# A Case of Ectopic Vas Deferens With Contralateral Vesicoureteral Reflux Causing Recurrent Pyelonephritis and Epididymitis

**Authors:** Kenichi Kobayashi, Kazuyoshi Johnin, Akinori Wada, Kazuaki Yamanaka, Susumu Kageyama

PMC · DOI: 10.7759/cureus.77209 · Cureus · 2025-01-09

## TL;DR

A four-year-old boy with a rare condition involving an ectopic vas deferens and urinary tract issues was successfully treated with surgery.

## Contribution

This case highlights the diagnostic challenges and management of ectopic vas deferens combined with vesicoureteral reflux.

## Key findings

- Ectopic vas deferens was connected to the bladder and caused recurrent infections.
- Surgical intervention resolved the infections and improved the patient's condition.

## Abstract

Ectopic vas deferens is a rare congenital anomaly and can be associated with urinary tract and genital anomalies. Therefore, patients can present with a variety of symptoms. We present the case of a four-year-old uncircumcised male patient with ectopic vas deferens and contralateral vesicoureteral reflux (VUR). Our patient had been caused breakthrough pyelonephritis and recurrent epididymitis alternately, and this made it difficult for us to reach an accurate diagnosis. The left vas deferens was connected to the bladder, and it was opening next to the left ureteral orifice. A bilateral ureteroneocystostomy and left vasectomy were performed, and the patient has been doing well and has had no further urinary tract infections (UTIs) or epididymitis.

## Linked entities

- **Diseases:** pyelonephritis (MONDO:0006939), epididymitis (MONDO:0004779), vesicoureteral reflux (MONDO:0006007)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** Pyelonephritis (MESH:D011704), urinary tract and genital anomalies (MESH:D014570), VUR (MESH:D014718), UTIs (MESH:D014552), Ectopic Vas Deferens (MESH:C535984), Epididymitis (MESH:D004823), congenital anomaly (MESH:D000013)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11807240/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC11807240/full.md

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Source: https://tomesphere.com/paper/PMC11807240