产生原发性醛固酮增多症的异位肾上腺皮质腺瘤。 - Suppr | 超能文献

Heterotopic adrenocortical adenoma producing primary aldosteronism.

作者信息

Flanagan M J, McDonald J H

出版信息

J Urol. 1967 Aug;98(2):133-9. doi: 10.1016/S0022-5347(17)62839-8.

DOI:10.1016/S0022-5347(17)62839-8

Abstract

摘要

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Heterotopic adrenocortical adenoma producing primary aldosteronism.产生原发性醛固酮增多症的异位肾上腺皮质腺瘤。

J Urol. 1967 Aug;98(2):133-9. doi: 10.1016/S0022-5347(17)62839-8.

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Hyperaldosteronism due to adrenocortical adenoma and adenomatous hyperplasia.

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[An observation of Conn's syndrome. Clinical and biological study].

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Functional black adenoma of the adrenal cortex. A rare cause of primary aldosteronism.

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[Current problems in primary aldosteronism--4 cases of normokalemic primary aldosteronism (1st degree) caused by adenoma and 3 cases of aldosteronism, 1st degree, caused by hyperplasia (2 hypokalemic cases, a normokalemic case)].原发性醛固酮增多症的当前问题——4例由腺瘤引起的正常血钾性原发性醛固酮增多症（1级）和3例由增生引起的1级醛固酮增多症（2例低钾血症病例，1例正常血钾病例）

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Twenty-four year spironolactone therapy in an aged patient with aldosterone-producing adenoma.老年醛固酮瘤患者接受螺内酯治疗24年

Acta Endocrinol (Copenh). 1992 Feb;126(2):186-90. doi: 10.1530/acta.0.1260186.

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Primary aldosteronism due to adrenocortical adenoma (Conn's syndrome).

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[Idiopathic aldosteronism caused by bilateral adrenocortical hyperplasia].

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Clinical experience with aldosteronism. Report of two cases.

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[Normokalemic primary hyperaldosteronism].[正常血钾性原发性醛固酮增多症]

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引用本文的文献

1

Ectopic aldosteronoma associated to another adrenocortical adenoma in the adrenal gland of the same side.同侧肾上腺中与另一个肾上腺皮质腺瘤相关的异位醛固酮瘤。

J Endocrinol Invest. 1995 Nov;18(10):809-12. doi: 10.1007/BF03349816.

2

Primary aldosteronism: experience with current diagnostic criteria and surgical treatment in fourteen patients.原发性醛固酮增多症：14例患者采用现行诊断标准及手术治疗的经验

Ann Surg. 1968 May;167(5):718-27. doi: 10.1097/00000658-196805000-00010.

3

[Ectopic paraneoplastic endocrinopathies associated with water-electrolyte balance disorders].[与水电解质平衡紊乱相关的异位副肿瘤内分泌病]

Klin Wochenschr. 1973 Apr 15;51(8):361-76. doi: 10.1007/BF01468084.