Gigantism (patient information): Difference between revisions
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Radiation has also been linked to learning disabilities, obesity, and emotional changes in children. Most experts will use radiation only if surgery and medication fail. | Radiation has also been linked to learning disabilities, obesity, and emotional changes in children. Most experts will use radiation only if surgery and medication fail. | ||
==What to expect (Outlook/Prognosis)?== | ==What to expect (Outlook/Prognosis)?== | ||
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Latest revision as of 15:12, 19 September 2012
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Gigantism |
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Gigantism On the Web |
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For the WikiDoc page on this topic, click here
Overview
Gigantism is abnormally large growth due to an excess of growth hormone during childhood, before the bone growth plates have closed.
What are the symptoms of Gigantism?
The child will grow in height, as well as in the muscles and organs. This excessive growth makes the child extremely large for his or her age.
Other symptoms include:
- Delayed puberty
- Double vision or difficulty with side (peripheral) vision
- Frontal bossing and a prominent jaw
- Headache
- Increased sweating
- Irregular periods (menstruation)
- Large hands and feet with thick fingers and toes
- Release of breast milk
- Thickening of the facial features
- Weakness
What causes Gigantism?
The most common cause of too much growth hormone release is a noncancerous (benign) tumor of the pituitary gland. Other causes include:
- Carney complex
- McCune-Albright syndrome (MAS)
- Multiple endocrine neoplasia type 1 (MEN-1)
- Neurofibromatosis
If excess growth hormone occurs after normal bone growth has stopped, the condition is known as acromegaly.
Gigantism is very rare.
Diagnosis
- CT or MRI scan of the head showing pituitary tumor
- Failure to suppress serum growth hormone (GH) levels after an oral glucose challenge (maximum 75g)
- High prolactin levels
- Increased insulin growth factor-I (IGF-I) levels
Damage to the pituitary may lead to low levels of other hormones, including:
- Cortisol
- Estradiol(girls)
- Testosterone (boys)
- Thyroid hormone
When to seek urgent medical care?
Call your health care provider if your child has signs of excessive growth.
Treatment options
In pituitary tumors with well-defined borders, surgery is the treatment of choice and can cure many cases.
For situations in which surgery cannot completely remove the tumor, medication is the treatment of choice. The most effective medications are somatostatin analogs (such as octreotide or long-acting lanreotide), which reduce growth hormone release.
Dopamine agonists (bromocriptine mesylate, cabergoline) have also been used to reduce growth hormone release, but these are generally less effective. Pegvisomant, a medication that blocks the effect of growth hormone, may be used.
Radiation therapy has also been used to bring growth hormone levels to normal. However, it can take 5 - 10 years for the full effects to be seen and this almost always leads to low levels of other pituitary hormones.
Radiation has also been linked to learning disabilities, obesity, and emotional changes in children. Most experts will use radiation only if surgery and medication fail.
What to expect (Outlook/Prognosis)?
Pituitary surgery is usually successful in limiting growth hormone production.
Possible complications
Surgery and radiation can both lead to low levels of other pituitary hormones, which can cause: