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Ewing's sarcoma of maxilla: A rare case report

Ewing's sarcoma is uncommon malignancy of childhood, frequently involving the mandible. The occurrence in maxilla is rare. It is histopathologically characterized by sheets of round cells positive for CD99. Although the prognosis is poor but early diagnosis and long term follow up can improve t...

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Autores principales: Jairamdas Nagpal, Deepak Kumar, Prabhu, Prashant Ramesh, Palaskar, Sangeeta Jayant, Patil, Swati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196295/
https://www.ncbi.nlm.nih.gov/pubmed/25328307
http://dx.doi.org/10.4103/0973-029X.140769
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author Jairamdas Nagpal, Deepak Kumar
Prabhu, Prashant Ramesh
Palaskar, Sangeeta Jayant
Patil, Swati
author_facet Jairamdas Nagpal, Deepak Kumar
Prabhu, Prashant Ramesh
Palaskar, Sangeeta Jayant
Patil, Swati
author_sort Jairamdas Nagpal, Deepak Kumar
collection PubMed
description Ewing's sarcoma is uncommon malignancy of childhood, frequently involving the mandible. The occurrence in maxilla is rare. It is histopathologically characterized by sheets of round cells positive for CD99. Although the prognosis is poor but early diagnosis and long term follow up can improve the survival. This article presents a rare case of Ewing's sarcoma of maxilla in a 15 year old male patient showing excessive fibro-osseous response which is not a frequent presentation. A retrospective analysis of cases of Ewings sarcoma of maxilla published in the English litreture is reviewed. In our case, diagnosis was confirmed by immunohistochemistry where sheets of round tumor cells were positive for CD 99. Ewings sarcoma of maxilla is a rare and aggressive tumor. Hence early diagnosis, combined therapy and long term follow up is suggested in such cases.
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spelling pubmed-41962952014-10-17 Ewing's sarcoma of maxilla: A rare case report Jairamdas Nagpal, Deepak Kumar Prabhu, Prashant Ramesh Palaskar, Sangeeta Jayant Patil, Swati J Oral Maxillofac Pathol Case Report Ewing's sarcoma is uncommon malignancy of childhood, frequently involving the mandible. The occurrence in maxilla is rare. It is histopathologically characterized by sheets of round cells positive for CD99. Although the prognosis is poor but early diagnosis and long term follow up can improve the survival. This article presents a rare case of Ewing's sarcoma of maxilla in a 15 year old male patient showing excessive fibro-osseous response which is not a frequent presentation. A retrospective analysis of cases of Ewings sarcoma of maxilla published in the English litreture is reviewed. In our case, diagnosis was confirmed by immunohistochemistry where sheets of round tumor cells were positive for CD 99. Ewings sarcoma of maxilla is a rare and aggressive tumor. Hence early diagnosis, combined therapy and long term follow up is suggested in such cases. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4196295/ /pubmed/25328307 http://dx.doi.org/10.4103/0973-029X.140769 Text en Copyright: © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jairamdas Nagpal, Deepak Kumar
Prabhu, Prashant Ramesh
Palaskar, Sangeeta Jayant
Patil, Swati
Ewing's sarcoma of maxilla: A rare case report
title Ewing's sarcoma of maxilla: A rare case report
title_full Ewing's sarcoma of maxilla: A rare case report
title_fullStr Ewing's sarcoma of maxilla: A rare case report
title_full_unstemmed Ewing's sarcoma of maxilla: A rare case report
title_short Ewing's sarcoma of maxilla: A rare case report
title_sort ewing's sarcoma of maxilla: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196295/
https://www.ncbi.nlm.nih.gov/pubmed/25328307
http://dx.doi.org/10.4103/0973-029X.140769
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