Abstract
Ewing’s sarcoma most commonly occurs in bone and only very rarely in the extradural spinal canal. Herein, we present the clinical course, diagnosis, and treatment of a 6-year-old girl admitted with a complaint of strength loss in her right lower extremity. Magnetic resonance imaging revealed an extradural spinal canal tumor extending from level T2 to T5; she underwent laminectomy. The histopathological, immunohistochemical, and molecular cytogenetic data were compatible with Ewing’s sarcoma. We detected no malignant focus on postoperative staging work-up and prescribed postoperative radiotherapy and chemotherapy. A brief review of the literature on primary extradural extraosseous Ewing’s sarcoma of the spinal canal is presented.
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