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原发性醛固酮增多症与肾动脉狭窄并存。

Concurrence of primary aldosteronism and renal artery stenosis.

作者信息

Stokes G S, Monaghan J C, Roche J, Grunstein H, Gordon R D

机构信息

Hypertension Unit, Royal North Shore Hospital, St Leonards, New South Wales, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1992 May;19(5):300-3. doi: 10.1111/j.1440-1681.1992.tb00457.x.

Abstract
  1. An unusual clinical case is described in which renal artery stenosis (RAS) was found to coexist with adrenocortical hyperplasia, resulting in hypertension. 2. Partial relief of the hypertension was achieved by correction of RAS, and then further relief by extirpation of one adrenal gland affected by unilateral hyperplasia, in interventions 8 months apart. 3. Biochemical features typical of primary hyperaldosteronism were observed both before and after RAS repair but were not present after unilateral adrenalectomy. 4. The association of these two lesions could have occurred by chance, through genetic linkage, or by progression from RAS to tertiary aldosteronism.
摘要
  1. 本文描述了一例罕见的临床病例,其中发现肾动脉狭窄(RAS)与肾上腺皮质增生并存,导致高血压。2. 通过纠正RAS实现了高血压的部分缓解,然后在间隔8个月的两次干预中,通过切除单侧增生的一个肾上腺实现了进一步缓解。3. 在RAS修复前后均观察到原发性醛固酮增多症的典型生化特征,但单侧肾上腺切除术后这些特征消失。4. 这两种病变的关联可能是偶然发生的,通过基因连锁,或者是从RAS进展为三发性醛固酮增多症。

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