Key result
A 17-year-old female with a rare intra-articular synovial sarcoma of the hip joint was treated with neoadjuvant chemoradiation and hemipelvectomy, showing no local recurrence at 3 years.
Why the study?
Primary intra-articular synovial sarcoma is an extremely rare variant of synovial sarcoma, with only one previously published case report arising from the hip joint.
Case Report (n=1)
No
This report documents an extremely rare case of primary intra-articular synovial sarcoma in the hip joint, emphasizing the role of MRI and biopsy in diagnosing atypical joint masses.
Documents rare primary intra-articular hip synovial sarcoma; extends sparse literature but leaves optimal management open.
Synovial sarcoma is a type of soft tissue sarcoma that commonly occurs around large joints. However, primary intra-articular synovial sarcoma is considered an extremely rare variant of synovial sarcoma. We present a case of synovial sarcoma arising from the hip joint in a 17-year-old female patient. Clinical, radiographic, magnetic resonance imaging and histopathology findings are described. The patient underwent neoadjuvant chemoradiation therapy followed by right hemipelvectomy, and there was no local recurrence in the subsequent follow ups. Unfortunately, the patient had pleural metastasis, and she was treated with palliative chemotherapy. To the best of our knowledge, there is only one published case report in the English literature on intra-articular synovial sarcoma from the hip joint.
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Asiri et al. (2020) conducted a case report in Intra-articular synovial sarcoma (n=1). Neoadjuvant chemoradiation therapy and right hemipelvectomy was evaluated on Local recurrence and survival. A 17-year-old female with a rare intra-articular synovial sarcoma of the hip joint was treated with neoadjuvant chemoradiation and hemipelvectomy, showing no local recurrence at 3 years.
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