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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-...

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Autores principales: Shangpliang, Darilin M, Rangad, Gordon, Das, Jayanta Kumar, Chakma, Kirtijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
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.
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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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