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Bilateral ureteral triplication: A case report
Ureteral triplication is among the rarest congenital disorder of the urinary tract. A review of the literature has shown that only about one hundred cases have been reported worldwide. The reports on bilateral ureteral triplication cases, however, are extremely scarce. A female infant was presented...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574039/ https://www.ncbi.nlm.nih.gov/pubmed/33102104 http://dx.doi.org/10.1016/j.eucr.2020.101406 |
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author | Wahyudi, Irfan Fahri, Muhammad Situmorang, Gerhard Reinaldi Rodjani, Arry |
author_facet | Wahyudi, Irfan Fahri, Muhammad Situmorang, Gerhard Reinaldi Rodjani, Arry |
author_sort | Wahyudi, Irfan |
collection | PubMed |
description | Ureteral triplication is among the rarest congenital disorder of the urinary tract. A review of the literature has shown that only about one hundred cases have been reported worldwide. The reports on bilateral ureteral triplication cases, however, are extremely scarce. A female infant was presented with a history of recurrent febrile UTI since birth. Computed tomography urography scan revealed bilateral ureteral triplication. Combination of contrast studies and endoscopic procedure were utilized to establish the diagnosis. Management for this anomaly varies from conservative to interventional surgery. This patient underwent laparoscopic left ureteroneocystostomy and ureteral tailoring. |
format | Online Article Text |
id | pubmed-7574039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75740392020-10-23 Bilateral ureteral triplication: A case report Wahyudi, Irfan Fahri, Muhammad Situmorang, Gerhard Reinaldi Rodjani, Arry Urol Case Rep Pediatrics Ureteral triplication is among the rarest congenital disorder of the urinary tract. A review of the literature has shown that only about one hundred cases have been reported worldwide. The reports on bilateral ureteral triplication cases, however, are extremely scarce. A female infant was presented with a history of recurrent febrile UTI since birth. Computed tomography urography scan revealed bilateral ureteral triplication. Combination of contrast studies and endoscopic procedure were utilized to establish the diagnosis. Management for this anomaly varies from conservative to interventional surgery. This patient underwent laparoscopic left ureteroneocystostomy and ureteral tailoring. Elsevier 2020-09-10 /pmc/articles/PMC7574039/ /pubmed/33102104 http://dx.doi.org/10.1016/j.eucr.2020.101406 Text en © 2020 The Authors http://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 | Pediatrics Wahyudi, Irfan Fahri, Muhammad Situmorang, Gerhard Reinaldi Rodjani, Arry Bilateral ureteral triplication: A case report |
title | Bilateral ureteral triplication: A case report |
title_full | Bilateral ureteral triplication: A case report |
title_fullStr | Bilateral ureteral triplication: A case report |
title_full_unstemmed | Bilateral ureteral triplication: A case report |
title_short | Bilateral ureteral triplication: A case report |
title_sort | bilateral ureteral triplication: a case report |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574039/ https://www.ncbi.nlm.nih.gov/pubmed/33102104 http://dx.doi.org/10.1016/j.eucr.2020.101406 |
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