Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association

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 ur...

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Detalles Bibliográficos
Autores principales: Sorour, Sara, Ferguson, Craig, Wilson, Mitchell P., Low, Gavin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Functional Urology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371780/
https://www.ncbi.nlm.nih.gov/pubmed/37521279
http://dx.doi.org/10.1016/j.eucr.2023.102505
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author Sorour, Sara
Ferguson, Craig
Wilson, Mitchell P.
Low, Gavin
author_facet Sorour, Sara
Ferguson, Craig
Wilson, Mitchell P.
Low, Gavin
author_sort Sorour, Sara
collection PubMed
description 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.
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spelling pubmed-103717802023-07-28 Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association Sorour, Sara Ferguson, Craig Wilson, Mitchell P. Low, Gavin Urol Case Rep Functional Urology 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. Elsevier 2023-07-13 /pmc/articles/PMC10371780/ /pubmed/37521279 http://dx.doi.org/10.1016/j.eucr.2023.102505 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Functional Urology
Sorour, Sara
Ferguson, Craig
Wilson, Mitchell P.
Low, Gavin
Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title_full Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title_fullStr Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title_full_unstemmed Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title_short Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association
title_sort unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: a very rare developmental association
topic Functional Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371780/
https://www.ncbi.nlm.nih.gov/pubmed/37521279
http://dx.doi.org/10.1016/j.eucr.2023.102505
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