Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association.
Blind-ended ureter
Ectopic ureterocele
Renal agenesis
Journal
Urology case reports
ISSN: 2214-4420
Titre abrégé: Urol Case Rep
Pays: United States
ID NLM: 101626357
Informations de publication
Date de publication:
Sep 2023
Sep 2023
Historique:
received:
11
06
2023
revised:
09
07
2023
accepted:
13
07
2023
medline:
31
7
2023
pubmed:
31
7
2023
entrez:
31
7
2023
Statut:
epublish
Résumé
Congenital renal anomalies are common imaging findings and can often be detected antenatally. In some cases, these anomalies may go undetected and present in adulthood. We report a very rare case of unilateral renal agenesis in a 22-year-old male associated with an ipsilateral dilated blind-ended ureter that ectopically inserted into the seminal vesicle. This unique combination of developmental anomalies can lead to a variety of clinical presentations and requires careful monitoring and management.
Identifiants
pubmed: 37521279
doi: 10.1016/j.eucr.2023.102505
pii: S2214-4420(23)00191-2
pmc: PMC10371780
doi:
Types de publication
Case Reports
Langues
eng
Pagination
102505Informations de copyright
© 2023 The Authors.
Déclaration de conflit d'intérêts
There are no conflicts of interest.
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