A pseudoaneurysm is an extraluminal collection of arterial blood, with turbulent flow, that results from blood flowing through a defect in an arterial wall. Uterine artery pseudoaneurysm (UAP) is a rare but life-threatening complication of uterine surgery such as Cesarean section 1 . It may be asymptomatic, may thrombose or may rupture, resulting in secondary postpartum hemorrhage (PPH) 1 -4 . The incidence of ruptured UAP has been estimated to be about 3% of all patients presenting with PPH 5 . Diagnosis of UAP generally involves color Doppler sonography and confirmation by angiography 1,2 . It can be treated with arterial embolization or hysterectomy, depending on clinical status 2 . We describe here our findings in a case of a giant UAP treated with a conservative approach. A 31-year-old woman delivered a 2750-g fetus by Cesarean section at 38 weeks' gestation. Uterine exteriorization, suturing and repositioning were sufficient to obtain adequate hemostasis. Before discharge from hospital, the woman underwent a pelvic ultrasound examination which revealed in the left lateral isthmic region a 49 × 39-mm hypoechoic cystic structure, consistent with a fluid collection. Color flow and spectral Doppler imaging revealed marked aliasing and bidirectional flow representing systolic and diastolic blood flow connected with the uterine artery of the ipsilateral side, which led to suspicion of pseudoaneurysm. Computed tomography was performed. Three-dimensional reconstruction of the resulting images revealed a large vascular neoformation,