| Literature DB >> 28810583 |
Hiroyuki Hirai1,2, Makoto Kanno1, Tsuyoshi Watanabe1,3, Hiroaki Satoh1,4.
Abstract
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 m2, 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.Entities:
Keywords: adrenalectomy; autosomal dominant polycystic kidney disease; kidney dysfunction; primary aldosteronism
Year: 2017 PMID: 28810583 PMCID: PMC5525647 DOI: 10.3892/etm.2017.4588
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447