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Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis

Congenital anomalies of the kidney and the urinary tract such as renal agenesis and ectopic ureter have complex development. These anomalies have variable presentations and associations. In this report, we highlight the case of a young man with congenital renal agenesis presenting for a urinary trac...

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Autores principales: El Hasbani, Georges, Assaker, Richard, Ahmad, Yasir J., Parashar, Kalind, Thomas, Ginu A., Maurer, Kyle, Gandhi, Darshan, Olsavsky, Thomas, Vargas, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753076/
https://www.ncbi.nlm.nih.gov/pubmed/33363676
http://dx.doi.org/10.1016/j.radcr.2020.12.022
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author El Hasbani, Georges
Assaker, Richard
Ahmad, Yasir J.
Parashar, Kalind
Thomas, Ginu A.
Maurer, Kyle
Gandhi, Darshan
Olsavsky, Thomas
Vargas, Jose
author_facet El Hasbani, Georges
Assaker, Richard
Ahmad, Yasir J.
Parashar, Kalind
Thomas, Ginu A.
Maurer, Kyle
Gandhi, Darshan
Olsavsky, Thomas
Vargas, Jose
author_sort El Hasbani, Georges
collection PubMed
description Congenital anomalies of the kidney and the urinary tract such as renal agenesis and ectopic ureter have complex development. These anomalies have variable presentations and associations. In this report, we highlight the case of a young man with congenital renal agenesis presenting for a urinary tract infection. Abdominal and pelvic computed tomography imaging revealed the rare association of renal agenesis with contralateral ectopic ureter and subsequent hydroureteronephrosis. A urinary tract infection can be the presenting complication of such association, and a long follow-up is needed to anticipate the management.
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spelling pubmed-77530762020-12-23 Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis El Hasbani, Georges Assaker, Richard Ahmad, Yasir J. Parashar, Kalind Thomas, Ginu A. Maurer, Kyle Gandhi, Darshan Olsavsky, Thomas Vargas, Jose Radiol Case Rep Case Report Congenital anomalies of the kidney and the urinary tract such as renal agenesis and ectopic ureter have complex development. These anomalies have variable presentations and associations. In this report, we highlight the case of a young man with congenital renal agenesis presenting for a urinary tract infection. Abdominal and pelvic computed tomography imaging revealed the rare association of renal agenesis with contralateral ectopic ureter and subsequent hydroureteronephrosis. A urinary tract infection can be the presenting complication of such association, and a long follow-up is needed to anticipate the management. Elsevier 2020-12-17 /pmc/articles/PMC7753076/ /pubmed/33363676 http://dx.doi.org/10.1016/j.radcr.2020.12.022 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. 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 Case Report
El Hasbani, Georges
Assaker, Richard
Ahmad, Yasir J.
Parashar, Kalind
Thomas, Ginu A.
Maurer, Kyle
Gandhi, Darshan
Olsavsky, Thomas
Vargas, Jose
Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title_full Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title_fullStr Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title_full_unstemmed Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title_short Renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
title_sort renal agenesis associated with contralateral ectopic ureter and hydroureteronephrosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753076/
https://www.ncbi.nlm.nih.gov/pubmed/33363676
http://dx.doi.org/10.1016/j.radcr.2020.12.022
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