What will happen to a person with excessive secretion of growth hormones from the pituitary gland

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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, and adults develop deformed bones but do not grow taller.

  • Heart failure, weakness, and vision problems are common.

  • The diagnosis is based on blood tests and imaging of the skull and hands.

  • Computed tomography (CT) or magnetic resonance imaging (MRI) of the head 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.

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 thus cannot increase the length of bones but it does cause acromegaly, in which the bones become deformed rather than elongated. Because changes occur slowly, they are usually not recognized for years.

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.

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.

  • Blood tests

  • Imaging tests

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.

Imaging of 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.

  • Surgery

  • Radiation therapy

  • Drug therapy

Stopping or reducing the overproduction of growth hormone is not easy. Doctors may need to use a combination of surgery, radiation therapy, and drug therapy.

Surgery to remove the pituitary tumor 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 cure the disorder. Long-term drug therapy is often needed after surgery. Radiation therapy is sometimes used as a follow-up treatment, particularly if a substantial amount of the tumor remains after surgery and acromegaly symptoms persist despite other treatments.

Drugs can also be used to treat elevated growth hormone levels. Drugs that act on the tumor to suppress growth hormone secretion and drugs that block growth hormone from interacting with its receptor are available. Both types of drugs reduce symptoms related to excessive growth hormone secretion.

The choice of drug is individualized to the person being treated, but most people receive treatment with a class of drugs called somatostatin receptor ligands, which reduce growth hormone secretion, thereby reducing IGF-1 production. In many cases, these drugs also shrink the tumor. These drugs include octreotide, lanreotide, and pasireotide. Each are usually given once a month.

Pegvisomant, a growth hormone receptor blocker, is also used to treat acromegaly. It lowers IGF-1 production by interfering with the growth hormone coming from the tumor. It is given as a daily injection under the skin and is effective in most people when the dose is increased to adequate levels. Occasionally, cabergoline is used to treat acromegaly, especially in milder cases when the serum IGF-1 level is not very elevated above normal. This drug is not as effective as somatostatin receptor ligands, but because it is taken by mouth rather than injection, it may be preferred by some people.

Several newer growth hormone blocker drugs, such as pegvisomant,may be useful for people who do not respond to somatostatin-type drugs. All of these drugs are effective in controlling acromegaly in many people as long as they continue to be taken; however, they do not provide a cure.

Radiation therapy Radiation Therapy for Cancer Radiation is a form of intense energy generated by a radioactive substance, such as cobalt, or by specialized equipment, such as an atomic particle (linear) accelerator. Radiation preferentially... read more involves the delivery of single or multiple smaller doses of radiation to the tumor, which is less traumatic than surgery. However, it may take several years for radiation to have its full effect on reducing growth hormone secretion. Later on, radiation therapy often results in deficiencies of other pituitary hormones because normal tissue is often also affected. Stereotactic radiation therapy, in which the radiation comes from several different directions (so it does not always go through the same normal tissue), has been developed for use with multiple types of radiation used including linear accelerators, proton beam, and gamma knife.

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What will happen to a person with excessive secretion of growth hormones from the pituitary gland

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What will happen to a person with excessive secretion of growth hormones from the pituitary gland

What will happen to a person with too much secretion of growth hormones from the pituitary gland Brainly?

In adults, excessive growth hormone for a long period of time produces a condition known as acromegaly, in which patients have swelling of the hands and feet and altered facial features. These patients also have organ enlargement and serious functional disorders such as high blood pressure, diabetes and heart disease.

What happens when someone produces too much growth hormone?

Acromegaly is a rare condition where the body produces too much growth hormone, causing body tissues and bones to grow more quickly. Over time, this leads to abnormally large hands and feet, and a wide range of other symptoms. Acromegaly is usually diagnosed in adults aged 30 to 50, but it can affect people of any age.

What happens if there is over or under secretion of growth hormone?

What happens if I have too little growth hormone? Too little growth hormone (deficiency) results in poor growth in children. In adults, it causes a reduced sense of wellbeing, increased fat, increased risk of heart disease and weak heart, muscles and bones.

What happens when there is too little secretion of growth hormones by the pituitary gland resulting to stunted growth?

Growth hormone deficiency (GHD), also known as dwarfism or pituitary dwarfism, is a condition caused by insufficient amounts of growth hormone in the body. Children with GHD have abnormally short stature with normal body proportions. GHD can be present at birth (congenital) or develop later (acquired).