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Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan
Congenital renal anomalies are among the most common birth defects. They are often detected antenatally. If not, they can manifest in adulthood with variable clinical presentations. Herein, we present a case of a 72-year-old male patient who was incidentally found to have an extremely rare combinati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9471340/ https://www.ncbi.nlm.nih.gov/pubmed/36120523 http://dx.doi.org/10.1016/j.radcr.2022.08.039 |
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author | Saadeh, Ahmad Mahmoud, Muhannad M. Azizieh, Omar Al-Smair, Ali |
author_facet | Saadeh, Ahmad Mahmoud, Muhannad M. Azizieh, Omar Al-Smair, Ali |
author_sort | Saadeh, Ahmad |
collection | PubMed |
description | Congenital renal anomalies are among the most common birth defects. They are often detected antenatally. If not, they can manifest in adulthood with variable clinical presentations. Herein, we present a case of a 72-year-old male patient who was incidentally found to have an extremely rare combination of urinary tract defects comprising: right-sided unilateral renal agenesis, blind ureter, and ectopic ureterocele. |
format | Online Article Text |
id | pubmed-9471340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94713402022-09-15 Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan Saadeh, Ahmad Mahmoud, Muhannad M. Azizieh, Omar Al-Smair, Ali Radiol Case Rep Case Report Congenital renal anomalies are among the most common birth defects. They are often detected antenatally. If not, they can manifest in adulthood with variable clinical presentations. Herein, we present a case of a 72-year-old male patient who was incidentally found to have an extremely rare combination of urinary tract defects comprising: right-sided unilateral renal agenesis, blind ureter, and ectopic ureterocele. Elsevier 2022-09-09 /pmc/articles/PMC9471340/ /pubmed/36120523 http://dx.doi.org/10.1016/j.radcr.2022.08.039 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Saadeh, Ahmad Mahmoud, Muhannad M. Azizieh, Omar Al-Smair, Ali Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title | Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title_full | Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title_fullStr | Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title_full_unstemmed | Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title_short | Unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: An incidental finding on abdominal CT scan |
title_sort | unilateral renal agenesis, blind-ended ureter and ectopic ureterocele: an incidental finding on abdominal ct scan |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9471340/ https://www.ncbi.nlm.nih.gov/pubmed/36120523 http://dx.doi.org/10.1016/j.radcr.2022.08.039 |
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