Primary Mediastinal Synovial Sarcoma

Hyunju Lee, Jin-Haeng Chung, J. Joh, Jae Ho Lee, Tae Jeong Kim, S. Jheon, S. Bang, J. Kim
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引用次数: 2

Abstract

We report a rare case of a primary mediastinal synovial sarcoma. A 44-year-old man had a well-defined tumor in the left posterior mediastinum involving the left lower lobe of the lung, as detected on chest computed tomography, and underwent an en bloc excision and a left lower lobectomy. Grossly, the tumor measured 8.0 cm in the greatest diameter, with a solid and tan-white cut surface. Histologically, the tumor was mainly composed of spindle-shaped cells with a few foci of epithelial differentiation. Immunohistochemical studies were focally positive for cytokeratin, and diffusely positive for vimentin and bcl-2. Epithelial membrane antigen, S-100 protein, desmin, smooth muscle actin, calretinin, and CD34 were all negative. The SYT-SSX1 gene fusion transcript was detected by a reverse transcription- polymerase chain reaction, which was diagnostic of primary synovial sarcoma of the mediastinum. We also reviewed the literature with regard to the clinicopathologic, immunohistochemical, and molecular studies of primary intrathoracic synovial sarcoma. (J Lung Cancer 2008;7(1):29�� 33)
原发性纵隔滑膜肉瘤
我们报告一例罕见的原发性纵隔滑膜肉瘤。一名44岁男性患者在胸部计算机断层扫描中发现左侧后纵隔有一个明确的肿瘤,累及左肺下叶,并接受了整体切除和左肺下叶切除术。肉眼可见,肿瘤最大直径为8.0 cm,切面实心,呈棕白色。组织学上,肿瘤主要由梭形细胞组成,有少量上皮分化灶。免疫组化研究显示细胞角蛋白局部阳性,而vimentin和bcl-2弥漫性阳性。上皮膜抗原、S-100蛋白、desmin、平滑肌肌动蛋白、calretinin、CD34均为阴性。通过逆转录聚合酶链反应检测SYT-SSX1基因融合转录物,用于原发性纵隔滑膜肉瘤的诊断。我们也回顾了关于原发性胸内滑膜肉瘤的临床病理、免疫组织化学和分子研究的文献。[J] .肺癌杂志;2008;7(1):29 - 33。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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