Unmasking Secondary Hypertension: Renal Artery Stenosis Concealing the Diagnosis of Primary Hyperaldosteronism

A 24-year-old woman with no prior comorbidities presented with severe, treatment-resistant hypertension characterized by episodic headaches and persistent systolic blood pressures above 140 mm Hg despite lifestyle modifications. Initial evaluation revealed hypokalemia and metabolic alkalosis with an aldosterone-to-renin ratio suggestive, but not diagnostic, of primary hyperaldosteronism. Secondary workup excluded pheochromocytoma, Cushing's syndrome, and thyroid disease. Imaging identified right renal artery fibromuscular dysplasia with angiographic narrowing of approximately 30%. Despite maximal medical therapy, her hypertension persisted, and repeat studies later demonstrated progression of stenosis to 70-75%, prompting angioplasty. The intervention improved arterial patency but failed to normalize her blood pressure or correct her tendency toward hypokalemia. Re-evaluation demonstrated a 1.7-cm left adrenal mass, and adrenal venous sampling confirmed unilateral aldosterone hypersecretion. The patient underwent laparoscopic adrenalectomy with pathology confirming an aldosterone-producing adenoma. Following surgery, she achieved normalization of potassium and sustained normotension without antihypertensive medications. This case highlights the diagnostic challenges when two secondary causes of hypertension coexist. Fibromuscular dysplasia initially diverted attention from primary hyperaldosteronism, delaying definitive diagnosis and curative treatment. Persistently suppressed renin and unexplained hypokalemia in the setting of uncontrolled hypertension, even after renal revascularization, should prompt clinicians to revisit the possibility of primary aldosteronism. This case underscores the importance of avoiding premature closure, maintaining vigilance for multiple etiologies, and reassessing the differential diagnosis when treatment of a plausible condition does not yield the expected clinical improvement.

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Publication Details

Journal
Cureus
Published
2025-11-05
DOI
https://doi.org/10.7759/cureus.96159
Primary Topic
Hormonal Regulation and Hypertension
Type
article
Field-Weighted Citation Impact
0.00

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article

Unmasking Secondary Hypertension: Renal Artery Stenosis Concealing the Diagnosis of Primary Hyperaldosteronism

Paul J. Wurtz, G. ICIE MACY, Alexandra Stewart, David L. Moore et al.
Cureus
Hormonal Regulation and Hypertension
article

Unmasking Secondary Hypertension: Renal Artery Stenosis Concealing the Diagnosis of Primary Hyperaldosteronism

Paul J. Wurtz, G. ICIE MACY, Alexandra Stewart, David L. Moore, Franchesca Farris Cosme
article en

Abstract

A 24-year-old woman with no prior comorbidities presented with severe, treatment-resistant hypertension characterized by episodic headaches and persistent systolic blood pressures above 140 mm Hg despite lifestyle modifications. Initial evaluation revealed hypokalemia and metabolic alkalosis with an aldosterone-to-renin ratio suggestive, but not diagnostic, of primary hyperaldosteronism. Secondary workup excluded pheochromocytoma, Cushing's syndrome, and thyroid disease. Imaging identified right renal artery fibromuscular dysplasia with angiographic narrowing of approximately 30%. Despite maximal medical therapy, her hypertension persisted, and repeat studies later demonstrated progression of stenosis to 70-75%, prompting angioplasty. The intervention improved arterial patency but failed to normalize her blood pressure or correct her tendency toward hypokalemia. Re-evaluation demonstrated a 1.7-cm left adrenal mass, and adrenal venous sampling confirmed unilateral aldosterone hypersecretion. The patient underwent laparoscopic adrenalectomy with pathology confirming an aldosterone-producing adenoma. Following surgery, she achieved normalization of potassium and sustained normotension without antihypertensive medications. This case highlights the diagnostic challenges when two secondary causes of hypertension coexist. Fibromuscular dysplasia initially diverted attention from primary hyperaldosteronism, delaying definitive diagnosis and curative treatment. Persistently suppressed renin and unexplained hypokalemia in the setting of uncontrolled hypertension, even after renal revascularization, should prompt clinicians to revisit the possibility of primary aldosteronism. This case underscores the importance of avoiding premature closure, maintaining vigilance for multiple etiologies, and reassessing the differential diagnosis when treatment of a plausible condition does not yield the expected clinical improvement.

CureusVol. 17(11)
Wilford Hall Ambulatory Surgical Center (US)
U.S. Department of Defense
Openalex Percentile: Top 56%
Hormonal Regulation and Hypertension
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