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This is a hormonal disorder that is rare and develops when the pituitary gland produces an excess of growth hormone, usually as a result of a non-cancerous – benign tumor.
Since acromegaly is fairly uncommon and the changes physically occur slowly, it often is not recognized immediately. Acromegaly also cause changes gradually in shape of the facial area, for instance a lower brow and jaw that are protruding, a nose that is enlarged, lips that are thickened, as well as widely spacing between teeth.
Severe snoring as well as frequent very short interruptions in breathing during the night (sleep apnea) due to swelling of tissue that blocks upper airway. If an individual notices any long-term changes in appearance or other symptoms that might be linked with this disease, contact the primary care physician. Acromegaly normally grows slowly and even individual family members might not notice initially the gradual physical changes that have occurred.
Hormone for growth plays a role in regeneration and growth of the bones that is very important in stimulating additional tissues by stimulating the liver to generate another hormone referred to as “insulin-like growth factor-I” or IGF-I.
Most cases of acromegaly are developed by a non-cancerous or benign tumor, or adenoma of the pituitary gland. In a small group of individuals, this disease is developed by cancerous or benign tumors in other areas of the body, for instance the pancreas, lungs or adrenal glands.
As a beginning step toward diagnosis, the physician will first take a complete history medically and also conducts a physical exam. Since growth hormone triggers the liver to produce IGF-1 – which is another growth hormone – then levels of IGF-1 in the blood are elevated nearly always when an individual has acromegaly.
The physician will also test the levels of growth hormone to have a confirmation that this individual has acromegaly.


After this disease has been diagnosed by lab testing of IGF-1 and growth hormone levels, the physician will more than likely recommend an MRI of the brain to pinpoint the location and size of any tumor. Physicians treat this disease caused by tumors that are benign of the pituitary gland with surgery, radiation and medications.
If acromegaly is caused by any tumor outside the pituitary gland, the physician will develop individualized treatment plans based on the location of the tumor as well as whether it is cancerous or benign. Since transsphenoidal surgery is fairly complex, it is important to find a surgeon who has experience in performing these procedures.
Removing any tumor surgically may effectively and quickly return hormone levels to normal as well as relieve any pressure on the tissues surround the pituitary gland. Physicians might decide to manage an individual acromegaly with drugs especially when the pituitary tumor is surgically unreachable or if the individual is at a high risk of complications from the surgery. The physician might recommend treatment with radiation if cells of tumors remain post-surgery and if medication is not effective in reducing the level of growth hormone. After treatment for this disease, individuals will need to be continually monitored by a physician in order to make certain that the pituitary gland is functioning correctly and that the symptoms are getting better. This website is for informational purposes only and Is not a substitute for medical advice, diagnosis or treatment. Thyroid is a small gland situated at the front of your neck, just below the larynx about the size of two joined cherries.
The thyroid gland releases 3 important hormones- Tri-iodothyronine (T3), Thyroxine (T4) and Calcitonin. If the thyroid gland secretes a little amount of Tri-iodothyronine and Thyroxine, then we will get cold or tired, our skin gets dried and we will put on weight.


If the thyroid sends out too much of T3 and T4 hormone, then it causes anxiety, sweaty and overactive and we will also lose weight. The amount of T3 and T4 send out by the thyroid depends on how much thyroid-stimulating hormone is sent to it from the pituitary gland. If the amount of T3 and T4 drops out in the blood, then the pituitary gland sends out extra thyroid stimulating hormone to tell the thyroid to produce more. This is a hormonal disorder that is rare and develops when the pituitary gland produces an excess of growth hormone, usually as a result of a non-cancerous a€“ benign tumor.
Hormone for growth plays a role in regeneration and growth of the bones that is very important in stimulating additional tissues by stimulating the liver to generate another hormone referred to as a€?insulin-like growth factor-Ia€? or IGF-I.
Since growth hormone triggers the liver to produce IGF-1 a€“ which is another growth hormone a€“ then levels of IGF-1 in the blood are elevated nearly always when an individual has acromegaly. If you are new here, you might want to subscribe to the RSS feed for updates on this topic. It is controlled by the pituitary gland, which is the master gland for all other glands and hormones in our body. These hormones play a prominent role in controlling the entire body’s metabolism rate by circulating into the blood and stimulating cells to convert more glucose. Over iodine intake leads to increased secretion of hormones in thyroid gland which brings lot of disorders in the metabolism rate.



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