[2例原发性高醛固酮增多症]。

Vutreshni bolesti Pub Date : 1991-01-01
N Nakov, V Vladov, V Kolarski, K Dodev, R Rashkov
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引用次数: 0

摘要

本文报道两例女性原发性醛固酮增多症的临床病例。患者表现为动脉高血压、肌肉无力和感觉异常。发现严重的低钾血症对静脉输注钾有耐药性,但在3-4天内使用每日低剂量(100-200毫克)的一种醛缩酮拮抗剂螺缩酮成功治疗。其中一名患者的原发性醛固酮增多症与恶性皮质瘤细胞分泌醛固酮有关,经组织学证实。一次成功的手术使病人完全康复。另一位患者是由双侧肾上皮质增生引起的原发性醛固酮增多症的特发性形式。指出了原发性高醛固酮增多症的当代诊断和治疗可能性,以及动脉高血压患者血清钾水平和钾尿检查对及时成功诊断和治疗原发性高醛固酮增多症的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[2 cases of primary hyperaldosteronism].

Two clinical cases of women with primary hyperaldosteronism are reported. The patients presented with arterial hypertension, muscular weakness and paresthesia. Severe hypokalemia was found which was resistant to intravenous infusions of potassium but was successfully treated with low daily doses (100-200 mg) of spironolacton, an aldacton antagonist, in the course of 3-4 days. In one of the patients the primary hyperaldosteronism was related to aldosterone secretion by the cells of a malignant corticosteroma, proved histologically. A successful operation led to full recovery of the patient. In the other patient there was an idiopathic form of primary hyper aldosteronism caused by bilateral hyperplasia of the suprarenal cortex. Contemporary diagnostic and therapeutic possibilities in primary hyperaldosteronism as well as the importance of the examination of potassium serum level and kaliuria in the patients with arterial hypertension for the timely and successful diagnosis and treatment of primary hyperaldosteronism are pointed out.

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