Aldosterone deficiency after unilateral adrenalectomy for Conn's syndrome: a case report and literature review
- PMID: 25604311
- PMCID: PMC4336421
- DOI: 10.1016/j.ijscr.2015.01.013
Aldosterone deficiency after unilateral adrenalectomy for Conn's syndrome: a case report and literature review
Abstract
Introduction: Approximately 35% of cases of Conn's syndrome (primary aldosteronism) result from a solitary functioning adrenal adenoma, and these patients are best managed by adrenalectomy. Postoperative hypoaldosteronism after unilateral adrenalectomy is uncommon.
Case presentation: We present a case and literature review of hypoaldosteronism after unilateral adrenalectomy for Conn's syndrome, which demonstrates the insidious and sometimes delayed presentation.
Discussion: In this clinical case we summarize the previously published cases of post-adrenalectomy hypoaldosteronism based on a PUBMED and EBSCOhost search of all peer-reviewed publications (original articles and reviews) on this topic. A few cases of aldosterone insufficiency post-adrenalectomy for Conn's syndrome were identified. The etiological factors for prolonged selective suppression of aldosterone secretion after unilateral adrenalectomy remain unclear.
Conclusion: It is important to be aware of the risk of postoperative hypoaldosteronism in this patient population. Close postoperative follow-up is necessary and strongly recommended, especially in patients with certain risk factors. Patients may need mineralocorticoid supplementation during this period.
Keywords: Adrenalectomy; Aldosterone; Conn’s; Hypertension; Hypokalemia.
Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.
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