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A case of primary aldosteronism combined with acquired nephrogenic diabetes insipidus

Authors
Kim K.Lee J.H.Kim S.C.Cha D.R.Kang Y.S.
Issue Date
2014
Publisher
Elsevier
Keywords
Aquaporin; Diabetes insipidus; Hyperaldosteronism; Hypokalemia
Citation
Kidney Research and Clinical Practice, v.33, no.4, pp 229 - 233
Pages
5
Indexed
SCOPUS
KCI
Journal Title
Kidney Research and Clinical Practice
Volume
33
Number
4
Start Page
229
End Page
233
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/9861
DOI
10.1016/j.krcp.2014.09.001
ISSN
2211-9132
2211-9140
Abstract
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. © 2014. The Korean Society of Nephrology. Published by Elsevier. All rights reserved.
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Kang, Young Sun
Ansan Hospital (Department of Nephrology and Hypertension, Ansan Hospital)
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