Bilateral renal agenesis, a severe anomaly in a premature infant with VACTERL association: A case report
Journal Title: Pediatric Urology Case Reports - Year 2017, Vol 4, Issue 6
Abstract
We report on a preterm male (birth weight 1,100 g) with bilateral renal agenesis, a lethal malformation. Additionally, the child suffered from an atrial septal defect, ventricular septal defect, right aortic arch anomaly, a high type of anal atresia, vertebral anomalies, limbs defects (VACTERL association). The infant during first day of life was treated with an emergency sigmoid ostomy and peritoneal dialysis because of increasing abdominal dilatation and high urea and creatinine levels in blood. Important congenital anomalies associated with VACTERL association and prematurity are very serious causes of mortality in the early period.
Authors and Affiliations
Erol Basuguy, Sevinc Akdeniz, Sabahattin Ertugrul
Accessory urethra in a male infant: A case report
Accessory urethra is a rare congenital anomaly and has varied presentations. Multiple surgical techniques have been described for its correction. We report a case of accessory urethra in a male infant, which was recogniz...
Aphallia (Penile agenesis): A preliminary report of three cases
Aphallia (penile agenesis) is an extremely rare abnormality with the reported incidence of 1 in 30 million births. The cause of this anomaly is associated with no genital tubercle formation or its development impairment....
Acute bilateral ureteral obstruction following Dextranomer/hyaluronic acid polymer injection: A case report
Ureteral obstruction following bulking agent injection for treatment of vesicoureteral reflux is rare. Herein we report a case of acute bilateral ureteral obstruction following bilateral Dextranomer/hyaluronic acid polym...
Multiple stones in a pediatric case of single-system ureterocele with vesicoureteral reflux
Presence of multiple calculi in a single system ureterocele is a rare condition. A 3-year-old boy presented with recurrent urinary tract infections in whom multiple calculi were noted in the urinary bladder on x-ray and...
Monophasic Wilms’ tumor with multiple skeletal metastases in a young female: A case report and review of literature
Wilms’ tumor (nephroblastoma) is the most common renal tumor in children. It is uncommon in adolescent and skeletal metastasis at the time of presentation is even rare. The present case is a rare monophasic blastemal var...