Publication:
Ewing Sarcoma of the External Ear Canal

dc.contributor.authorBİNNETOĞLU, ADEM
dc.contributor.authorTOKUÇ, AYŞE GÜLNUR
dc.contributor.authorsBinnetoglu, Adem; Baglam, Tekin; Tokuc, Gulnur; Binnetoglu, Kiymet Kecelioglu; Gerin, Fatma; Sari, Murat
dc.date.accessioned2022-03-14T08:14:39Z
dc.date.accessioned2026-01-10T18:43:13Z
dc.date.available2022-03-14T08:14:39Z
dc.date.issued2016
dc.description.abstractBackground. 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.
dc.identifier.doi10.1155/2016/6925234
dc.identifier.eissn2090-6773
dc.identifier.issn2090-6765
dc.identifier.pubmed27313930
dc.identifier.urihttps://hdl.handle.net/11424/241266
dc.identifier.wosWOS:000378311900001
dc.language.isoeng
dc.publisherHINDAWI LTD
dc.relation.ispartofCASE REPORTS IN OTOLARYNGOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectROUND-CELL TUMORS
dc.subjectADULTS
dc.subjectFAMILY
dc.titleEwing Sarcoma of the External Ear Canal
dc.typearticle
dspace.entity.typePublication
oaire.citation.titleCASE REPORTS IN OTOLARYNGOLOGY
oaire.citation.volume2016

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