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Retrocaval Ureter: Report of Two Cases
Retrocaval ureter (RCU) is a rare congenital anomaly in which the ureter passes posterior to the inferior vena cava (IVC). A little over 200 cases have been reported worldwide since Hochstetter's first report in 1893. We present two cases of retrocaval ureter which were successfully managed at...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875014/ https://www.ncbi.nlm.nih.gov/pubmed/31781468 http://dx.doi.org/10.1155/2019/2815748 |
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author | Atawurah, Henry Maison, Patrick Opoku Manu Owusu-Ansah, Mohammed Asante-Asamani, Alvin |
author_facet | Atawurah, Henry Maison, Patrick Opoku Manu Owusu-Ansah, Mohammed Asante-Asamani, Alvin |
author_sort | Atawurah, Henry |
collection | PubMed |
description | Retrocaval ureter (RCU) is a rare congenital anomaly in which the ureter passes posterior to the inferior vena cava (IVC). A little over 200 cases have been reported worldwide since Hochstetter's first report in 1893. We present two cases of retrocaval ureter which were successfully managed at the Cape Coast Teaching Hospital in Ghana. Case 1. A 55-year-old woman presented with a history of dull right flank pain of 2 years duration. Physical examination and basic laboratory investigations performed on her were normal. Abdominal ultrasound showed right hydronephrosis and a retrograde right ureteropyelogram (RPG) showed right hydroureteronephrosis with an “S” shaped proximal ureter. A diagnosis of retrocaval ureter was made and confirmed at surgery. Case 2. A 25-year-old man presented with dull intermittent right flank pain of 1 year duration. Clinical examination and laboratory investigation were normal. Abdominal ultrasound showed right hydronephrosis and a CT urogram made a diagnosis of retrocaval ureter which was confirmed at surgery. Conclusion. Retrocaval ureter is a rare congenital anomaly that is now increasingly being reported. Surgical treatment of symptomatic cases successfully relieves symptoms. |
format | Online Article Text |
id | pubmed-6875014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-68750142019-11-28 Retrocaval Ureter: Report of Two Cases Atawurah, Henry Maison, Patrick Opoku Manu Owusu-Ansah, Mohammed Asante-Asamani, Alvin Case Rep Urol Case Report Retrocaval ureter (RCU) is a rare congenital anomaly in which the ureter passes posterior to the inferior vena cava (IVC). A little over 200 cases have been reported worldwide since Hochstetter's first report in 1893. We present two cases of retrocaval ureter which were successfully managed at the Cape Coast Teaching Hospital in Ghana. Case 1. A 55-year-old woman presented with a history of dull right flank pain of 2 years duration. Physical examination and basic laboratory investigations performed on her were normal. Abdominal ultrasound showed right hydronephrosis and a retrograde right ureteropyelogram (RPG) showed right hydroureteronephrosis with an “S” shaped proximal ureter. A diagnosis of retrocaval ureter was made and confirmed at surgery. Case 2. A 25-year-old man presented with dull intermittent right flank pain of 1 year duration. Clinical examination and laboratory investigation were normal. Abdominal ultrasound showed right hydronephrosis and a CT urogram made a diagnosis of retrocaval ureter which was confirmed at surgery. Conclusion. Retrocaval ureter is a rare congenital anomaly that is now increasingly being reported. Surgical treatment of symptomatic cases successfully relieves symptoms. Hindawi 2019-11-03 /pmc/articles/PMC6875014/ /pubmed/31781468 http://dx.doi.org/10.1155/2019/2815748 Text en Copyright © 2019 Henry Atawurah et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Atawurah, Henry Maison, Patrick Opoku Manu Owusu-Ansah, Mohammed Asante-Asamani, Alvin Retrocaval Ureter: Report of Two Cases |
title | Retrocaval Ureter: Report of Two Cases |
title_full | Retrocaval Ureter: Report of Two Cases |
title_fullStr | Retrocaval Ureter: Report of Two Cases |
title_full_unstemmed | Retrocaval Ureter: Report of Two Cases |
title_short | Retrocaval Ureter: Report of Two Cases |
title_sort | retrocaval ureter: report of two cases |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875014/ https://www.ncbi.nlm.nih.gov/pubmed/31781468 http://dx.doi.org/10.1155/2019/2815748 |
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