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Review
. 2008 Mar;37(1):101-22, viii.
doi: 10.1016/j.ecl.2007.10.002.

Acromegaly

Affiliations
Review

Acromegaly

Anat Ben-Shlomo et al. Endocrinol Metab Clin North Am. 2008 Mar.

Abstract

Acromegaly is caused by growth hormone hypersecretion, mostly from a pituitary adenoma, driving insulin-like growth factor 1 overproduction. Manifestations include skeletal and soft tissue growth and deformities; and cardiac, respiratory, neuromuscular, endocrine, and metabolic complications. Increased morbidity and mortality require early and tight disease control. Surgery is the treatment of choice for microadenomas and well-defined intrasellar macroadenomas. Complete resection of large and invasive macroadenomas rarely is achieved; hence, their low rate of disease remission. Pharmacologic treatments, including long-acting somatostatin analogs, dopamine agonists, and growth hormone receptor antagonists, have assumed more importance in achieving biochemical and symptomatic disease control.

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Figures

Fig. 1
Fig. 1
Treatment approach to a patient with acromegaly. (Modified from Melmed S. Medical progress: acromegaly. N Engl J Med 2006;355(24):2558–73; with permission. Copyright © 2006, Massachusetts Medical Society. All rights reserved.)

References

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