Acromegaly
- PMID: 28613738
- Bookshelf ID: NBK431086
Acromegaly
Excerpt
Acromegaly is a rare disorder caused by excessive growth hormone production (GH), most commonly from an adenoma of the anterior pituitary gland. The resulting production of insulin-like growth factor 1 (IGF-1) causes the characteristic overgrowth of certain tissues resulting in coarsening of facial features, enlarging hands and feet, as well as effects on multiple systems throughout the body, including cardiovascular, rheumatologic, neurologic, pulmonary, neoplastic, and metabolic (see Image. Acromegaly, gigantism). Appropriate screening and early diagnosis are important to hinder associated morbidity and mortality related to the disease by treating early and the involvement of a multidisciplinary team.
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References
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- Drewes AM, Arlien-Søborg MC, Lunde Jørgensen JO, Jensen MP. [Acromegaly and symptoms of the motor apparatus]. Ugeskr Laeger. 2018 Nov 12;180(46) - PubMed
-
- Postma MR, Wolters TLC, van den Berg G, van Herwaarden AE, Muller Kobold AC, Sluiter WJ, Wagenmakers MA, van den Bergh ACM, Wolffenbuttel BHR, Hermus ARMM, Netea-Maier RT, van Beek AP. Postoperative use of somatostatin analogs and mortality in patients with acromegaly. Eur J Endocrinol. 2019 Jan 01;180(1):1-9. - PubMed
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- Vilar L, Vilar CF, Lyra R, Lyra R, Naves LA. Acromegaly: clinical features at diagnosis. Pituitary. 2017 Feb;20(1):22-32. - PubMed
-
- Vallar L, Spada A, Giannattasio G. Altered Gs and adenylate cyclase activity in human GH-secreting pituitary adenomas. Nature. 1987 Dec 10-16;330(6148):566-8. - PubMed
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