Key result
Endoscopic adrenalectomy normalizes blood pressure and resolves primary aldosteronism at 4 months.
Why the study?
This case report aimed to demonstrate the clinical significance of timely detection of secondary hypertension in patients with resistant hypertension and severe cardiovascular complications.
Does timely diagnosis and endoscopic left adrenalectomy resolve resistant hypertension and severe hypokalemia in a patient with primary hyperaldosteronism due to an aldosterone-producing adenoma?
Case Report (n=1)
No
Does timely diagnosis and endoscopic left adrenalectomy resolve resistant hypertension and severe hypokalemia in a patient with primary hyperaldosteronism due to an aldosterone-producing adenoma?
This case report underscores that delayed screening for primary aldosteronism in patients with resistant hypertension and chronic hypokalemia can lead to recurrent disabling strokes, whereas timely diagnosis via the aldosterone-to-renin ratio and adrenalectomy achieves biochemical cure and blood pressure control.
Supports adrenalectomy for cure in this adenoma case; hypothesis-generating for stroke prevention via early primary aldosteronism screening.
Objective. The aim of the study is to demonstrate the clinical significance of the timely detection of secondary hypertension in patients with resistant hypertension and severe cardiovascular complications. Materials and Methods. We analyzed a clinical case of a 49-year-old female patient with long-standing resistant hypertension, multiple ischemic strokes, severe hypokalemia, and target organ damage. Clinical and laboratory evaluations were performed, including measurements of aldosterone and renin levels and the aldosterone-to-renin ratio (ARR). Adrenal imaging was conducted using computed tomography (CT). Results. The patient presented with persistent, poorly controlled hypertension despite multicomponent antihypertensive therapy, chronic severe hypokalemia. Notably, this hypokalemia had long been overlooked and had not prompted either a treatment revision or a targeted diagnostic workup. Additionally, hypernatremia, left ventricular hypertrophy, and sequelae of recurrent ischemic strokes were identified. Hormonal profiling revealed elevated aldosterone levels and an increased aldosterone-to-renin ratio. Computed tomography identified a left adrenal mass consistent with an aldosterone-producing adenoma. The patient underwent endoscopic left adrenalectomy. Postoperative outcomes included normalization of potassium levels, a decrease in aldosterone concentration, restoration of the aldosterone-to-renin ratio, and achievement of target blood pressure levels. It is highly probable that the prolonged, undiagnosed course of primary hyperaldosteronism was a major risk factor for the recurrent acute cerebrovascular events that resulted in the patient's permanent disability. Conclusion. This case highlights a prolonged, undiagnosed course of primary hyperaldosteronism associated with severe cerebrovascular complications and subsequent disability. In routine clinical practice, timely screening for primary hyperaldosteronism using the aldosterone-to-renin ratio in comorbid patients with resistant hypertension and hypokalemia could facilitate early diagnosis and ultimately improve patient outcomes.
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Goy et al. (2026) conducted a case report in Primary hyperaldosteronism (Conn's syndrome) with left aldosterone-producing adenoma, resistant hypertension, severe hypokalemia, and recurrent ischemic strokes (n=1). Endoscopic left adrenalectomy was evaluated on Postoperative blood pressure, serum potassium, aldosterone concentration, and aldosterone-to-renin ratio at 4 months.
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