Primary hyperaldosteronism classification

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Eiman Ghaffarpasand, M.D. [2]

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Overview

Primary hyperaldosteronism may be classified into five groups, including adrenal carcinoma, familial hyperaldosteronism type I and II, Idiopathic hyperaldosteronism (IH), primary adrenal hyperplasia, and aldosterone producing adenoma (APA), which is either renin-responsive or renin-unresponsive.

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References

  1. Plouin, P.-F.; Amar, L.; Chatellier, G. (2004). "Trends in the prevalence of primary aldosteronism, aldosterone-producing adenomas, and surgically correctable aldosterone-dependent hypertension". Nephrology Dialysis Transplantation. 19 (4): 774–777. doi:10.1093/ndt/gfh112. ISSN 0931-0509.
  2. Gordon, R.D. (1994). "Mineralocorticoid hypertension". The Lancet. 344 (8917): 240–243. doi:10.1016/S0140-6736(94)93003-1. ISSN 0140-6736.
  3. Phillips, John L.; Walther, McClellan M.; Pezzullo, John C.; Rayford, Walter; Choyke, Peter L.; Berman, Arlene A.; Linehan, W. Marston; Doppman, John L.; Gill Jr., John R. (2000). "Predictive Value of Preoperative Tests in Discriminating Bilateral Adrenal Hyperplasia from an Aldosterone-Producing Adrenal Adenoma". The Journal of Clinical Endocrinology & Metabolism. 85 (12): 4526–4533. doi:10.1210/jcem.85.12.7086. ISSN 0021-972X.

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