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Primary Adult Renal Ewing’s Sarcoma: A Rare Entity
Ewing’s sarcoma/primitive neuroectodermal tumors are high-grade small round blue cell tumors traditionally found in children and adolescents.These tumors primarily affect the bone and soft tissue, with extraskeletal sites rarely being affected. The clinical presentation and imaging findings are non-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933607/ https://www.ncbi.nlm.nih.gov/pubmed/35350532 http://dx.doi.org/10.7759/cureus.22302 |
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author | Shangpliang, Darilin M Rangad, Gordon Das, Jayanta Kumar Chakma, Kirtijit |
author_facet | Shangpliang, Darilin M Rangad, Gordon Das, Jayanta Kumar Chakma, Kirtijit |
author_sort | Shangpliang, Darilin M |
collection | PubMed |
description | Ewing’s sarcoma/primitive neuroectodermal tumors are high-grade small round blue cell tumors traditionally found in children and adolescents.These tumors primarily affect the bone and soft tissue, with extraskeletal sites rarely being affected. The clinical presentation and imaging findings are non-specific and are not characteristic. The diagnosis is essentially based on the histopathologic findings assisted by immunohistochemistry and/or cytogenetic molecular studies. Proper diagnoses and timely management of this tumor are essential owing to the aggressive nature and poor prognosis of the disease. |
format | Online Article Text |
id | pubmed-8933607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-89336072022-03-28 Primary Adult Renal Ewing’s Sarcoma: A Rare Entity Shangpliang, Darilin M Rangad, Gordon Das, Jayanta Kumar Chakma, Kirtijit Cureus Pathology Ewing’s sarcoma/primitive neuroectodermal tumors are high-grade small round blue cell tumors traditionally found in children and adolescents.These tumors primarily affect the bone and soft tissue, with extraskeletal sites rarely being affected. The clinical presentation and imaging findings are non-specific and are not characteristic. The diagnosis is essentially based on the histopathologic findings assisted by immunohistochemistry and/or cytogenetic molecular studies. Proper diagnoses and timely management of this tumor are essential owing to the aggressive nature and poor prognosis of the disease. Cureus 2022-02-16 /pmc/articles/PMC8933607/ /pubmed/35350532 http://dx.doi.org/10.7759/cureus.22302 Text en Copyright © 2022, Shangpliang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Pathology Shangpliang, Darilin M Rangad, Gordon Das, Jayanta Kumar Chakma, Kirtijit Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title | Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title_full | Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title_fullStr | Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title_full_unstemmed | Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title_short | Primary Adult Renal Ewing’s Sarcoma: A Rare Entity |
title_sort | primary adult renal ewing’s sarcoma: a rare entity |
topic | Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933607/ https://www.ncbi.nlm.nih.gov/pubmed/35350532 http://dx.doi.org/10.7759/cureus.22302 |
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