Ureterocele | Ureterocele Incision | Ureterocele Disproportion скачать в хорошем качестве

Ureterocele | Ureterocele Incision | Ureterocele Disproportion

A complete duplicated system ureterocele refers to a congenital abnormality where a ureterocele (a cystic dilation of the distal ureter) is associated with the upper pole moiety of a completely duplicated renal collecting system. This condition is typically seen in pediatric patients and is more common in females. Surgical Management: Depends on symptom severity and renal function: Endoscopic Puncture: Minimally invasive decompression of the ureterocele. First-line for neonates with obstruction. Upper Pole Nephrectomy: If the upper pole is non-functional. Ureteral Reimplantation: Corrects associated reflux or improves drainage. Hemi-Nephroureterectomy: Removes the non-functioning upper pole and its ureter. Prognosis: With timely diagnosis and appropriate intervention, outcomes are generally favorable, preserving renal function and reducing long-term complications. Regular follow-up with imaging and renal function assessment is essential.