- A Case of AVP Dependent Bilateral Macronodular Adrenal Hyperplasia.
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Hyun Jin Kim, 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
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J Korean Endocr Soc. 2002;17(4):603-609. Published online August 1, 2002
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- 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.
- Gonadotropin-releasing hormone(GnRH) therapy in male patients with hypothalamic hypogonadism.
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Seog Won Park, Yoon Sok Chung, Choon Hee Chung, Sung Eun Kim, Eun Jig Lee, Hyun Chul Lee, Kap Bum Huh, Hyung Ki Choi, Moo Sang Lee, Ki Hyun Park
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J Korean Endocr Soc. 1993;8(1):27-34. Published online January 1, 2001
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- No abstract available.
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