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Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases

Ewing sarcoma is an aggressive mesenchymal malignancy. It is the second most common bone tumor among children and adolescents and less commonly presents as a soft tissue or primary skin lesion. Cutaneous Ewing sarcoma has only been reported in case reports and case series. In this article, we descri...

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Autores principales: Tavakkoli, Montreh, Mueller, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276761/
https://www.ncbi.nlm.nih.gov/pubmed/30519175
http://dx.doi.org/10.1159/000492667
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author Tavakkoli, Montreh
Mueller, Lisa
author_facet Tavakkoli, Montreh
Mueller, Lisa
author_sort Tavakkoli, Montreh
collection PubMed
description Ewing sarcoma is an aggressive mesenchymal malignancy. It is the second most common bone tumor among children and adolescents and less commonly presents as a soft tissue or primary skin lesion. Cutaneous Ewing sarcoma has only been reported in case reports and case series. In this article, we describe a 12-year-old Hispanic female cured of localized, cutaneous Ewing sarcoma (pT1aN0M0) at the 40-month follow-up following surgical resection and adjuvant chemotherapy according to the COG AEWS1031 protocol for Ewing sarcoma of the bone. To our knowledge, this is the first article to provide a potential biological explanation for the differences in the prognosis of Ewing sarcoma of the bone, soft tissue, and skin.
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spelling pubmed-62767612018-12-05 Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases Tavakkoli, Montreh Mueller, Lisa Case Rep Oncol Case Report Ewing sarcoma is an aggressive mesenchymal malignancy. It is the second most common bone tumor among children and adolescents and less commonly presents as a soft tissue or primary skin lesion. Cutaneous Ewing sarcoma has only been reported in case reports and case series. In this article, we describe a 12-year-old Hispanic female cured of localized, cutaneous Ewing sarcoma (pT1aN0M0) at the 40-month follow-up following surgical resection and adjuvant chemotherapy according to the COG AEWS1031 protocol for Ewing sarcoma of the bone. To our knowledge, this is the first article to provide a potential biological explanation for the differences in the prognosis of Ewing sarcoma of the bone, soft tissue, and skin. S. Karger AG 2018-11-12 /pmc/articles/PMC6276761/ /pubmed/30519175 http://dx.doi.org/10.1159/000492667 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Tavakkoli, Montreh
Mueller, Lisa
Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title_full Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title_fullStr Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title_full_unstemmed Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title_short Cutaneous Ewing Sarcoma and Ewing Sarcoma of the Bone: Distinct Diseases
title_sort cutaneous ewing sarcoma and ewing sarcoma of the bone: distinct diseases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276761/
https://www.ncbi.nlm.nih.gov/pubmed/30519175
http://dx.doi.org/10.1159/000492667
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