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Ewing's Sarcoma of Mandible: A Case Report with Review
AIM: To make dentists and pedodontists aware of a possible outcome of a rapidly growing swelling. BACKGROUND: Ewing's sarcoma is a rare aggressive variant of small round cell tumors and is an uncommon malignancy that occurs usually in childhood. It constitutes 10–15% of all primary malignant tu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Jaypee Brothers Medical Publishers
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229355/ https://www.ncbi.nlm.nih.gov/pubmed/32440057 http://dx.doi.org/10.5005/jp-journals-10005-1665 |
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author | Ahuja, Upasana S Puri, Nidhi Gupta, Deepak Singh, Shivangi Kumar, Gyanendra |
author_facet | Ahuja, Upasana S Puri, Nidhi Gupta, Deepak Singh, Shivangi Kumar, Gyanendra |
author_sort | Ahuja, Upasana S |
collection | PubMed |
description | AIM: To make dentists and pedodontists aware of a possible outcome of a rapidly growing swelling. BACKGROUND: Ewing's sarcoma is a rare aggressive variant of small round cell tumors and is an uncommon malignancy that occurs usually in childhood. It constitutes 10–15% of all primary malignant tumors and represents the second most common malignant bone tumor occurring in children and young adults. CASE DESCRIPTION: We report a case of Ewing's sarcoma in an 11-year-old male child who reported with a rapidly progressing swelling in the left mandibular posterior region. Panoramic view and computed tomography showed characteristic moth eaten and sun-ray appearance. Fine-needle aspiration cytology revealed a small round cell tumor. Since the exact diagnosis is hard to achieve before biopsy, the condition poses a difficult diagnostic dilemma for the clinician. Histopathology was performed for the accurate diagnosis. CONCLUSION: Dentists and pedodontists should develop a high index of suspicion in diagnosing cases with rapidly enlarging intraoral or extraoral swellings as early and correct diagnosis may improve clinical management and survival for patients with this disease. CLINICAL SIGNIFICANCE: Our case report is an attempt to help the dental community in developing familiarity with the clinical presentation of Ewing's sarcoma. HOW TO CITE THIS ARTICLE: Ahuja US, Puri N, Gupta D, et al. Ewing's Sarcoma of Mandible: A Case Report with Review. Int J Clin Pediatr Dent 2019;12(5):470–474. |
format | Online Article Text |
id | pubmed-7229355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-72293552020-05-21 Ewing's Sarcoma of Mandible: A Case Report with Review Ahuja, Upasana S Puri, Nidhi Gupta, Deepak Singh, Shivangi Kumar, Gyanendra Int J Clin Pediatr Dent Case Report AIM: To make dentists and pedodontists aware of a possible outcome of a rapidly growing swelling. BACKGROUND: Ewing's sarcoma is a rare aggressive variant of small round cell tumors and is an uncommon malignancy that occurs usually in childhood. It constitutes 10–15% of all primary malignant tumors and represents the second most common malignant bone tumor occurring in children and young adults. CASE DESCRIPTION: We report a case of Ewing's sarcoma in an 11-year-old male child who reported with a rapidly progressing swelling in the left mandibular posterior region. Panoramic view and computed tomography showed characteristic moth eaten and sun-ray appearance. Fine-needle aspiration cytology revealed a small round cell tumor. Since the exact diagnosis is hard to achieve before biopsy, the condition poses a difficult diagnostic dilemma for the clinician. Histopathology was performed for the accurate diagnosis. CONCLUSION: Dentists and pedodontists should develop a high index of suspicion in diagnosing cases with rapidly enlarging intraoral or extraoral swellings as early and correct diagnosis may improve clinical management and survival for patients with this disease. CLINICAL SIGNIFICANCE: Our case report is an attempt to help the dental community in developing familiarity with the clinical presentation of Ewing's sarcoma. HOW TO CITE THIS ARTICLE: Ahuja US, Puri N, Gupta D, et al. Ewing's Sarcoma of Mandible: A Case Report with Review. Int J Clin Pediatr Dent 2019;12(5):470–474. Jaypee Brothers Medical Publishers 2019 /pmc/articles/PMC7229355/ /pubmed/32440057 http://dx.doi.org/10.5005/jp-journals-10005-1665 Text en Copyright © 2019; Jaypee Brothers Medical Publishers (P) Ltd. © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Ahuja, Upasana S Puri, Nidhi Gupta, Deepak Singh, Shivangi Kumar, Gyanendra Ewing's Sarcoma of Mandible: A Case Report with Review |
title | Ewing's Sarcoma of Mandible: A Case Report with Review |
title_full | Ewing's Sarcoma of Mandible: A Case Report with Review |
title_fullStr | Ewing's Sarcoma of Mandible: A Case Report with Review |
title_full_unstemmed | Ewing's Sarcoma of Mandible: A Case Report with Review |
title_short | Ewing's Sarcoma of Mandible: A Case Report with Review |
title_sort | ewing's sarcoma of mandible: a case report with review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229355/ https://www.ncbi.nlm.nih.gov/pubmed/32440057 http://dx.doi.org/10.5005/jp-journals-10005-1665 |
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