Comprehensive treatment of primary pelvic synovial sarcoma: A 28-month follow-up case report and review of the literature.

ABSTRACT:

Background

Primary synovial sarcoma originating in the pelvis is an extremely rare malignancy, and only a few cases have been reported. Usually, the tumor is detected at an advanced stage, making treatment more difficult. Lacking high-quality research, there are no consensus guidelines for the systemic treatment of the disease.

Case presentation

We admitted a 32-year-old male patient with an MRI suggestive of an 8.2 × 7.7 x 8.9 cm mass in the pelvis with bleeding. After a comprehensive evaluation, the patient underwent surgery, and postoperative pathology suggested biphasic synovial sarcoma. Once the diagnosis was clear, the patient was treated with chemotherapy, radiotherapy, and targeted therapy. Unfortunately, the patient died due to a recurrence of pelvic synovial sarcom

SUBMITTER: Li Z 

PROVIDER: S-EPMC11489358 | biostudies-literature | 2024 Oct

REPOSITORIES: biostudies-literature