Conclusion
Primary Ewing’s sarcoma of the thoracic spine is an extremely rare
tumor. It is a challenging disease not only to treat but also to
diagnosis. A high index of suspicion is needed in patients who present
with few or non-specific symptoms. Early diagnosis is essential to
obtain better results and improve prognosis. In localized forms of the
tumor multi modal treatment involving neo-adjuvant chemotherapy, en bloc
vertebrectomy and adjuvant radiotherapy and chemotherapy is required for
patient outcome and satisfactory quality of life.