Abstract

A renin-secreting renal tumor is a rare cause of curable hypertension characterized clinically by hypertension, hypokalemia, hyperaldosteronism and increased plasma renin activity (PRA). Prior subtotal adrenalectomy in such a patient allowed examination of the role of hyperreninemia in the absence of excessive aldosterone secretion. Hypertension was severe, but serum potassium and aldosterone production were normal. PRA was markedly increased under all conditions studied, with a persistent increase noted with changes in posture. Renal vein renin studies were critical in localizing the renal tumor, and unilateral nephrectomy resulted in a prompt fall in PRA to subnormal levels and dramatic cure of the hypertension. Renin content of the renal tumor was more than 500 times higher than in the adjacent kidney, and histologic studies confirmed that the tumor was of juxtaglomerular cell origin. This case demonstrates that severe hypertension can occur in this syndrome despite subtotal adrenalectomy and further illustrates an association of renin overproduction with a specific type of hypertension.

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