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Characteristics of Acromegaly in Korea with a Literature Review

Acromegaly is a slowly progressive disease caused by excessive growth hormone (GH), which is related to a GH secreting pituitary tumor in most cases. Herein, we describe the epidemiology, clinical characteristics, and treatment of acromegaly in Korea with a literature review. The average annual inci...

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Detalles Bibliográficos
Autores principales: Hong, Jae Won, Ku, Cheol Ryong, Kim, Sun Ho, Lee, Eun Jig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3811698/
https://www.ncbi.nlm.nih.gov/pubmed/24396674
http://dx.doi.org/10.3803/EnM.2013.28.3.164
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author Hong, Jae Won
Ku, Cheol Ryong
Kim, Sun Ho
Lee, Eun Jig
author_facet Hong, Jae Won
Ku, Cheol Ryong
Kim, Sun Ho
Lee, Eun Jig
author_sort Hong, Jae Won
collection PubMed
description Acromegaly is a slowly progressive disease caused by excessive growth hormone (GH), which is related to a GH secreting pituitary tumor in most cases. Herein, we describe the epidemiology, clinical characteristics, and treatment of acromegaly in Korea with a literature review. The average annual incidence of acromegaly in Korea was 3.9 cases per million people, which was within the range of previous Western studies. The primary treatment for acromegaly was also transsphenoidal adenomectomy, which accounted for 90.4% of patients whose primary therapeutic options were known. The overall surgical remission rates were 89%, 87%, 64%, 70%, and 50% for modified Hardy classification I, II, IIIA, IIIB, and IV, respectively. An updated and larger study regarding the treatment outcome of medical/radiotherapy in Korean acromegalic patients is needed.
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spelling pubmed-38116982014-01-06 Characteristics of Acromegaly in Korea with a Literature Review Hong, Jae Won Ku, Cheol Ryong Kim, Sun Ho Lee, Eun Jig Endocrinol Metab (Seoul) Review Article Acromegaly is a slowly progressive disease caused by excessive growth hormone (GH), which is related to a GH secreting pituitary tumor in most cases. Herein, we describe the epidemiology, clinical characteristics, and treatment of acromegaly in Korea with a literature review. The average annual incidence of acromegaly in Korea was 3.9 cases per million people, which was within the range of previous Western studies. The primary treatment for acromegaly was also transsphenoidal adenomectomy, which accounted for 90.4% of patients whose primary therapeutic options were known. The overall surgical remission rates were 89%, 87%, 64%, 70%, and 50% for modified Hardy classification I, II, IIIA, IIIB, and IV, respectively. An updated and larger study regarding the treatment outcome of medical/radiotherapy in Korean acromegalic patients is needed. Korean Endocrine Society 2013-09 2013-09-13 /pmc/articles/PMC3811698/ /pubmed/24396674 http://dx.doi.org/10.3803/EnM.2013.28.3.164 Text en Copyright © 2013 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hong, Jae Won
Ku, Cheol Ryong
Kim, Sun Ho
Lee, Eun Jig
Characteristics of Acromegaly in Korea with a Literature Review
title Characteristics of Acromegaly in Korea with a Literature Review
title_full Characteristics of Acromegaly in Korea with a Literature Review
title_fullStr Characteristics of Acromegaly in Korea with a Literature Review
title_full_unstemmed Characteristics of Acromegaly in Korea with a Literature Review
title_short Characteristics of Acromegaly in Korea with a Literature Review
title_sort characteristics of acromegaly in korea with a literature review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3811698/
https://www.ncbi.nlm.nih.gov/pubmed/24396674
http://dx.doi.org/10.3803/EnM.2013.28.3.164
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