Bilateral complete ureter duplication presenting with hydronephrosis and spontaneous stone passage in a 25-year-old male: A rare case report.
Bilateral complete ureteral duplication
Case report
Hydronephrosis
Intravenous pyelograms
Ureteral stone
Ureteric duplication
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Oct 2024
Oct 2024
Historique:
received:
17
05
2024
revised:
12
07
2024
accepted:
13
07
2024
medline:
27
8
2024
pubmed:
27
8
2024
entrez:
27
8
2024
Statut:
epublish
Résumé
Ureteric duplication is a rare anomaly in the urinary tract, with an incidence of 0.5% to 3%. Bilateral double ureters are even rarer, occurring in 1 of 500 individuals. A 25-year-old man presented with right flank pain and nausea. Physical examination revealed tenderness at the right renal angle. Urinalysis demonstrated microscopic hematuria, and Ultrasound showed enlargement in the lower pole of the right kidney, while the upper pole appeared normal. Intravenous pyelography confirmed bilateral complete ureter duplication. However, after a week of observation, a 5 mm calcium oxalate stone was passed, and this event demonstrated the underlying cause of hydronephrosis in the lower pole of the right kidney. Bilateral complete ureter duplication is a rare anomaly in the urinary tract. To our knowledge, the presence of bilateral complete ureter duplication with a single stone in the right limb of the right double ureter is a unique case that has not been reported in the existing literature.
Identifiants
pubmed: 39188620
doi: 10.1016/j.radcr.2024.07.069
pii: S1930-0433(24)00656-3
pmc: PMC11345281
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
4482-4484Informations de copyright
© 2024 The Authors. Published by Elsevier Inc. on behalf of University of Washington.