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AVP 자극검사 양성 양측성 거대결절성 부신피질 증식

Other Titles
 A Case of AVP Dependent Bilatera Macronodular Adrenal Hyperplasia 
Authors
 김현진  ;  김세화  ;  이유미  ;  안철우  ;  차봉수  ;  김경래  ;  이현철 
Citation
 Journal of Korea Society of Endocrinology (대한내분비학회지), Vol.17(4) : 603-609, 2002 
Journal Title
 Journal of Korea Society of Endocrinology (대한내분비학회지) 
ISSN
 1015-6380 
Issue Date
2002
Keywords
ACTH independent bilateral macronodular adrenal hyperplasia ; Cushing's syndrome ; AVP stimulation test
Abstract
Adrenocorticotropin(ACTH) independent bilateral macronodular adrenal hyperplasia(AIMAH) is a rare form of Cushing´s syndrome, in which unique endocrinological, clinical and histopathological features have been described. In AIMAH, cortisol secretion is autonomous and independent of ACTH, thus plasma ACTH levels are persistently suppressed. Various etiological mechanisms have been proposed to explain the development of AIMAH, the development of aberrant adrenal sensitivity to gastric inhibitory polypeptide(GIP), vasopressin, β-adrenergic receptor agonists or the presence of circulating adrenal stimulating immunoglobulins have been suggested. We report on a 46-year-old female who had Cushing´s syndrome, due to AIMAH, with a positive response to vasopressin
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Ahn, Chul Woo(안철우) ORCID logo https://orcid.org/0000-0003-3733-7486
Cha, Bong Soo(차봉수) ORCID logo https://orcid.org/0000-0003-0542-2854
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/143744
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