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A case of a pulmonary mucosa‐associated lymphoid tissue lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar)

机译:一种肺粘膜相关淋巴组织淋巴瘤,具有染色体畸变(49,XX,+ 3,+ I(6)(P10),+ MAR)

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We report a case of a primary pulmonary mucosa‐associated lymphoid tissue (MALT) lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar). A 59‐year‐old woman was referred to our hospital for an abnormal chest shadow detected during a routine health check‐up in 2014. Chest computed tomography revealed a 3.2‐?×?2.3‐?×?2.0‐cm tumour shadow in the right middle lobe. Transbronchial biopsy did not result in the diagnosis of the tumour. Accordingly, as the tumour could have been malignant, right middle lobectomy was performed via video‐assisted thoracic surgery. On the basis of the results of immunohistochemical staining and gene analysis, the tumour was diagnosed as a primary pulmonary MALT lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar).
机译:我们举报了一种初级肺粘膜相关淋巴组织(麦芽)淋巴瘤,染色体畸变(49,XX,+ 3,+ I(6)(P10),+ MAR)。一名59岁的女子被介绍了我们的医院,在2014年在常规健康检查期间检测到的异常胸部阴影。胸部计算断层扫描显示3.2-?×2.3-?×2. 2.0厘米肿瘤阴影右中叶。跨界活检不会导致肿瘤的诊断。因此,随着肿瘤可能是恶性的,通过视频辅助胸部手术进行右中杆菌术。在免疫组织化学染色和基因分析的基础上,肿瘤被诊断为具有染色体畸变(49,XX,+ 3,+ I(6)(P10),+ MAR)的初级肺麦芽淋巴瘤。

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