[A case of extramedullary plasmacytoma of the lung diagnosed by video-assisted thoracic surgery].

Takeshi Osawa, Kenzo Yuyama, Takashi Takahashi, Yusuke Tsubouchi, Kenichiro Egawa, Hisanori Matsushita
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Abstract

A 69-year-old man who had had a history of abnormal chest radiograph was admitted. Chest computed tomography showed an 18 x 18 mm apparently-circumscribed mass in the right posterior-basal segment. We performed right lower lobe wedge resection via video-assisted thoracic surgery to establish a definitive diagnosis. The mass was an apparently-circumscribed, gray and solid tumor, the microscopic findings of which included diffuse proliferation of plasma cells with an abnormal profile. Immunohistochemical staining revealed IgG-kappa light chain monoclonality. Absence of M protein in the serum and urine was confirmed. Bone-marrow puncture and positron-emission tomography revealed normal findings. Thus a diagnosis of extramedullary plasmacytoma (EMP) of the lung was made. We report trends of the immunoglobulin isotype of EMP in Japan. Since it has been reported that some of the cases in EMP progress to multiple myeloma (MM), careful observation and follow-up is needed hereafter. In the present case, no recurrence or progress to MM was observed within the first year after surgery.

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[电视胸外科诊断肺髓外浆细胞瘤1例]。
一位69岁男性,有异常胸片病史。胸部计算机断层扫描显示右侧后基底段有一个18 × 18 mm的明显边界肿块。我们通过电视辅助胸外科手术进行右下肺叶楔形切除以确定明确的诊断。肿块为界限分明的灰色实体瘤,镜下见浆细胞弥漫性增生,形态异常。免疫组化染色显示IgG-kappa轻链单克隆。血清和尿液中均无M蛋白。骨髓穿刺和正电子发射断层扫描显示正常。因此诊断为肺髓外浆细胞瘤。我们报告了日本EMP免疫球蛋白同型的趋势。由于有报道称部分EMP发展为多发性骨髓瘤(MM),因此需要仔细观察和随访。在本病例中,在手术后的第一年没有观察到复发或进展为MM。
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