A case of monophasic synovial sarcoma presenting as a vulvar mass |
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Authors: | Ambani Dipika S White Beverly Kaplan Alan L Alberto Ayala |
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Affiliation: | Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX 77030, USA. dambani@bcm.tmc.edu |
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Abstract: | ![]() BACKGROUND: Synovial sarcoma is the fourth most commonly occurring sarcoma, accounting for 8-10% of all sarcomas. They arise from unknown pleuripotent stem cells that are capable of differentiating into mesenchymal and/or epithelial structures. Synovial sarcoma is characterized by specific chromosomal translocation t (X; 18)(p11, q11). CASE: We report the first case of monophasic synovial sarcoma arising in soft tissues of the vulva in a 33-year-old female. Complete excision of the mass was possible with tumor-free margins. CONCLUSION: Only four previous cases of biphasic synovial sarcoma arising in the vulva have been reported. The finding of the SYT-SSX2 translocation is generally associated with a better prognosis, besides tumor negative margins after excision offer the possibility of a better outlook for this patient. |
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