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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...

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Detalles Bibliográficos
Autores principales: Wahyudi, Irfan, Fahri, Muhammad, Situmorang, Gerhard Reinaldi, Rodjani, Arry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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