Introduction: Ureteral atresia is a rare disease usually associated with a non-functioning kidney. Its association with other urinary anomalies is rare. Case presentation: In this study we discuss the possibility of congenital or acquired etiology of a right imperforate distal ureter. Here we report the case of 11-month-old white boy with a right ureteropelvic junction obstruction. He underwent a right pyeloplasty when he was 11-months old, and 3 weeks after surgery a cystoscopy was performed. Two months after the first operation, he underwent a right ureteral meatoplasty and a new pyeloplasty. Conclusions: To the best of our knowledge, few cases of imperforate distal ureter have been described in the literature. The suspicion of a non-patent terminal ureter, occurring during upper urinary tract surgery, must be intraoperatively clarified to preserve the renal function and to avoid more complex surgical approaches.
|Titolo:||Hypothesis of an acquired etiopathogenesis of imperforate distal ureter: a case report|
|Data di pubblicazione:||2015|
|Citazione:||Hypothesis of an acquired etiopathogenesis of imperforate distal ureter: a case report / V Bagnara; Castorina S; S Gerocarni Nappo; G Privitera; T Luca; P Caione. - In: JOURNAL OF MEDICAL CASE REPORTS. - ISSN 1752-1947. - 9(2015), p. 227.|
|Appare nelle tipologie:||1.1 Articolo in rivista|