Case of Synovial Sarcoma in a 16-Year-Old Girl
Author Information
Author(s): Zhang Jing, Li Zhengyi, Guo Guoqiang, Jin Chunchun, Deng Meifang
Primary Institution: Department of Ultrasound, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People’s Hospital, Shenzhen, China
Conclusion
Synovial sarcoma is a rare malignant tumor that requires early detection and accurate diagnosis for effective treatment.
Supporting Evidence
- Synovial sarcoma accounts for 5%–10% of malignant tumors of mesenchymal tissue.
- The patient underwent two surgical treatments and regular chemotherapy.
- Follow-up revealed bilateral lung metastases 13 months after surgery.
- Imaging tests showed a high likelihood of malignancy.
Takeaway
A 16-year-old girl had a rare type of cancer called synovial sarcoma in her thigh, which can be very serious. Doctors found it early, but it can come back or spread to other parts of the body.
Methodology
The case involved imaging features, surgical procedures, and pathological results, along with a literature review of 25 relevant case reports.
Limitations
The study is based on a single case report and literature review, which may not represent all cases of synovial sarcoma.
Participant Demographics
The patient was a 16-year-old Chinese female.
Digital Object Identifier (DOI)
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