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Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report

Myxoid variant of chondrosarcoma is an uncommon potentially lethal malignant tumor which is even rare in pediatric age group. In the present paper, we report one such case of intermediate grade myxoid chondrosarcoma of left side of maxilla in a 12-year-old girl. The present case had a firm, painless...

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Autores principales: Nimonkar, Pranali, Bhola, Nitin, Jadhav, Anendd, Jain, Anuj, Borle, Rajiv, Ranka, Rajul, Chaudhary, Minal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745617/
https://www.ncbi.nlm.nih.gov/pubmed/26904332
http://dx.doi.org/10.1155/2016/5419737
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author Nimonkar, Pranali
Bhola, Nitin
Jadhav, Anendd
Jain, Anuj
Borle, Rajiv
Ranka, Rajul
Chaudhary, Minal
author_facet Nimonkar, Pranali
Bhola, Nitin
Jadhav, Anendd
Jain, Anuj
Borle, Rajiv
Ranka, Rajul
Chaudhary, Minal
author_sort Nimonkar, Pranali
collection PubMed
description Myxoid variant of chondrosarcoma is an uncommon potentially lethal malignant tumor which is even rare in pediatric age group. In the present paper, we report one such case of intermediate grade myxoid chondrosarcoma of left side of maxilla in a 12-year-old girl. The present case had a firm, painless, and lobulated growth in premolar-molar region which was associated with bicortical expansion. Maxillofacial imaging showed ill-defined radiolucency with displaced maxillary molars. Osteolytic changes were evident with the alveolus and walls of maxillary sinus. Owing to the age of the patient, surgical excision was selected as the modality of management followed by postoperative radiotherapy. This report encompasses the entire gamut of clinicopathological, radiological, and treatment modalities employed for chondrosarcoma.
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spelling pubmed-47456172016-02-22 Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report Nimonkar, Pranali Bhola, Nitin Jadhav, Anendd Jain, Anuj Borle, Rajiv Ranka, Rajul Chaudhary, Minal Case Rep Oncol Med Case Report Myxoid variant of chondrosarcoma is an uncommon potentially lethal malignant tumor which is even rare in pediatric age group. In the present paper, we report one such case of intermediate grade myxoid chondrosarcoma of left side of maxilla in a 12-year-old girl. The present case had a firm, painless, and lobulated growth in premolar-molar region which was associated with bicortical expansion. Maxillofacial imaging showed ill-defined radiolucency with displaced maxillary molars. Osteolytic changes were evident with the alveolus and walls of maxillary sinus. Owing to the age of the patient, surgical excision was selected as the modality of management followed by postoperative radiotherapy. This report encompasses the entire gamut of clinicopathological, radiological, and treatment modalities employed for chondrosarcoma. Hindawi Publishing Corporation 2016 2016-01-24 /pmc/articles/PMC4745617/ /pubmed/26904332 http://dx.doi.org/10.1155/2016/5419737 Text en Copyright © 2016 Pranali Nimonkar et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nimonkar, Pranali
Bhola, Nitin
Jadhav, Anendd
Jain, Anuj
Borle, Rajiv
Ranka, Rajul
Chaudhary, Minal
Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title_full Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title_fullStr Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title_full_unstemmed Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title_short Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report
title_sort myxoid chondrosarcoma of maxilla in a pediatric patient: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745617/
https://www.ncbi.nlm.nih.gov/pubmed/26904332
http://dx.doi.org/10.1155/2016/5419737
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