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首页> 外文期刊>Experimental and therapeutic medicine >Kidney dysfunction following adrenalectomy in autosomal dominant polycystic kidney disease complicated with primary aldosteronism: A case report
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Kidney dysfunction following adrenalectomy in autosomal dominant polycystic kidney disease complicated with primary aldosteronism: A case report

机译:肾功能紊乱后肾上腺切除术后常染色体显性多囊肾疾病,复杂的原发性醛固醛症:案例报告

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摘要

The present study reported a case of autosomal dominant polycystic kidney disease complicated with primary aldosteronism in a 49-year-old woman. The patient was referred for refractory hypertension. Laboratory examinations revealed low potassium and renin levels. Computed tomography indicated a right adrenal tumor and multiple renal cysts. Adrenal vein sampling revealed a high aldosterone level on the side of the tumor. The patient was diagnosed with autosomal dominant polycystic kidney disease complicated by primary aldosteronism and adrenalectomy was performed. Over the following 7 months, the estimated glomerular filtration rate decreased from 76 to 48 ml/min/ 1.73 m(2), which was attributed to glomerular hyperfiltration correction induced by hyperaldosteronism remission, indicating kidney dysfunction. Clinicians must therefore monitor for the unmasking of kidney dysfunction following adrenalectomy in such cases.
机译:本研究报告了一个49岁女性中对原发性醛固酮的常染色体显性多囊肾疾病的情况。 患者被称为难治性高血压。 实验室考试显示出低钾和肾素水平。 计算断层扫描表明右肾肿瘤和多种肾囊肿。 肾上腺静脉抽样揭示了肿瘤侧的高醛酮水平。 患者被诊断出患有常染色体显性的多囊肾疾病,并进行肾上腺切除术。 在接下来的7个月内,估计的肾小球过滤速率从76升至48ml / min / 1.73 m(2),这归因于甲状腺肿大缓解诱导的肾小球高滤育校正,表明肾功能紊乱。 因此,在这种情况下,临床医生必须监测肾上腺切除后肾功能紊乱的揭露。

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