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Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case

Clear cell sarcoma of soft tissue is a rare, aggressive soft tissue tumor, which is morphologically similar to malignant melanoma but has no precursor skin lesion and, instead, has a characteristic chromosomal translocation. It is critical, yet challenging, to recognize clear cell sarcoma of soft ti...

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Detalles Bibliográficos
Autores principales: Leng, Bing, Zhang, Xinmin, Ali, Sayed, Karpo, Marc, Singh, Salil, Herpen, Robert, Zhang, Paul J., Khurana, Jasvir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433018/
https://www.ncbi.nlm.nih.gov/pubmed/22949909
http://dx.doi.org/10.1159/000342068
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author Leng, Bing
Zhang, Xinmin
Ali, Sayed
Karpo, Marc
Singh, Salil
Herpen, Robert
Zhang, Paul J.
Khurana, Jasvir S.
author_facet Leng, Bing
Zhang, Xinmin
Ali, Sayed
Karpo, Marc
Singh, Salil
Herpen, Robert
Zhang, Paul J.
Khurana, Jasvir S.
author_sort Leng, Bing
collection PubMed
description Clear cell sarcoma of soft tissue is a rare, aggressive soft tissue tumor, which is morphologically similar to malignant melanoma but has no precursor skin lesion and, instead, has a characteristic chromosomal translocation. It is critical, yet challenging, to recognize clear cell sarcoma of soft tissue because the outcome is very different to that of metastatic melanoma. We report a case of clear cell sarcoma of soft tissue arising in the left foot of a 35-year-old African-American woman.
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spelling pubmed-34330182012-09-04 Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case Leng, Bing Zhang, Xinmin Ali, Sayed Karpo, Marc Singh, Salil Herpen, Robert Zhang, Paul J. Khurana, Jasvir S. Case Rep Oncol Published online: August, 2012 Clear cell sarcoma of soft tissue is a rare, aggressive soft tissue tumor, which is morphologically similar to malignant melanoma but has no precursor skin lesion and, instead, has a characteristic chromosomal translocation. It is critical, yet challenging, to recognize clear cell sarcoma of soft tissue because the outcome is very different to that of metastatic melanoma. We report a case of clear cell sarcoma of soft tissue arising in the left foot of a 35-year-old African-American woman. S. Karger AG 2012-08-22 /pmc/articles/PMC3433018/ /pubmed/22949909 http://dx.doi.org/10.1159/000342068 Text en Copyright © 2012 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No-Derivative-Works License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: August, 2012
Leng, Bing
Zhang, Xinmin
Ali, Sayed
Karpo, Marc
Singh, Salil
Herpen, Robert
Zhang, Paul J.
Khurana, Jasvir S.
Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title_full Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title_fullStr Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title_full_unstemmed Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title_short Clear Cell Sarcoma: A Case Report with Radiological and Pathological Features of an Atypical Case
title_sort clear cell sarcoma: a case report with radiological and pathological features of an atypical case
topic Published online: August, 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433018/
https://www.ncbi.nlm.nih.gov/pubmed/22949909
http://dx.doi.org/10.1159/000342068
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