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一名儿童出现罕见的低血浆肾素性高血压。

Unusual low plasma renin hypertension in a child.

作者信息

Sann L, Revol A, Zachmann M, Legrand J C, Bethenod M

出版信息

J Clin Endocrinol Metab. 1976 Aug;43(2):265-71. doi: 10.1210/jcem-43-2-265.

DOI:10.1210/jcem-43-2-265
PMID:181394
Abstract

A four-year-old girl with hypertension (140/60) and chronic hypokalemic alkalosis was studied to determine the origin of this clinical feature. High exchangeable sodium (56.7 meq/kg vs. 45-55 meq/kg in controls) was associated with a low plasma renin activity (6 ng/1/min vs. 26 +/- 3.1 in controls) and reduced aldosterone secretion rate (5.56 mug/day; normal: 50-150 mug per day)). A low corticosterone secretion rate (0.228 mg/day vs. 0.50-0.65 in controls) and urinary tetrahydrodeoxycorticosterone (0.007 mg/day vs. 0.03-0.09 mg/day in controls) were found. The basal secretion rate of cortisol was also low (1.80 mg/m2/day vs. 5.4-16.7 mg/m2/day in controls) in spite of normal plasma ACTH: 78 pg/ml. The normal increase of the cortisol secretion rate (from 1.80 to 65 mg/m2/day) after synthetic ACTH stimulation ruled out a 17 alpha hydroxylase deficiency. The low sweat Na/K ratio (0.25) and the good suppressing efficacy of dexamethasone and of the spironolactones on hypertension and on the hypokalemic alkalosis agreed with the hypersecretion of a mineralocorticoid. The secretion rate of 18 hydroxydeoxycorticosterone was high (91 mug/day/1.73 m2 vs. 40-80 mug per day and per 1.73 m2). As the mineralocorticoid potency of this steroid is weak, we speculate that it might be the precursor of a more potent but unknown mineralocorticoid which could influence the ACTH secretion.

摘要

对一名患有高血压(140/60)和慢性低钾性碱中毒的4岁女孩进行了研究,以确定这种临床特征的病因。可交换钠升高(56.7 meq/kg,而对照组为45 - 55 meq/kg)与血浆肾素活性降低(6 ng/1/min,而对照组为26 +/- 3.1)以及醛固酮分泌率降低(5.56 μg/天;正常:50 - 150 μg/天)相关。发现皮质酮分泌率降低(0.228 mg/天,而对照组为0.50 - 0.65)以及尿四氢脱氧皮质酮降低(0.007 mg/天,而对照组为0.03 - 0.09 mg/天)。尽管血浆促肾上腺皮质激素(ACTH)正常(78 pg/ml),但皮质醇的基础分泌率也较低(1.80 mg/m²/天,而对照组为5.4 - 16.7 mg/m²/天)。合成ACTH刺激后皮质醇分泌率正常升高(从1.80升至65 mg/m²/天)排除了17α羟化酶缺乏症。低汗钠/钾比值(0.25)以及地塞米松和螺内酯对高血压和低钾性碱中毒的良好抑制效果与盐皮质激素分泌过多一致。18-羟脱氧皮质酮的分泌率较高(91 μg/天/1.73 m²,而正常为每天每1.73 m² 40 - 80 μg)。由于这种类固醇的盐皮质激素活性较弱,我们推测它可能是一种更强效但未知的盐皮质激素的前体,后者可能影响ACTH的分泌。

相似文献

1
Unusual low plasma renin hypertension in a child.一名儿童出现罕见的低血浆肾素性高血压。
J Clin Endocrinol Metab. 1976 Aug;43(2):265-71. doi: 10.1210/jcem-43-2-265.
2
Mineralocorticoid hypertension in childhood.
Mayo Clin Proc. 1977 May;52(5):323-8.
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Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension.
J Clin Endocrinol Metab. 1977 May;44(5):924-33. doi: 10.1210/jcem-44-5-924.
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Response of several adrenal steroids to ACTH stimulation in essential hypertension.原发性高血压患者几种肾上腺类固醇对促肾上腺皮质激素刺激的反应。
J Clin Endocrinol Metab. 1977 Feb;44(2):264-72. doi: 10.1210/jcem-44-2-264.
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Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism.地塞米松可抑制性醛固酮增多症患者的肾上腺球状带功能。
J Clin Endocrinol Metab. 1981 Jul;53(1):158-64. doi: 10.1210/jcem-53-1-158.
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An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension.一例伴有恶性高血压的17α-羟化酶缺乏症尸检病例。
J Clin Endocrinol Metab. 1983 May;56(5):915-9. doi: 10.1210/jcem-56-5-915.
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17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family.
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Regulation of mineralocorticoid secretion by the superfused fetal monkey adrenal gland: lack of stimulation of aldosterone by ACTH.体外灌流的胎猴肾上腺对盐皮质激素分泌的调节:促肾上腺皮质激素对醛固酮无刺激作用。
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Low renin hypertension and the adrenal cortex.低肾素性高血压与肾上腺皮质
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Mineralocorticoid hypertension and hypokalemia.盐皮质激素性高血压和低钾血症。
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引用本文的文献

1
Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.儿童类固醇疾病:先天性肾上腺增生症和表观盐皮质激素过多症。
Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12790-7. doi: 10.1073/pnas.96.22.12790.
2
A genetic defect resulting in mild low-renin hypertension.一种导致轻度低肾素性高血压的基因缺陷。
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):10200-5. doi: 10.1073/pnas.95.17.10200.
3
Apparent mineralocorticoid excess syndromes.表观盐皮质激素过多综合征
J Endocrinol Invest. 1995 Jul-Aug;18(7):518-32. doi: 10.1007/BF03349763.
4
Evidence for cortisol as the mineralocorticoid in the syndrome of apparent mineralocorticoid excess.
J Endocrinol Invest. 1992 Jun;15(6):471-4. doi: 10.1007/BF03348778.