Habu S, Okamoto E, Toyosaka A, Nakai Y, Takeuchi M
First Department of Surgery, Hyogo College of Medicine, Nishinomiya, Japan.
Surg Today. 1998;28(4):401-4. doi: 10.1007/s005950050149.
Synovial sarcomas are exceedingly rare neoplasms of the digestive tract. We herein report a case of a synovial sarcoma occurring in the esophagus of a 20-year-old man. He had a history of acute lymphocytic leukemia and had undergone aggressive chemotherapy between the ages of 4 and 8 years. The tumor, which was large and extended into the upper mediastinum, was successfully resected without an esophagectomy via the cervical approach. After postoperative radiation and chemotherapy, the patient remained healthy, without any evidence of disease 20 months after the operation.
滑膜肉瘤是极为罕见的消化道肿瘤。我们在此报告一例发生于一名20岁男性食管的滑膜肉瘤病例。他有急性淋巴细胞白血病病史,在4至8岁期间接受过强化化疗。肿瘤体积较大,延伸至上纵隔,通过颈部入路成功切除,未行食管切除术。术后进行放疗和化疗后,患者保持健康,术后20个月无任何疾病迹象。