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Adult Wilms’ Tumour: Case Report and Review of Literature
Wilms’ tumour (nephroblastoma) is the most common renal tumour in children. Wilms’ tumour in adults is extremely rare and has a poorer prognosis than paediatric Wilms’ tumour. It is difficult to differentiate adult Wilms’ tumour from renal cell carcinoma based on radiological findings alone. The dia...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Codon Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347375/ https://www.ncbi.nlm.nih.gov/pubmed/28326278 http://dx.doi.org/10.15586/jkcvhl.2016.52 |
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author | Modi, Sunny Tiang, Kor Woi Inglis, Po Collins, Stuart |
author_facet | Modi, Sunny Tiang, Kor Woi Inglis, Po Collins, Stuart |
author_sort | Modi, Sunny |
collection | PubMed |
description | Wilms’ tumour (nephroblastoma) is the most common renal tumour in children. Wilms’ tumour in adults is extremely rare and has a poorer prognosis than paediatric Wilms’ tumour. It is difficult to differentiate adult Wilms’ tumour from renal cell carcinoma based on radiological findings alone. The diagnosis in adults is often serendipitous following nephrectomy for presumed renal cell carcinoma. Because of the paucity of literature, there are no standard protocols for the management of adult Wilms’ tumour, and therefore, it is managed as per paediatric Wilms’ tumour. Herein, we report the case of adult Wilms’ tumour in a 43-year-old man, which was diagnosed unexpectedly following nephrectomy for presumed renal cell carcinoma. |
format | Online Article Text |
id | pubmed-5347375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Codon Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-53473752017-03-21 Adult Wilms’ Tumour: Case Report and Review of Literature Modi, Sunny Tiang, Kor Woi Inglis, Po Collins, Stuart J Kidney Cancer VHL Case Report Wilms’ tumour (nephroblastoma) is the most common renal tumour in children. Wilms’ tumour in adults is extremely rare and has a poorer prognosis than paediatric Wilms’ tumour. It is difficult to differentiate adult Wilms’ tumour from renal cell carcinoma based on radiological findings alone. The diagnosis in adults is often serendipitous following nephrectomy for presumed renal cell carcinoma. Because of the paucity of literature, there are no standard protocols for the management of adult Wilms’ tumour, and therefore, it is managed as per paediatric Wilms’ tumour. Herein, we report the case of adult Wilms’ tumour in a 43-year-old man, which was diagnosed unexpectedly following nephrectomy for presumed renal cell carcinoma. Codon Publications 2016-05-23 /pmc/articles/PMC5347375/ /pubmed/28326278 http://dx.doi.org/10.15586/jkcvhl.2016.52 Text en Copyright © 2016 Codon Publications 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 |
spellingShingle | Case Report Modi, Sunny Tiang, Kor Woi Inglis, Po Collins, Stuart Adult Wilms’ Tumour: Case Report and Review of Literature |
title | Adult Wilms’ Tumour: Case Report and Review of Literature |
title_full | Adult Wilms’ Tumour: Case Report and Review of Literature |
title_fullStr | Adult Wilms’ Tumour: Case Report and Review of Literature |
title_full_unstemmed | Adult Wilms’ Tumour: Case Report and Review of Literature |
title_short | Adult Wilms’ Tumour: Case Report and Review of Literature |
title_sort | adult wilms’ tumour: case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347375/ https://www.ncbi.nlm.nih.gov/pubmed/28326278 http://dx.doi.org/10.15586/jkcvhl.2016.52 |
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