A 54-year-old woman with a history of cesarean section five months ago was evaluated for one episode of gross hematuria in an outpatient setting. She had no other symptoms. Her vital signs were stable and her hemoglobin was 12.1 g/dL. Urinary tract ultrasonography showed a lobulated cystic mass at the lower pole of left kidney. Intravenous pyelogram showed duplicated collecting system and lower pyelocalyceal dilatation of the left kidney. Abdominopelvic CT angiography demonstrated an enhanced space-occupying mass on the left pyelocalyceal system suggestive of malignant tumor. Given these data right nephrectomy was recommended to the patient but she refused nephrectomy and further evaluation. After nine years she was admitted to the hospital because of a severe left flank pain and an abdominal pain. She had no hematuria and other urinary tract symptoms in the last admission. On review of system she had shortness of breath (NYHA functional class II) and infrequent headaches. On examination, the blood pressure was 150/90 mmHg, the pulse was 110 beats per minute; the temperature was 37.2°C and the respiratory rate 20 breaths per minutes. Cardiac auscultation revealed a crescendo-decrescendo systolic murmur at the right upper sternal border and an S3. A continuous bruit with systolic accentuation was audible over the abdomen particularly left upper quadrant. The rest of the general examinations were normal. Her laboratory data were within normal limit. An electrocardiogram revealed tachycardia and left ventricular hypertrophy. A chest radiograph was normal. Transthoracic echocardiography showed decreased left ventricular ejection fraction (LVEF = 40%), mild left ventricular dilatation (left ventricular end diastolic diameter = 5.7 cm), mild left ventricular hypertrophy (interventricular septal thickness = 1.2 cm and posterior wall thickness = 1.1 cm) and increased left ventricular mass index (LVMI = 162.9 g/m
2). According to her past medical history, abdominopelvic CT angiography was performed and it showed early filling of left renal vein, almost at the same time of left renal artery filling most probably due to arteriovenous fistula (
Figure 1). To definite the diagnosis and possible interventional management, renal arteries angiography was performed and it demonstrated a large left renal arteriovenous fistula with early opacification of the dilated renal vein and weak left renal parenchymal opacification (
Figure 2A). According to acceptable anatomy for endovascular treatment, and patient’s symptoms and signs, coil-embolization of arteriovenous fistula was done (with a 14 diameter Nit-occlude VSD coil). The post embolization angiogram revealed a direct flow via the renal artery to the parenchyma and then normal filling of the renal vein. There was no blood flow via the previous fistula. The procedure did not have any complications such as a partial renal infarction (
Figure 2B). The patient was discharged on the second post procedural day with good conditions. After 6 months of follow-up, the patient had complete disappearance of gross hematuria episodes, flank pain, headache and dyspnea. Her blood pressure and heart rate decreased (blood pressure 135/80 mmHg and heart rate 80 beats per minute). On duplex ultrasonography there was no flow via the previous fistula. Color doppler and hemodynamic study of the renal vein were normal. Transthoracic echocardiography was performed for the second time and it showed normalization of the past data (left ventricular ejection fraction; 50%, left ventricular end diastolic diameter of 5.3 cm, interventricular septal thickness of 1 cm, posterior wall thickness=0.9cm and left ventricular mass index about 109.6 g/m
2).