SUMMARYA 24 year-old woman had a congenital solitary kidney with renovascular hypertension due to fibromuscular dysplasia. She had been treated as having essential hypertension until she developed preeclampsia and HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome at 28 weeks of gestation. Plasma renin activity and captopril test results did not indicate any abnormalities. However, renography revealed captoprilinduced deterioration. Magnetic resonance angiography was also useful to detect renal artery stenosis. These findings were confirmed by renal angiography. After successful percutaneous transluminal renal angioplasty, her blood pressure and the pattern of captopril renography normalized. (Int Heart J 2005; 46: 347-353) Key words: Captopril renography, Fibromuscular dysplasia, HELLP syndrome, Magnetic resonance angiography, Renovascular hypertension, Solitary kidney RENAL artery stenosis in a patient with a solitary kidney is relatively rare. As these patients are at a high risk of developing renal insufficiency, 1) accurate assessment of the renal blood supply is essential. While angiography provides the best imaging of renal arteries and remains the gold standard, it cannot evaluate renal function and is not completely risk-free. Captopril renography, which can be used to assess the response of each of the renal functions to the renin-angiotensin system, detects renovascular hypertension (RVHT) with high sensitivity and specificity. [2][3][4] This test is also considered useful for patients with a solitary kidney, although the extent to which hypertension and renal function depend on renin is still controversial. 5) We report here a patient with a congenital solitaryFrom the