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==Overview==
==Overview==
Common causes of primary hyperaldosteronism include aldosterone-secreting adenoma, bilateral hyperplasia of the adrenal glands and ectopic secretion of aldosterone from ovaries and kidneys. Less common causes of primary hyperaldosteronism include familial hyperaldosteronism types I-III, pure aldosterone-producing adrenocortical carcinomas and unilateral hyperplasia of the adrenal gland.
==Causes==
==Causes==
=== Common Causes ===
=== Common Causes ===

Revision as of 19:29, 19 July 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Syed Hassan A. Kazmi BSc, MD [2]

Overview

Common causes of primary hyperaldosteronism include aldosterone-secreting adenoma, bilateral hyperplasia of the adrenal glands and ectopic secretion of aldosterone from ovaries and kidneys. Less common causes of primary hyperaldosteronism include familial hyperaldosteronism types I-III, pure aldosterone-producing adrenocortical carcinomas and unilateral hyperplasia of the adrenal gland.

Causes

Common Causes

Common causes of Conn's Syndrome may be divided into:

  • Adrenal causes:
    • Aldosterone-secreting adrenal adenoma (APA-benign tumor, 50-60%)
    • Idiopathic hyperaldosteronism (IHA-Bilateral hyperplasia of the adrenal gland, 40-50%)
  • Extra-adrenal causes
    • Ectopic secretion of aldosterone (Ovaries and Kidneys)

Less Common Causes

  • Familial hyperaldosteronism type I (glucocorticoid-remediable aldosteronism [GRA])
  • Familial hyperaldosteronism II (the familial occurrence of APA or bilateral idiopathic hyperplasia or both)
  • Familial hyperaldosteronism type III (associated with the germline mutation in the KCNJ5 potassium channel)
  • Pure aldosterone-producing adrenocortical carcinomas
  • Unilateral adrenal hyperplasia


References

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