Bilateral Botryoid Wilms Tumor presented with acute renal failure

Botryoid Wilms tumors are intrapelvic polypoid masses that are uncommon feature of Wilms tumor. The authors reported a rare case of bilateral botryoid Wilms tumor in a 19-month-old boy who admitted to hospital with acute renal failure secondary to hydronephrosis caused by bilateral botryoid Wilms tu...

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Detalles Bibliográficos
Autores principales: Bahoush, Gholamreza, Pahlavani, Rozhin, Salarinejad, Sareh, Zarei, Elham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677663/
https://www.ncbi.nlm.nih.gov/pubmed/33250947
http://dx.doi.org/10.1016/j.radcr.2020.10.055
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author Bahoush, Gholamreza
Pahlavani, Rozhin
Salarinejad, Sareh
Zarei, Elham
author_facet Bahoush, Gholamreza
Pahlavani, Rozhin
Salarinejad, Sareh
Zarei, Elham
author_sort Bahoush, Gholamreza
collection PubMed
description Botryoid Wilms tumors are intrapelvic polypoid masses that are uncommon feature of Wilms tumor. The authors reported a rare case of bilateral botryoid Wilms tumor in a 19-month-old boy who admitted to hospital with acute renal failure secondary to hydronephrosis caused by bilateral botryoid Wilms tumor with ureteral extension. The patient was successfully treated with chemotherapy and bilateral nephron sparing surgery in 2 separate operations. During 15 months follow-up, no evidence of recurrence or metastasis was found.
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spelling pubmed-76776632020-11-27 Bilateral Botryoid Wilms Tumor presented with acute renal failure Bahoush, Gholamreza Pahlavani, Rozhin Salarinejad, Sareh Zarei, Elham Radiol Case Rep Case Report Botryoid Wilms tumors are intrapelvic polypoid masses that are uncommon feature of Wilms tumor. The authors reported a rare case of bilateral botryoid Wilms tumor in a 19-month-old boy who admitted to hospital with acute renal failure secondary to hydronephrosis caused by bilateral botryoid Wilms tumor with ureteral extension. The patient was successfully treated with chemotherapy and bilateral nephron sparing surgery in 2 separate operations. During 15 months follow-up, no evidence of recurrence or metastasis was found. Elsevier 2020-11-13 /pmc/articles/PMC7677663/ /pubmed/33250947 http://dx.doi.org/10.1016/j.radcr.2020.10.055 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
Bahoush, Gholamreza
Pahlavani, Rozhin
Salarinejad, Sareh
Zarei, Elham
Bilateral Botryoid Wilms Tumor presented with acute renal failure
title Bilateral Botryoid Wilms Tumor presented with acute renal failure
title_full Bilateral Botryoid Wilms Tumor presented with acute renal failure
title_fullStr Bilateral Botryoid Wilms Tumor presented with acute renal failure
title_full_unstemmed Bilateral Botryoid Wilms Tumor presented with acute renal failure
title_short Bilateral Botryoid Wilms Tumor presented with acute renal failure
title_sort bilateral botryoid wilms tumor presented with acute renal failure
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677663/
https://www.ncbi.nlm.nih.gov/pubmed/33250947
http://dx.doi.org/10.1016/j.radcr.2020.10.055
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