgery, is being tried to speed results and

spare the normal pituitary tissue.

Drug therapy can also be used to lower growth hormone levels. Occasionally,bromocriptine

and other drugs that act like dopamine are of some benefit. The most effective drugs, however,

are those that are forms of somatostatin, the hormone that normally blocks growth hormone

production and secretion. These drugs includeoctreotide

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and its newer long-acting analogs, which only have to be given about once a month. These drugs

are effective in controlling acromegaly in many people as long as they continue to be taken (they

do not provide a cure). Their use has been limited by the need to inject them and by their high

cost. This may change as such drugs become longer acting and more readily available. Several

new growth hormone blocker drugs, such aspegvisomant

, are now available and may be useful for people who do not respond to somatostatin-type drugs.