[模仿晚期肺癌的原发性肺弥漫大 B 细胞淋巴瘤:病例报告】。]

Q4 Medicine
Daisuke Ito, Hitoshi Suzuki, Shin Shomura
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引用次数: 0

摘要

原发性肺弥漫大B细胞淋巴瘤(DLBCL)非常罕见,占所有恶性淋巴瘤的0.4%至1.0%,占所有肺部恶性肿瘤的0.45%。我们报告了一例由甲氨蝶呤相关淋巴组织增生性疾病(MTX-LPD)引起的原发性肺DLBCL。一名 73 岁的男性因肺部结节不断增大而转诊至我院。经支气管镜活检未能确诊,但正电子发射计算机断层扫描(PET-CT)显示同一区域的SUVmax为28.7,对侧纵隔的SUVmax为40.5,提示为晚期原发性肺癌。我科为患者实施了胸腔镜下左肺下叶部分切除术。组织病理学检查显示 AE1/AE3 阴性,CD20 和 79a 阳性,bcl-2 阳性,诊断为原发性肺 DLBCL。怀疑是MTX-LPD,停药后残留肿瘤缩小。如果无法通过经支气管镜对不断扩大的结节阴影进行活检来确诊,则应考虑进行积极的手术诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Primary Pulmonary Diffuse Large B-cell Lymphoma Mimics Advanced Lung Cancer:Report of a Case].

Primary pulmonary diffuse large B-cell lymphoma( DLBCL) is rare, accounting for 0.4% to 1.0% of all malignant lymphomas and 0.45% of all lung malignancies. We report a case of primary pulmonary DLBCL caused by methotrexate-associated lymphoproliferative disorder (MTX-LPD). A 73-year-old man was referred to our hospital due to a growing lung nodule. Transbronchoscopic biopsy did not confirm the diagnosis, but positron emission tomography-computed tomography (PET-CT) showed an accumulation of SUVmax 28.7 in the same area and SUVmax 40.5 in the contralateral mediastinum, suggesting an advanced primary lung cancer. A partial thoracoscopic left lower lobe resection was performed in our department. Histopathological examination revealed AE1/AE3 negative, CD20 and 79a positive, bcl-2 positive, and a diagnosis of primary lung DLBCL. MTX-LPD was suspected, and discontinuation of the drug resulted in subsequent shrinkage of the residual tumor. If the diagnosis cannot be made by transbronchoscopic biopsy of an expanding nodule shadow, aggressive surgical diagnosis should be considered.

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