An Update on Pituitary Neuroendocrine Tumors Leading to Acromegaly and Gigantism

Volume: 10, Issue: 11, Pages: 2254 - 2254
Published: May 22, 2021
Abstract
An excess of growth hormone (GH) results in accelerated growth and in childhood, the clinical manifestation is gigantism. When GH excess has its onset after epiphyseal fusion at puberty, the overgrowth of soft tissue and bone results in acromegaly. Persistent GH excess in gigantism also causes acromegalic features that become evident in the adult years. The causes of GH excess are primarily lesions in the pituitary, which is the main source of...
Paper Details
Title
An Update on Pituitary Neuroendocrine Tumors Leading to Acromegaly and Gigantism
Published Date
May 22, 2021
Volume
10
Issue
11
Pages
2254 - 2254
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