医学
醛固酮
甾体11β-羟化酶
原发性醛固酮增多症
内分泌学
内科学
醛固酮增多症
低钾血症
盐皮质激素
醛固酮合酶
糖皮质激素
继发性高血压
皮质酮
肾素-血管紧张素系统
激素
血压
类固醇
作者
Hsieh Ching Cj,Wang Pw,Liu Jc,Tung Sc,Chien Wy,Lu Y,M-C. Kuo
出处
期刊:PubMed
[National Institutes of Health]
日期:1997-03-01
卷期号:20 (1): 52-7
被引量:4
摘要
Glucocorticoid remediable aldosteronism (GRA) is a hereditary cause of mineralocorticoid hypertension. The most common presentation is asymptomatic hypertension. Hypokalemia, hyperaldosteronism and suppressed plasma renin activity are other forms of primary hyperaldosteronism. However, the aldosterone secretion in these patients is regulated by adrenocortico-tropic hormone (ACTH) rather than the reninangiotension system. Here, we report a patient with a 12-year history of hypertension without response to any treatment until dexamethasone was administered. The diagnosis of GRA was confirmed by elevated plasma level of 18-oxocortisol, which is a unique steroid biochemical abnormality of this disease. In GRA, hybrid steroids (18-oxocortisol and 18-hydroxycortisol) are synthesized at the C-18 carbon of cortisol in a similar way as when corticosterone is converted to aldosterone. The gene duplication defect is on chromosome 8 codes for a chimerical 11 beta-hydroxylase/aldosterone synthase enzyme, causing ectopic expression of aldosterone synthase in zona fasiculata. Because this hypertension is remediable by exogenous glucocorticoid, this case was reported to raise attention about treatable aldosteronism.
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