Renal cell carcinoma in a duplex kidney in pediatric

Renal cell carcinoma (RCC) in children is relatively uncommon, especially in the absence of syndromes or hereditary diseases. Duplex kidney – as a common congenital anomalies in children – is usually insignificant with no serious impact or known risk of tumor association. Herein, we report a 5-year-...

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Autores principales: Alqarni, Naif, Alanazi, Awatif, Afaddagh, Abdulmohsin, Eldahshan, Samir, Alshayie, Mohammed, Alshammari, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343276/
https://www.ncbi.nlm.nih.gov/pubmed/34421274
http://dx.doi.org/10.4103/UA.UA_126_20
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author Alqarni, Naif
Alanazi, Awatif
Afaddagh, Abdulmohsin
Eldahshan, Samir
Alshayie, Mohammed
Alshammari, Ahmad
author_facet Alqarni, Naif
Alanazi, Awatif
Afaddagh, Abdulmohsin
Eldahshan, Samir
Alshayie, Mohammed
Alshammari, Ahmad
author_sort Alqarni, Naif
collection PubMed
description Renal cell carcinoma (RCC) in children is relatively uncommon, especially in the absence of syndromes or hereditary diseases. Duplex kidney – as a common congenital anomalies in children – is usually insignificant with no serious impact or known risk of tumor association. Herein, we report a 5-year-old girl who presented with gross hematuria and a right renal mass in duplex system identified on computed tomography. Radical nephrectomy was performed; the patient was diagnosed with Xp11 translocation RCC and no other modalities of treatments were needed over 3-month follow-up.
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spelling pubmed-83432762021-08-20 Renal cell carcinoma in a duplex kidney in pediatric Alqarni, Naif Alanazi, Awatif Afaddagh, Abdulmohsin Eldahshan, Samir Alshayie, Mohammed Alshammari, Ahmad Urol Ann Case Report Renal cell carcinoma (RCC) in children is relatively uncommon, especially in the absence of syndromes or hereditary diseases. Duplex kidney – as a common congenital anomalies in children – is usually insignificant with no serious impact or known risk of tumor association. Herein, we report a 5-year-old girl who presented with gross hematuria and a right renal mass in duplex system identified on computed tomography. Radical nephrectomy was performed; the patient was diagnosed with Xp11 translocation RCC and no other modalities of treatments were needed over 3-month follow-up. Wolters Kluwer - Medknow 2021 2021-07-14 /pmc/articles/PMC8343276/ /pubmed/34421274 http://dx.doi.org/10.4103/UA.UA_126_20 Text en Copyright: © 2021 Urology Annals https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Alqarni, Naif
Alanazi, Awatif
Afaddagh, Abdulmohsin
Eldahshan, Samir
Alshayie, Mohammed
Alshammari, Ahmad
Renal cell carcinoma in a duplex kidney in pediatric
title Renal cell carcinoma in a duplex kidney in pediatric
title_full Renal cell carcinoma in a duplex kidney in pediatric
title_fullStr Renal cell carcinoma in a duplex kidney in pediatric
title_full_unstemmed Renal cell carcinoma in a duplex kidney in pediatric
title_short Renal cell carcinoma in a duplex kidney in pediatric
title_sort renal cell carcinoma in a duplex kidney in pediatric
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343276/
https://www.ncbi.nlm.nih.gov/pubmed/34421274
http://dx.doi.org/10.4103/UA.UA_126_20
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AT alshayiemohammed renalcellcarcinomainaduplexkidneyinpediatric
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