Primary aldosteronism in a patient with familial adenomatous polyposis

被引：13

作者：

Alexander, GL

Thompson, GB

Schwartz, DA

机构：

[1] Mayo Clin & Mayo Fdn, Div Gastroenterol & Hepatol & Internal Med, Rochester, MN 55905 USA

[2] Mayo Clin & Mayo Fdn, Dept Surg, Rochester, MN 55905 USA

来源：

MAYO CLINIC PROCEEDINGS | 2000年 / 75卷 / 06期

关键词：

D O I：

10.4065/75.6.636

中图分类号：

R5 [内科学];

学科分类号：

1002 [临床医学]; 100201 [内科学];

摘要：

Patients with familial adenomatous polyposis (FAP) frequently have extracolonic manifestations of their disease, Prior reports have indicated an increased prevalence of adrenal lesions in patients with FAP. Although most of the adrenal lesions represent nonfunctioning adenomas, some patients have had hypercortisolism due to adrenocortical carcinoma or bilateral nodular hyperplasia, We present a case of patient with FAP who had mineralocorticoid excess due to an aldosterone-producing adrenocortical adenoma.

引用

页码：636 / 637

页数：2

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