Ewing’s sarcoma is a rare malignant cancer primarily affecting children and adolescents, with fewer than 500 cases reported annually in the United States.1 Histopathologically, Ewing’s sarcoma is characterized as a poorly differentiated, small round blue cell tumor and is most commonly identified as a primary bone malignancy.2 Less frequently, Ewing’s sarcoma can present as a primary soft tissue, or extraosseous, tumor.3 Ewing’s sarcoma can occur along the spinal column as an osseous or...
