Abstract
Synovial sarcoma is a rare mesenchymal tumour with the worst prognosis among soft tissue tumours. Although chemosensitive, it can only be cured by complete surgical resection, often limited by its anatomical relations. We present a patient with a cervical synovial sarcoma. Three operations were performed followed by equal recurrences.
Declaration of interest:
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.