Yoon G S, Park S Y, Kang G H, Kim O J
Department of Diagnostic Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Korean Med Sci. 1998 Feb;13(1):71-6. doi: 10.3346/jkms.1998.13.1.71.
We report an unusual primary case of pulmonary sarcoma that developed in the lung of a 36-year-old woman. The tumor had histologic, immunologic and ultrastructural features identical to those of biphasic synovial sarcoma of the soft tissue. It consisted of an intimate admixture of cytokeratin and epithelial membrane antigen(EMA)-positive neoplastic epithelial cells and vimentin-positive fibroblast-like spindle cells with areas of hyalinization. The patient had a lobectomy and showed no evidence of recurrence or tumor at other sites 15 months after surgery. This case is an useful addition to the small number of published reports on pulmonary synovial sarcoma. The distinctive features of this neoplasm allow it to be different from other types of primary and metastatic malignancies in the lung.
我们报告了一例罕见的原发性肺肉瘤病例,发生在一名36岁女性的肺部。该肿瘤具有与软组织双相滑膜肉瘤相同的组织学、免疫学和超微结构特征。它由细胞角蛋白和上皮膜抗原(EMA)阳性的肿瘤上皮细胞与波形蛋白阳性的成纤维细胞样梭形细胞紧密混合组成,并有玻璃样变区域。患者接受了肺叶切除术,术后15个月未发现复发迹象或其他部位有肿瘤。该病例为已发表的少数关于肺滑膜肉瘤的报告增添了新内容。这种肿瘤的独特特征使其有别于肺部其他类型的原发性和转移性恶性肿瘤。