Soria-Céspedes Danny, Galván-Linares Aldo Iván, Oros-Ovalle Cuauhtemoc, Gaitan-Gaona Francisco, Ortiz-Hidalgo Carlos
Department of Pathology, The American British Cowdray Medical Center, Sur 136#116. Col Las Américas, 01120, Mexico, DF, Mexico.
Head Neck Pathol. 2013 Dec;7(4):400-3. doi: 10.1007/s12105-013-0440-5. Epub 2013 Apr 7.
Synovial sarcoma (SS) arises primarily in the lower extremities with a predilection for sites in proximity to large joints, such as the knee. It rarely occurs in the head and neck region, and the tonsil is an unusual site for the tumor, with only eight previously published cases in this anatomical site. We present a case of a primary monophasic SS arising in the right tonsil in a 63-year-old male. His medical history was noncontributory. Immunohistochemistry showed that cytokeratin OSCAR, EMA, Bcl-2, vimentin, PGP 9.5, and TLE1 were diffusely positive. A molecular analysis using RT-PCR indicated that the patient was positive for the SYT/SSX1 fusion transcript. A diagnosis of monophasic synovial sarcoma of the tonsil was made.
滑膜肉瘤(SS)主要发生于下肢,尤其好发于大关节附近部位,如膝关节。它很少发生于头颈部区域,而扁桃体是该肿瘤的一个罕见发病部位,此前在这个解剖部位仅有8例报道。我们报告一例63岁男性右侧扁桃体原发性单相滑膜肉瘤病例。他的病史无特殊。免疫组化显示细胞角蛋白OSCAR、EMA、Bcl-2、波形蛋白、PGP 9.5和TLE1弥漫性阳性。采用逆转录聚合酶链反应(RT-PCR)进行的分子分析表明,该患者SYT/SSX1融合转录本呈阳性。最终诊断为扁桃体单相滑膜肉瘤。