Masking by hypokalemia-primary aldosteronism with undetectable aldosterone

被引:1
|
作者
Boyle, Rebecca A. [1 ,2 ,3 ]
Baker, Jessica E. [4 ,5 ]
Charu, Vivek [6 ]
Rainey, William E. [4 ,5 ]
Bhalla, Vivek [1 ,2 ]
机构
[1] Stanford Univ, Dept Med, Stanford Hypertens Ctr, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Sch Med, Div Nephrol, Stanford, CA 94305 USA
[3] Stanford Hosp, Stanford HealthCare, Stanford, CA USA
[4] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Internal Med, Div Metab Endocrinol & Diabet, Ann Arbor, MI 48109 USA
[6] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
关键词
aldosterone; hypertension; hypokalemia; potassium channel; somatic mutation; ADENOMAS;
D O I
10.1093/ckj/sfaa150
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Primary aldosteronism is the most common cause of secondary hypertension; however, the dynamic regulation of aldosterone by potassium is less well studied and current diagnostic recommendations are imprecise. We describe a young man who presented with resistant hypertension and severe hypokalemia. The workup initially revealed undetectable aldosterone despite acute potassium repletion. Chronic potassium supplementation eventually uncovered hyperaldosteronism. In situ genetic studies revealed a gain-of-function KCNJ5 mutation within an aldosterone-producing adenoma that was clinically responsive to changes in extracellular potassium. We highlight a unique presentation of Conn's syndrome and discuss the implications for the molecular mechanisms of potassium regulation of aldosterone.
引用
收藏
页码:1269 / 1271
页数:3
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