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Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature

Wilms tumor, also denoted as nephroblastoma, an embryonal type of renal cancer, is the most common cancer that affects children in the first 5 years of life. Wilms tumor is very rarely seen in adults. Both adults and children showcase varied clinical symptoms. The metastasis of tumor in both adults...

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Detalles Bibliográficos
Autores principales: Sakthivel, Vishnupriya, Adeeb, Ismail Z, Vijayabalan, Devashree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Codon Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423726/
https://www.ncbi.nlm.nih.gov/pubmed/37583880
http://dx.doi.org/10.15586/jkcvhl.v10i3.281
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author Sakthivel, Vishnupriya
Adeeb, Ismail Z
Vijayabalan, Devashree
author_facet Sakthivel, Vishnupriya
Adeeb, Ismail Z
Vijayabalan, Devashree
author_sort Sakthivel, Vishnupriya
collection PubMed
description Wilms tumor, also denoted as nephroblastoma, an embryonal type of renal cancer, is the most common cancer that affects children in the first 5 years of life. Wilms tumor is very rarely seen in adults. Both adults and children showcase varied clinical symptoms. The metastasis of tumor in both adults and children are not uncommon. Though histological differences between children and adults are insignificant, the prognosis of adult Wilms tumors compared to children is abysmal. Despite remarkable advancements in oncology, no standard treatment protocol exists for Wilms tumor in adults. Children Wilms tumor treatment protocol is currently followed for adults with some changes. In this article, we reviewed the available treatment options for Wilms tumor in adults and protocols followed widely.
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spelling pubmed-104237262023-08-15 Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature Sakthivel, Vishnupriya Adeeb, Ismail Z Vijayabalan, Devashree J Kidney Cancer VHL Review Article Wilms tumor, also denoted as nephroblastoma, an embryonal type of renal cancer, is the most common cancer that affects children in the first 5 years of life. Wilms tumor is very rarely seen in adults. Both adults and children showcase varied clinical symptoms. The metastasis of tumor in both adults and children are not uncommon. Though histological differences between children and adults are insignificant, the prognosis of adult Wilms tumors compared to children is abysmal. Despite remarkable advancements in oncology, no standard treatment protocol exists for Wilms tumor in adults. Children Wilms tumor treatment protocol is currently followed for adults with some changes. In this article, we reviewed the available treatment options for Wilms tumor in adults and protocols followed widely. Codon Publications 2023-08-11 /pmc/articles/PMC10423726/ /pubmed/37583880 http://dx.doi.org/10.15586/jkcvhl.v10i3.281 Text en Copyright: Sakthivel V, et al. https://creativecommons.org/licenses/by/4.0/License: This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Review Article
Sakthivel, Vishnupriya
Adeeb, Ismail Z
Vijayabalan, Devashree
Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title_full Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title_fullStr Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title_full_unstemmed Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title_short Recent Improvements in Adult Wilms Tumor Diagnosis and Management: Review of Literature
title_sort recent improvements in adult wilms tumor diagnosis and management: review of literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423726/
https://www.ncbi.nlm.nih.gov/pubmed/37583880
http://dx.doi.org/10.15586/jkcvhl.v10i3.281
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