Diagnosis Acromegaly and hyperprolactinemia caused by a mixed-cell adenoma, secreting growth hormone and prolactin. Management Trans-sphenoidal surgery followed by medical therapy with 20 mg ...

In 95% of cases, acromegaly is caused by excessive growth hormone secretion from a pituitary adenoma, and is rarely the result of secretion of growth-hormone-releasing hormone or growth hormone ...

Patients with acromegaly make too much growth hormone, which causes them to grow disproportionately large bones, organs and ...

Acromegaly is a rare condition that happens when the pituitary gland produces too much growth hormone, usually as the result of a tumor inside the gland. Symptoms, which take time to develop ...

Pituitary adenomas account for about 15% of ... Mazziotti G, Torri V, Spinello M, Floriani I, Melmed S. Meta-analysis on the effects of octreotide on tumor mass in acromegaly. PLoS One 2012;7(5 ...

Sometimes, it's possible to cure acromegaly by removing the pituitary tumor that's causing it. Even if your acromegaly can't be cured, your symptoms should improve with treatment.

Pituitary adenomas are tiny lumps which grow within the pituitary gland. These can cause problems by producing extra hormones, for example growth hormone resulting in acromegaly, by preventing the ...

Only nine cases of acromegaly caused by pituitary carcinoma have been reported. 1 We describe a 47-year-old woman who presented in July 1996 with the features of acromegaly and an elevated mean ...

Acromegaly is caused due to prolonged overproduction of GH. 90% of the cases are due to benign tumor in the pituitary gland and rest of the cases are due to tumors in liver and other adrenal glands.

Pituitary gland tumors aren’t usually cancer, ... Drugs can also be helpful on tumors that make growth hormone, and in managing Cushing’s syndrome and acromegaly. Sources Update History.

Rarely, acromegaly can happen due to other reasons than a pituitary adenoma. For example, tumors in the lungs, adrenal glands, and pancreas may cause acromegaly.