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Report of a rare testicular teratoid Wilms Tumor in an adult patient
Although primarily a pediatric disease, nephroblastomas (also known as Wilms tumor) occur in adults at a rate of less than 0.2 cases per million per year. Rarer still are teratoid Wilms tumors, which arise from teratomas and therefore can be extrarenal. We describe the sixth recorded case of a testi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529497/ https://www.ncbi.nlm.nih.gov/pubmed/34712587 http://dx.doi.org/10.1016/j.eucr.2021.101894 |
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author | Taros, T. Chabot, M. Sokoloff, M. Wollin, M. |
author_facet | Taros, T. Chabot, M. Sokoloff, M. Wollin, M. |
author_sort | Taros, T. |
collection | PubMed |
description | Although primarily a pediatric disease, nephroblastomas (also known as Wilms tumor) occur in adults at a rate of less than 0.2 cases per million per year. Rarer still are teratoid Wilms tumors, which arise from teratomas and therefore can be extrarenal. We describe the sixth recorded case of a testicular teratoid Wilms tumor in an adult patient with accompanying histological images of the specimen. Following the case, there is a brief discussion of the current literature. |
format | Online Article Text |
id | pubmed-8529497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85294972021-10-27 Report of a rare testicular teratoid Wilms Tumor in an adult patient Taros, T. Chabot, M. Sokoloff, M. Wollin, M. Urol Case Rep Oncology Although primarily a pediatric disease, nephroblastomas (also known as Wilms tumor) occur in adults at a rate of less than 0.2 cases per million per year. Rarer still are teratoid Wilms tumors, which arise from teratomas and therefore can be extrarenal. We describe the sixth recorded case of a testicular teratoid Wilms tumor in an adult patient with accompanying histological images of the specimen. Following the case, there is a brief discussion of the current literature. Elsevier 2021-10-12 /pmc/articles/PMC8529497/ /pubmed/34712587 http://dx.doi.org/10.1016/j.eucr.2021.101894 Text en © 2021 The Authors https://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 | Oncology Taros, T. Chabot, M. Sokoloff, M. Wollin, M. Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title | Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title_full | Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title_fullStr | Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title_full_unstemmed | Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title_short | Report of a rare testicular teratoid Wilms Tumor in an adult patient |
title_sort | report of a rare testicular teratoid wilms tumor in an adult patient |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529497/ https://www.ncbi.nlm.nih.gov/pubmed/34712587 http://dx.doi.org/10.1016/j.eucr.2021.101894 |
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