A Case of AVP Dependent Bilateral Macronodular Adrenal Hyperplasia.
- Author:
Hyun Jin KIM
1
;
Se Hwa KIM
;
Yu Mie RHEE
;
Sung Eun KIM
;
Chul Woo AHN
;
Bong Soo CHA
;
Kyung Rae KIM
;
Hyun Chul LEE
;
Kap Bum HUH
;
Sung Kil LIM
Author Information
1. Department of Internal Medicine, Yonsei University, College of Medicine, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
ACTH independent bilateral macronodular adrenal hyperplasia;
Cushing's syndrome;
AVP stimulation test
- MeSH:
Adrenergic beta-Agonists;
Adrenocorticotropic Hormone;
Cushing Syndrome;
Female;
Gastric Inhibitory Polypeptide;
Humans;
Hydrocortisone;
Hyperplasia*;
Immunoglobulins;
Middle Aged;
Plasma;
Vasopressins
- From:Journal of Korean Society of Endocrinology
2002;17(4):603-609
- CountryRepublic of Korea
- Language:Korean
-
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, beta-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.
