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Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature
Supernumerary kidney is a rare anomaly of number where commonly a third extra kidney exists with its own collecting system, blood supply, and encapsulated parenchyma. However, an extremely rare and unique diagnosis of bilateral supernumerary kidneys is also reported in few instances where two extra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880725/ https://www.ncbi.nlm.nih.gov/pubmed/35221730 http://dx.doi.org/10.2147/IMCRJ.S352605 |
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author | Tefera, Alemayehu Tegegne Gebreselassie, Kaleab Habtemichael Issack, Feysel Hassen Buser, Ashenafi Aberra Mummed, Ferid Ousman Dino, Masresha Solomon Gebrehiwot, Fitsum Gebreegziabher |
author_facet | Tefera, Alemayehu Tegegne Gebreselassie, Kaleab Habtemichael Issack, Feysel Hassen Buser, Ashenafi Aberra Mummed, Ferid Ousman Dino, Masresha Solomon Gebrehiwot, Fitsum Gebreegziabher |
author_sort | Tefera, Alemayehu Tegegne |
collection | PubMed |
description | Supernumerary kidney is a rare anomaly of number where commonly a third extra kidney exists with its own collecting system, blood supply, and encapsulated parenchyma. However, an extremely rare and unique diagnosis of bilateral supernumerary kidneys is also reported in few instances where two extra kidneys exist on each side of the body. Parenchymal fusion and the presence of good excretory function make the supernumerary kidneys even rarer as many of the reported cases are rudimentary organs. We present a 35-year-old man with a sudden onset of agonizing right flank pain and tenderness. Radiologic assessment with computed tomography showed bilaterally fussed and malrotated supernumerary kidneys with an obstructive stone and good contrast uptake. The patient has four fully functional kidneys (two on each side) with their own arterial supply, venous drainage, collecting system and incompletely duplicated ureters bilaterally. An open pyelolithotomy is performed to relieve pain and hydronephrosis. The patient’s symptoms improved after surgery and during subsequent follow-up. |
format | Online Article Text |
id | pubmed-8880725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-88807252022-02-26 Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature Tefera, Alemayehu Tegegne Gebreselassie, Kaleab Habtemichael Issack, Feysel Hassen Buser, Ashenafi Aberra Mummed, Ferid Ousman Dino, Masresha Solomon Gebrehiwot, Fitsum Gebreegziabher Int Med Case Rep J Case Report Supernumerary kidney is a rare anomaly of number where commonly a third extra kidney exists with its own collecting system, blood supply, and encapsulated parenchyma. However, an extremely rare and unique diagnosis of bilateral supernumerary kidneys is also reported in few instances where two extra kidneys exist on each side of the body. Parenchymal fusion and the presence of good excretory function make the supernumerary kidneys even rarer as many of the reported cases are rudimentary organs. We present a 35-year-old man with a sudden onset of agonizing right flank pain and tenderness. Radiologic assessment with computed tomography showed bilaterally fussed and malrotated supernumerary kidneys with an obstructive stone and good contrast uptake. The patient has four fully functional kidneys (two on each side) with their own arterial supply, venous drainage, collecting system and incompletely duplicated ureters bilaterally. An open pyelolithotomy is performed to relieve pain and hydronephrosis. The patient’s symptoms improved after surgery and during subsequent follow-up. Dove 2022-02-21 /pmc/articles/PMC8880725/ /pubmed/35221730 http://dx.doi.org/10.2147/IMCRJ.S352605 Text en © 2022 Tefera et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Tefera, Alemayehu Tegegne Gebreselassie, Kaleab Habtemichael Issack, Feysel Hassen Buser, Ashenafi Aberra Mummed, Ferid Ousman Dino, Masresha Solomon Gebrehiwot, Fitsum Gebreegziabher Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title | Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title_full | Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title_fullStr | Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title_full_unstemmed | Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title_short | Bilaterally Fused Supernumerary Kidneys: A Very Rare Case Report and Review of Literature |
title_sort | bilaterally fused supernumerary kidneys: a very rare case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880725/ https://www.ncbi.nlm.nih.gov/pubmed/35221730 http://dx.doi.org/10.2147/IMCRJ.S352605 |
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