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Ewing Sarcoma of the External Ear Canal

Background. Ewing sarcoma (ES) is a high-grade malignant tumor that has skeletal and extraskeletal forms and consists of small round cells. In the head and neck region, reported localization of extraskeletal ES includes the larynx, thyroid gland, submandibular gland, nasal fossa, pharynx, skin, and...

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Autores principales: Binnetoglu, Adem, Baglam, Tekin, Tokuc, Gulnur, Kecelioglu Binnetoglu, Kiymet, Gerin, Fatma, Sari, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904079/
https://www.ncbi.nlm.nih.gov/pubmed/27313930
http://dx.doi.org/10.1155/2016/6925234
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author Binnetoglu, Adem
Baglam, Tekin
Tokuc, Gulnur
Kecelioglu Binnetoglu, Kiymet
Gerin, Fatma
Sari, Murat
author_facet Binnetoglu, Adem
Baglam, Tekin
Tokuc, Gulnur
Kecelioglu Binnetoglu, Kiymet
Gerin, Fatma
Sari, Murat
author_sort Binnetoglu, Adem
collection PubMed
description Background. Ewing sarcoma (ES) is a high-grade malignant tumor that has skeletal and extraskeletal forms and consists of small round cells. In the head and neck region, reported localization of extraskeletal ES includes the larynx, thyroid gland, submandibular gland, nasal fossa, pharynx, skin, and parotid gland, but not the external ear canal. Methods. We present the unique case of a 2-year-old boy with extraskeletal ES arising from the external ear canal, mimicking auricular hematoma. Results. Surgery was performed and a VAC/IE (vincristine, adriamycin, cyclophosphamide alternating with ifosfamide, and etoposide) regimen was used for adjuvant chemotherapy for 12 months. Conclusion. The clinician should consider extraskeletal ES when diagnosing tumors localized in the head and neck region because it may be manifested by a nonspecific clinical picture mimicking common otorhinolaryngologic disorders.
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spelling pubmed-49040792016-06-16 Ewing Sarcoma of the External Ear Canal Binnetoglu, Adem Baglam, Tekin Tokuc, Gulnur Kecelioglu Binnetoglu, Kiymet Gerin, Fatma Sari, Murat Case Rep Otolaryngol Case Report Background. Ewing sarcoma (ES) is a high-grade malignant tumor that has skeletal and extraskeletal forms and consists of small round cells. In the head and neck region, reported localization of extraskeletal ES includes the larynx, thyroid gland, submandibular gland, nasal fossa, pharynx, skin, and parotid gland, but not the external ear canal. Methods. We present the unique case of a 2-year-old boy with extraskeletal ES arising from the external ear canal, mimicking auricular hematoma. Results. Surgery was performed and a VAC/IE (vincristine, adriamycin, cyclophosphamide alternating with ifosfamide, and etoposide) regimen was used for adjuvant chemotherapy for 12 months. Conclusion. The clinician should consider extraskeletal ES when diagnosing tumors localized in the head and neck region because it may be manifested by a nonspecific clinical picture mimicking common otorhinolaryngologic disorders. Hindawi Publishing Corporation 2016 2016-05-30 /pmc/articles/PMC4904079/ /pubmed/27313930 http://dx.doi.org/10.1155/2016/6925234 Text en Copyright © 2016 Adem Binnetoglu 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
Binnetoglu, Adem
Baglam, Tekin
Tokuc, Gulnur
Kecelioglu Binnetoglu, Kiymet
Gerin, Fatma
Sari, Murat
Ewing Sarcoma of the External Ear Canal
title Ewing Sarcoma of the External Ear Canal
title_full Ewing Sarcoma of the External Ear Canal
title_fullStr Ewing Sarcoma of the External Ear Canal
title_full_unstemmed Ewing Sarcoma of the External Ear Canal
title_short Ewing Sarcoma of the External Ear Canal
title_sort ewing sarcoma of the external ear canal
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904079/
https://www.ncbi.nlm.nih.gov/pubmed/27313930
http://dx.doi.org/10.1155/2016/6925234
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