Extraskeletal Ewing Sarcoma: Report of an Extremely Rare Case in Temporal Region
AbstractExtraskeletal Ewing sarcoma (EES) is an uncommon tumor with low prevalence in the head and neck region. Herein, we report a 13-year-old boy with EES in the temporal region, which was managed by surgery and chemotherapy. The histological characteristics and the clinical manifestations of the lesion and our surgical approach will be discussed as well.
Cotterill S, Ahrens S, Paulussen M, Jurgens H, Voute P, Gadner H, Craft A. Prognostic factors in Ewing’s tumor of bone: analysis of 975 patients from the European Intergroup Cooperative Ewing’s Sarcoma Study Group. J clin oncol
Ali S, Mackenzie K, Reid R, O'Neill G, Ganly I. Cervical extraskeletal Ewing's sarcoma: case report demonstrating radiological features and management. J Laryngol & Otol
Kinsella TJ, Triche T, Dickman P, Costa J, Tepper J, Glaubiger D. Extraskeletal Ewing's sarcoma: results of combined modality treatment. J clin oncol
Hafezi S, Seethala RR, Stelow EB, Mills SE, Leong IT, MacDuff E, Hunt JL, Perez-Ordoñez B, Weinreb I. Ewing’s family of tumors of the sinonasal tract and maxillary bone. Head neck pathol
Windfuhr JP. Primitive neuroectodermal tumor of the head and neck: incidence, diagnosis, and management. Ann Otol Rhinol Laryngol