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原发性肺滑膜肉瘤需与胫骨造釉细胞瘤肺转移相鉴别:1例报告

Primary pulmonary synovial sarcoma requiring differentiation from pulmonary metastasis of tibial adamantinoma: a case report.

作者信息

Shirai Toshiharu, Tsuchida Shinji, Terauchi Ryu, Mizoshiri Naoki, Konishi Eiichi, Tomita Yasuhiko, Shimada Junichi, Fujiwara Hiroyoshi, Kubo Toshikazu

机构信息

Department of Orthopaedics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan.

出版信息

BMC Res Notes. 2014 Oct 18;7:736. doi: 10.1186/1756-0500-7-736.

Abstract

BACKGROUND

Primary pulmonary synovial sarcoma (PPSS) is rare. We describe a case of PPSS complicated by tibial adamantinoma that required differentiation from lung metastasis.

CASE PRESENTATION

A 39-year-old Japanese woman presented with hemoptysis, dyspnea, and a well-defined tumor measuring 3.0 cm in greatest diameter in the right lower lobe on chest computed tomography (CT). Positron emission tomography/CT with fluorodeoxyglucose (FDG-PET/CT) showed mild uptake of FDG (maximum standardized uptake value of 2.0). Her past history included surgery for adamantinoma of the right tibia at age 25 years. We considered the possibility of pulmonary metastasis from the adamantinoma and performed fluoroscopy-assisted thoracoscopic resection of the tumor after CT-guided Lipiodol marking. Histologically, the tumor was composed mainly of a dense proliferation of spindle cells. Immunohistochemical studies were positive for epithelial membrane antigen, B cell lymphoma 2, and transducing-like enhancer of split 1. They were negative for CD34. The synovial sarcoma, X breakpoint 1 gene-fusion transcript was detected by reverse transcription-polymerase chain reaction. It is diagnostic of PPSS. Resection margins were negative. The patient was well without evidence of recurrence or metastasis of the PPSS or adamantinoma at the 30-month and 15-year follow-ups.

CONCLUSION

Clinical and radiological manifestations of PPSS overlap with those of other lung tumors. The solitary pulmonary nodule in this case was indistinguishable from pulmonary metastases of the adamantinoma based on clinical symptoms, epidemiology, chest radiography, CT, and FDG-PET/CT. PPSS was diagnosed only after evaluating gross pathology, histology, immunohistochemistry, and cytogenetics. PPSS should be included in the differential diagnosis of a well-defined homogeneous round or oval lung mass. To our knowledge, this is the first report of PPSS complicated by adamantinoma.

摘要

背景

原发性肺滑膜肉瘤(PPSS)较为罕见。我们描述了一例合并胫骨造釉细胞瘤的PPSS病例,该病例需要与肺转移瘤相鉴别。

病例报告

一名39岁的日本女性,出现咯血、呼吸困难症状,胸部计算机断层扫描(CT)显示右下叶有一个边界清晰、最大直径为3.0 cm的肿瘤。氟脱氧葡萄糖正电子发射断层扫描/CT(FDG-PET/CT)显示FDG摄取轻度增高(最大标准化摄取值为2.0)。她既往有25岁时因右胫骨造釉细胞瘤接受手术的病史。我们考虑了造釉细胞瘤肺转移的可能性,并在CT引导下进行碘油标记后,通过荧光镜辅助胸腔镜切除了肿瘤。组织学上,肿瘤主要由密集增生的梭形细胞组成。免疫组织化学研究显示上皮膜抗原、B细胞淋巴瘤2和分裂样增强子1呈阳性,CD34呈阴性。通过逆转录-聚合酶链反应检测到滑膜肉瘤X断点1基因融合转录本,确诊为PPSS。手术切缘阴性。在30个月和15年的随访中,患者情况良好,无PPSS或造釉细胞瘤复发或转移的迹象。

结论

PPSS的临床和影像学表现与其他肺部肿瘤重叠。基于临床症状、流行病学、胸部X线、CT和FDG-PET/CT,该病例中的孤立性肺结节与造釉细胞瘤的肺转移难以区分。只有在评估大体病理、组织学、免疫组织化学和细胞遗传学后才能诊断PPSS。PPSS应纳入边界清晰的均匀圆形或椭圆形肺部肿块的鉴别诊断中。据我们所知,这是首例合并造釉细胞瘤的PPSS报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20bf/4210480/4ff244ad2d11/13104_2014_3260_Fig1_HTML.jpg

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