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The diagnostic journey in this case highlights the considerable challenges posed by congenital ureteral anomalies presenting in adulthood1,2, particularly when superimposed on pre-existing neurological conditions. In this patient, the presence of multiple sclerosis with established neurogenic bladder dysfunction created a diagnostic trap, leading to years of conservative management with intermittent catheterization and incontinence pads before the true anatomical anomaly was identified. This delay not only prolonged patient suffering but also permitted recurrent episodes of pyelonephritis and progressive upper tract deterioration, ultimately resulting in complete loss of upper pole function by the time of definitive diagnosis. The case underscores the critical importance of maintaining a high index of suspicion for congenital anomalies in adults with refractory incontinence, even when seemingly adequate explanations for symptoms exist.
The preoperative multimodal imaging strategy employed in this case proved essential for accurate anatomical delineation and surgical planning. Contrast-enhanced CT urography provided excellent visualization of the duplex system. The retrograde pyelography confirmed the ectopic insertion site, while MAG3 renal scintigraphy quantified the functional contribution of each moiety, confirming 0% differential function of the upper pole and establishing the lower pole's preserved function at 33% of total renal function. This comprehensive imaging approach is particularly valuable in complex cases where the anatomy may be distorted by chronic obstruction or recurrent infection, and it aligns with contemporary recommendations advocating for multimodality assessment prior to surgical intervention8,9.
The robotic surgical approach addressed several technical challenges inherent to this case, including the patient's significant comorbidities and the complex vascular anatomy of duplex kidneys. The patient's wheelchair dependence due to multiple sclerosis and bilateral hip arthroplasties necessitated careful positioning and secure fixation on the operating table, but did not preclude successful robotic intervention. The lateral decubitus positioning provided optimal access to both the renal fossa and the pelvic ureteral insertion, demonstrating the versatility of the robotic platform in managing anomalies spanning the entire retroperitoneal space7. ICG fluorescence guidance proved invaluable for precisely identifying the vascular supply to the lower pole moiety, allowing for selective clamping of the two small arteries supplying the upper pole while preserving perfusion to the functional renal tissue10,11. This technique, which has been increasingly adopted in robotic urologic surgery, enabled confident resection with minimal risk of ischemic injury to the preserved moiety6,7,12. The ability to verify perfusion both before and after resection using ICG provided real-time reassurance of lower pole viability and contributed to the zero-complication outcome.
The operative outcomes in this case compare favorably with published series of laparoscopic and robotic heminephrectomy in adults4,5. The operative time of 90 minutes, estimated blood loss of 50 mL, and absence of intraoperative complications reflect the benefits of robotic assistance. These technical advantages are particularly relevant in cases requiring meticulous dissection around the renal hilum and extensive ureteral mobilization down to the vaginal insertion. While previous reports have described laparoscopic approaches to similar pathology5, the robotic platform appears to offer advantages in terms of precision and surgeon comfort, especially when operating in confined spaces or when extensive ureteral dissection is required. The patient's hospital stay of four days was appropriate given her baseline functional limitations and the extent of the procedure, and the absence of postoperative complications suggests that the robotic approach is well-tolerated even in patients with significant neurological impairment.
The management of the ectopic ureter required particular attention to ensure complete resolution of incontinence without leaving a residual stump that could serve as a nidus for infection or continued leakage. The ureter was traced distally to its vaginal insertion and resected as low as possible, with the vaginal orifice closed using a surgical clip. The functional lower pole ureter was preserved intact to the ureterovesical junction, as confirmed by ICG fluorescence demonstrating adequate perfusion along its entire course. The 12-month follow-up confirms the durability of this approach, and the stable renal function (33% split function on the right) indicates that the preserved lower pole is providing adequate drainage without obstruction or reflux.
In this 41-year-old patient with multiple sclerosis and a duplex kidney with a non-functioning upper pole moiety and vaginal ectopic megaureter, robotic-assisted heminephroureterectomy with ICG fluorescence guidance resulted in complete resolution of incontinence and recurrent infections, with preserved lower-pole renal function at 12 months. While these results are encouraging for this individual patient, they should not be interpreted as establishing the general safety and efficacy of robotic heminephroureterectomy across all patient populations, as outcomes depend heavily on patient-specific anatomy, surgeon expertise, and institutional resources. Further studies in larger, more diverse cohorts are necessary to define the role of this approach in the broader management of complex congenital urogenital anomalies in adults.