A Rare Case Report Of Incidentally Picked Up Ipsilateral Renal Agenesis, Blind Ending Proximal Megaureter And Ureterocele In An Adult

Authors

  • Astha Agrawal
  • Ashwin Kumar. A
  • Nisarga B V
  • G. Murugan

DOI:

https://doi.org/10.63682/jns.v14i14S.4349

Keywords:

Renal agenesis, Blind ending ureter, Megaureter, Ureterocele

Abstract

Congenital renal anomalies are the most common birth defects. They are detected antenatally. If not, they can manifest in adulthood with variable presentation. Here we present a case of 30-year-old male patient who presented with left lumbar pain and recurrent UTI. On Radiological evaluation he was found to have unilateral left renal agenesis with ipsilateral cranial blind ending megaureter and ureterocele

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References

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Sorour, S., Ferguson, C., Wilson, M. & Low, G., 2013. Sorour S, Ferguson C, Wilson MP, Low G (2023 Jul 13). 'Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association'. .50:102505.. Urol Case Report, Volume 50, p. 102505.

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Published

2025-04-22

How to Cite

1.
Agrawal A, Kumar. A A, B V N, G. Murugan GM. A Rare Case Report Of Incidentally Picked Up Ipsilateral Renal Agenesis, Blind Ending Proximal Megaureter And Ureterocele In An Adult. J Neonatal Surg [Internet]. 2025Apr.22 [cited 2025Sep.19];14(14S):866-9. Available from: https://www.jneonatalsurg.com/index.php/jns/article/view/4349