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A case of primary aldosteronism combined with acquired nephrogenic diabetes insipidus

机译:原发性醛固酮增多症合并获得性肾病性尿崩症1例

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Aldosterone-producing adrenal adenoma can induce various clinical manifestations as a result of chronic exposure to aldosterone. We report a rare case of a 37-year-old man who complained of general weakness and polyuria. He was diagnosed with aldosterone-producing adrenal adenoma and nephrogenic diabetes insipidus. Aldosterone enhances the secretion of potassium in the collecting duct, which can lead to hypokalemia. By contrast, nephrogenic diabetes insipidus, which manifests as polyuria and polydipsia, can occur in several clinical conditions such as acquired tubular disease and those attributed to toxins and congenital causes. Among them, hypokalemia can also damage tubular structures in response to vasopressin. The patient's urine output was >3 L/d and was diluted. Owing to the ineffectiveness of vasopressin, we eventually made a diagnosis of nephrogenic diabetes insipidus. Laparoscopic adrenalectomy and intraoperative kidney biopsy were subsequently performed. The pathologic finding of kidney biopsy revealed a decrease in aquaporin-2 on immunohistochemical stain.
机译:由于长期暴露于醛固酮,导致产生醛固酮的肾上腺腺瘤可诱发多种临床表现。我们报告了一个罕见的案例,该案例是一名37岁的男子抱怨全身无力和多尿。他被诊断出患有产生醛固酮的肾上腺腺瘤和尿崩症。醛固酮会增强钾在收集管中的分泌,这会导致低钾血症。相比之下,表现为多尿和多饮的肾原性尿崩症可在多种临床情况下发生,例如获得性肾小管疾病以及那些归因于毒素和先天性原因的疾病。其中,低钾血症也可对血管加压素作出反应而损害肾小管结构。患者的尿量> 3 L / d,并被稀释。由于加压素的无效性,我们最终对肾原性尿崩症进行了诊断。随后进行了腹腔镜肾上腺切除术和术中肾脏活检。肾脏活检的病理发现显示免疫组织化学染色显示aquaporin-2减少。

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