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Renal lymphangiectasia in pediatric population: case series and review of literature
Renal lymphangiectasia is a rare disorder where perirenal, parapelvic, and/or intra-renal lymphatics are dilated. The clinical presentation of renal lymphangiectasia can range from asymptomatic to renal failure. Ultrasound, computed tomography and magnetic resonance imaging have been used for the di...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981996/ https://www.ncbi.nlm.nih.gov/pubmed/35380057 http://dx.doi.org/10.5144/0256-4947.2022.139 |
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author | Alshanafey, Saud Alkhani, Abdullah Alkibsib, Abdulaziz |
author_facet | Alshanafey, Saud Alkhani, Abdullah Alkibsib, Abdulaziz |
author_sort | Alshanafey, Saud |
collection | PubMed |
description | Renal lymphangiectasia is a rare disorder where perirenal, parapelvic, and/or intra-renal lymphatics are dilated. The clinical presentation of renal lymphangiectasia can range from asymptomatic to renal failure. Ultrasound, computed tomography and magnetic resonance imaging have been used for the diagnosis. Management of such cases varies from conservative to nephrectomy. We report three cases of pediatric renal lymphangiectasia that were managed by recurrent sclerothera-pies and medical supportive treatment at our institution. A literature review is also presented. To the best of our knowledge, there are 83 reported cases in the literature, 60 adults and 23 pediatrics. |
format | Online Article Text |
id | pubmed-8981996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | King Faisal Specialist Hospital and Research Centre |
record_format | MEDLINE/PubMed |
spelling | pubmed-89819962022-04-15 Renal lymphangiectasia in pediatric population: case series and review of literature Alshanafey, Saud Alkhani, Abdullah Alkibsib, Abdulaziz Ann Saudi Med Case Report Renal lymphangiectasia is a rare disorder where perirenal, parapelvic, and/or intra-renal lymphatics are dilated. The clinical presentation of renal lymphangiectasia can range from asymptomatic to renal failure. Ultrasound, computed tomography and magnetic resonance imaging have been used for the diagnosis. Management of such cases varies from conservative to nephrectomy. We report three cases of pediatric renal lymphangiectasia that were managed by recurrent sclerothera-pies and medical supportive treatment at our institution. A literature review is also presented. To the best of our knowledge, there are 83 reported cases in the literature, 60 adults and 23 pediatrics. King Faisal Specialist Hospital and Research Centre 2022-03 2022-04-07 /pmc/articles/PMC8981996/ /pubmed/35380057 http://dx.doi.org/10.5144/0256-4947.2022.139 Text en Copyright © 2022, Annals of Saudi Medicine, Saudi Arabia https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND). The details of which can be accessed at http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Case Report Alshanafey, Saud Alkhani, Abdullah Alkibsib, Abdulaziz Renal lymphangiectasia in pediatric population: case series and review of literature |
title | Renal lymphangiectasia in pediatric population: case series and review of literature |
title_full | Renal lymphangiectasia in pediatric population: case series and review of literature |
title_fullStr | Renal lymphangiectasia in pediatric population: case series and review of literature |
title_full_unstemmed | Renal lymphangiectasia in pediatric population: case series and review of literature |
title_short | Renal lymphangiectasia in pediatric population: case series and review of literature |
title_sort | renal lymphangiectasia in pediatric population: case series and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981996/ https://www.ncbi.nlm.nih.gov/pubmed/35380057 http://dx.doi.org/10.5144/0256-4947.2022.139 |
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