Primary aldosteronism: difference in clinical presentation and long-term follow-up between adenoma and bilateral hyperplasia of the adrenal glands.

T Jeck, B Weisser, T Mengden, L Erdmenger, S Grüne, W Vetter
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引用次数: 21

Abstract

Since 1974 primary aldosteronism has been diagnosed in 71 patients in our outpatient clinic. Thirty-four patients had a unilateral aldosterone-producing adenoma, whereas bilateral adrenal hyperplasia was diagnosed in 37 patients. Although at the time of diagnosis the mean potassium values were lower and mean aldosterone levels were higher in patients with an adenoma, as compared to those with bilateral hyperplasia, these laboratory data did not allow us to differentiate between the two leading causes of primary aldosteronism in the individual patient due to pronounced overlap of laboratory values between the two groups. During the first few years, a successful differential diagnosis was made by adrenal phlebography and separate sampling of plasma aldosterone in both adrenal veins; later non-invasive imaging techniques such as computed tomography and radionuclide scanning were used. The best results were obtained in patients with adenoma who underwent adrenalectomy. Fifty-six percent of these patients were clinically and biochemically cured; 28% were improved and had normal blood pressure values during drug treatment. In contrast, patients with bilateral hyperplasia were treated pharmacologically, but only in half of the patients could normal blood pressure values be achieved. Two thirds of the male patients developed gynecomastia during spironolactone treatment. As expected, unilateral adrenalectomy was unsuccessful in the 7 patients with bilateral hyperplasia who underwent surgery. Our results confirm that surgical treatment of adrenal adenomas and drug treatment of bilateral hyperplasias are the appropriate therapy in primary aldosteronism. A differential diagnosis cannot be made on the basis of clinical and non-invasive laboratory data alone; imaging techniques have to be included in the diagnostic process.(ABSTRACT TRUNCATED AT 250 WORDS)

原发性醛固酮增多症:肾上腺腺瘤和双侧肾上腺增生的临床表现和长期随访的差异。
自1974年以来,在我们的门诊诊断出71例原发性醛固酮增多症。34例患者单侧醛固酮分泌腺瘤,37例诊断为双侧肾上腺增生。虽然在诊断时,与双侧增生患者相比,腺瘤患者的平均钾值较低,平均醛固酮水平较高,但这些实验室数据并不能使我们区分个体患者原发性醛固酮增多症的两个主要原因,因为两组之间的实验室值明显重叠。在最初的几年里,通过肾上腺静脉造影术和在肾上腺静脉中单独取样血浆醛固酮,成功地进行了鉴别诊断;后来使用了非侵入性成像技术,如计算机断层扫描和放射性核素扫描。腺瘤患者行肾上腺切除术效果最好。其中56%的患者经临床和生化治疗治愈;28%的患者在药物治疗期间血压有所改善并恢复正常。相比之下,双侧增生患者进行了药物治疗,但只有一半的患者可以达到正常的血压值。三分之二的男性患者在螺内酯治疗期间发生了男性乳房发育。正如预期的那样,7例接受手术的双侧肾上腺增生患者单侧肾上腺切除术失败。我们的结果证实手术治疗肾上腺腺瘤和药物治疗双侧增生是原发性醛固酮增多症的适当治疗方法。不能仅根据临床和非侵入性实验室数据作出鉴别诊断;成像技术必须包括在诊断过程中。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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