In children with a duplex collecting system, also known as ureteral duplication, a kidney has two ureters (tubes that carry urine from the kidney to the bladder) rather than one.
Ureteral duplication is much more common in girls than in boys. No one knows the cause of ureteral duplication; some cases have been reported in siblings, suggesting a genetic component.
Often they are noticed before birth, when a prenatal ultrasound exam shows swelling (hydronephrosis) of a kidney. If a ureterocele isn't detected during pregnancy, it may not be detected until your child has recurrent urinary tract infections.
If your child has a history of frequent urinary tract infections, your child's physician may recommend the following tests:
Specific treatment recommendations for a ureterocele or ureteral duplication will depend on your child's individual situation.
If your child is ill from a urinary tract infection, intravenous fluids and antibiotics may be administered. Once the urinary tract infection is resolved, the ureterocele will be addressed.
If the area of the ureter has a great deal of urine accumulation, it may need to be surgically drained.
If your child's kidney has been damaged, part of it may need to be removed. For more information on that procedure, see our page on nephrectomy.
For more information, see our page on ureterocele.
A duplex collecting system and ureterocele are generally treated in tandem. Treatment of the ureterocele often depends on the size of the constriction and how well the kidney that the ureter drains is functioning.