Authors : G. V. Ramachandra Reddy, Swati Surushe, Saumya Khare, Md. Ishtiyak Khan, Sadiya Tarannum, Shubhi Maheshwari
DOI : 10.18231/j.jooo.2022.045
Volume : 8
Issue : 4
Year : 2022
Page No : 215-220
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 after osteosarcoma - with an estimated incidence of 2.93 cases/million inhabitants under 20 years of age/year. This paper presents a case of 10-year-old male child who reported with a rapidly progressing swelling in the right mandibular posterior ramus region. The patient was diagnosed with Ewing’s sarcoma on the basis of history, clinical, radiological and confirmed with histopathological & immunohistochemical examination. Since the exact diagnosis is hard to achieve before biopsy, the condition poses a difficult diagnostic dilemma for the clinician.
Keywords: Ewing's sarcoma, Mandible, Primitive neuroectodermal tumor.