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原发性醛固酮增多症患者的诊断方法。

Diagnostic approach to patients with primary hyperaldosteronism.

作者信息

Detollenaere M, Duprez D, Missault L, Rubens R, De Buyzere M, Vermeulen A, Clement D L

机构信息

Department of Cardiology and Angiology, University Hospital, Ghent, Belgium.

出版信息

Acta Clin Belg. 1991;46(2):100-5. doi: 10.1080/17843286.1991.11718150.

Abstract

We report the case of a 38-year-old patient with primary hyperaldosteronism. The diagnosis was made by the demonstration of a non-suppressible high aldosterone level in association with a hypokalemia, an inappropriate kaliuresis and low plasma renin activity. As the choice of the therapeutic approach is dictated by the subtype, further investigation was needed. Using a number of hormonal studies and noninvasive imaging techniques, we could establish the diagnosis of adrenocortical adenoma. Histological examination confirmed our diagnosis. We further discuss briefly the characteristics of the four subtypes of primary hyperaldosteronism and show that the used biochemical markers and imaging techniques are able to differentiate them.

摘要

我们报告了一例38岁的原发性醛固酮增多症患者。诊断依据是发现醛固酮水平持续升高且不可被抑制,同时伴有低钾血症、不适当的尿钾排泄增多以及血浆肾素活性降低。由于治疗方法的选择取决于亚型,因此需要进一步检查。通过一系列激素研究和非侵入性成像技术,我们得以确诊为肾上腺皮质腺瘤。组织学检查证实了我们的诊断。我们还简要讨论了原发性醛固酮增多症四种亚型的特点,并表明所使用的生化标志物和成像技术能够对它们进行区分。

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