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原发性醛固酮增多症包括原发性肾上腺增生和腺瘤。

Primary aldosteronism is comprised of primary adrenal hyperplasia and adenoma.

作者信息

Biglieri E G, Kater C E, Arteaga E E

出版信息

J Hypertens Suppl. 1984 Dec;2(3):S259-61.

PMID:6599673
Abstract

Primary aldosteronism due to primary adrenal hyperplasia (PAH) is described. Hypertension, hypokalaemia, hyperaldosteronism and renin suppression were corrected by unilateral adrenalectomy in 3/5 patients and by spironolactone treatment in 2/5. Blood pressure and hormonal parameters have remained normal for up to seven years after surgery and spironolactone management. Four patients had bilateral micro- and macronodular hyperplasia and one had unilateral hyperplasia. While hormonally and biochemically identical to patients with aldosterone producing adenoma, PAH can be distinguished from idiopathic hyperaldosteronism (adrenal hyperplasia). The inability to demonstrate a tumour by computed tomography but the presence of bilateral elevations of aldosterone concentration in adrenal venous blood identifies PAH.

摘要

本文描述了原发性肾上腺增生所致的原发性醛固酮增多症(PAH)。3/5的患者通过单侧肾上腺切除术纠正了高血压、低钾血症、醛固酮增多症和肾素抑制,2/5的患者通过螺内酯治疗得到纠正。术后及螺内酯治疗后长达7年,血压和激素参数一直保持正常。4例患者有双侧微小结节性增生,1例有单侧增生。虽然PAH在激素和生化方面与醛固酮瘤患者相同,但可与特发性醛固酮增多症(肾上腺增生)相鉴别。计算机断层扫描未能显示肿瘤,但肾上腺静脉血中醛固酮浓度双侧升高可确诊PAH。

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