Synovial Sarcoma of the Spine: A Report of Three Cases
Author Information
Author(s): Puffer Ross C., Daniels David J., Giannini Caterina, Pichelmann Mark A., Rose Peter S., Clarke Michelle J.
Primary Institution: Mayo Clinic
Conclusion
Spinal synovial sarcoma is rare and challenging to treat, with limited long-term outcome data available.
Supporting Evidence
- All three cases involved the paraspinal muscles and spinal nerve roots.
- Two cases initially underwent smaller operations thinking the lesions were benign.
- One case had significant leptomeningeal involvement.
Takeaway
Synovial sarcoma is a rare type of cancer that can occur in the spine, and it can be hard to diagnose and treat. The best approach is usually surgery followed by chemotherapy and radiation.
Methodology
The study involved a review of medical records and a literature search for reported cases of spinal synovial sarcoma.
Limitations
The limited number of cases makes it difficult to quantify long-term outcomes for spinal synovial sarcoma.
Participant Demographics
Three patients diagnosed with spinal synovial sarcoma, including two women aged 54 and 32, and one woman aged 59.
Digital Object Identifier (DOI)
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