Can Ureterocele Occur in a Non-Duplicated (Single) Collecting System?
Yes, ureteroceles absolutely can occur in kidneys with single, non-duplicated collecting systems, though they are less common than in duplex systems.
Epidemiology and Frequency
While ureteroceles are classically associated with duplicated collecting systems, single-system ureteroceles represent a well-documented entity. In one pediatric series, 9 children had ureteroceles with single collecting systems compared to 63 with duplex ureteroceles over an 8-year period—demonstrating that single-system ureteroceles comprise approximately 12-15% of all ureteroceles 1. Current guidelines recognize ureterocele as a cause of urinary tract dilation in both obstructive and non-obstructive contexts, without restricting the diagnosis to duplex systems 2.
Clinical Characteristics
Single-system ureteroceles differ from their duplex counterparts in several important ways:
- Gender distribution: Earlier reports suggested male predominance in single-system ectopic ureteroceles, but more recent data show equal gender distribution 1
- Associated anomalies: Single-system ureteroceles, particularly when associated with dysplastic kidneys, carry a significantly higher risk (63%) of other congenital anomalies including VACTERL association, congenital heart disease, and other genitourinary malformations 3
- Adult presentation: In adults, single-system ureteroceles are actually the predominant form, representing 94% of cases in one series, with duplex ureteroceles being rare 4
Clinical Presentations to Recognize
Single-system ureteroceles present with:
- Recurrent urinary tract infections (most common)
- Urinary retention or obstructive symptoms
- Hematuria
- Pelvic mass
- Urinary dribbling or incontinence (especially in females with ectopic insertion)
- Epididymitis in males
- Low back pain (adults)
- Associated stones (64% in adult series) 4
Diagnostic Approach
Key imaging findings that should raise suspicion:
- Ultrasound: Cystic dilation at the ureterovesical junction, hydroureteronephrosis
- VCUG: Characteristic "cobra head" or filling defect in bladder
- Critical pitfall: Nonvisualization of one kidney on imaging in association with any of the above symptoms should strongly suggest a single ectopic ureter with possible ureterocele 5
Management Considerations
Single-system ureteroceles require individualized assessment but generally follow this approach:
- High infection risk: Unlike some children with multicystic dysplastic kidney, this subgroup has increased infection risk and must be correctly identified for tailored management 3
- Conservative management: Careful evaluation with long-term surveillance is appropriate for many cases 1
- Spontaneous resolution: In cases with cystic/dysplastic kidneys, involution and reabsorption can occur with ureterocele collapse 1
- Endoscopic intervention: First-line for symptomatic cases without severe proximal dilation 4
- Watch for complications: De novo vesicoureteral reflux occurs in approximately 38.5% after endoscopic treatment 4
Common Pitfalls to Avoid
- Don't assume all ureteroceles are duplex: This outdated assumption delays diagnosis
- Screen for associated anomalies: Particularly in single-system cases with dysplastic kidneys
- Don't miss ectopic insertion: Pay particular attention to ureteral insertion site whenever reflux is present 5
- Consider prophylactic antibiotics: Children with known ureterocele are considered high-risk for UTI per current guidelines 2
The bottom line: Ureteroceles in single collecting systems are real, clinically significant, and require the same diagnostic vigilance as duplex-system ureteroceles, with particular attention to associated congenital anomalies.