We report the case of a 22-year-old female patient who attended the department of nephrology for arterial hypertension. She had no remarkable personal or family history. Physical examination revealed a sitting blood
pressure of 175/100 mmHg and a heart rate of 76 beats per minute. Examination was otherwise unremarkable. Supplemental tests, including complete blood count, biochemistry, urinary catecholamines, urine sediment, chest Xrays, and electrocardiogram, were normal. Treatment was started with bisoprolol, and an angio-MRI was requested for renal study. At 3 months of treatment, the patient showed a slight improvement in her blood pressure values (160/90 mmHg), and angio-MRI revealed doubtful fibrodysplasia at left renal artery level. Renal arteriography was therefore performed for confirmation. Arteriography showed critical stenosis in the right renal segmental artery with collateral circulation and no significant lesions in left renal artery. Angioplasty was performed on this stenosis using a 4 x 20 mm balloon catheter with good morphological result and disappearance of collateral circulation (fig. 1). At 2 years of follow-up, the patient has normal blood pressure values under no drug treatment.
Fibromuscular dysplasia usually occurs in young women aged 15-50 years, and the arterial sector usually affected are the distal 2/3 of the renal artery. RVH caused by involvement of renal artery branches is rare, and in the reported cases the polar arteries3 or the accessory arteries4 were affected. In our case, RVH was caused by involvement of a main branch of the right renal artery. RVH resulting from involvement of this segmental artery is an exceptional case. As regards treatment, advances in endovascular procedures in recent years have allowed for a high success rate in therapeutic management of these patients.