Tian Panwen, Wang Ye, Wan Chun, Shen Yongchun, Wen Fuqiang
Department of Respiratory and Critical Care Medicine, West China Hospital of Sichuan University Chengdu 610041, China.
Int J Clin Exp Pathol. 2015 Feb 1;8(2):2074-8. eCollection 2015.
We represent a rare case of lung adenocarcinoma accompanied by extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT). The patient was a 66-year-old male presented with 1 month history of recurrent cough and hemoptysis. Chest CT showed solitary ground-glass opacity (GGO) in the upper lobe of the right lung and mediastinal lymph node enlargement in station 3p. A CT-guided transthoracic needle biopsy was performed. Tissue specimens of the GGO revealed a typical adenocarcinoma. Histopathologic diagnosis of mediastinal lymph node was extranodal marginal zone lymphoma of MALT. Because of its rarity, extranodal marginal zone lymphoma of MALT should be considered in the differential diagnosis when we encounter mediastinal lymphadenopathy in patients with lung adenocarcinoma.
我们报告了一例罕见的肺腺癌合并黏膜相关淋巴组织(MALT)结外边缘区淋巴瘤的病例。患者为一名66岁男性,有1个月的反复咳嗽和咯血病史。胸部CT显示右肺上叶孤立性磨玻璃影(GGO)及3p区纵隔淋巴结肿大。进行了CT引导下经胸针吸活检。GGO的组织标本显示为典型腺癌。纵隔淋巴结的组织病理学诊断为MALT结外边缘区淋巴瘤。由于其罕见性,当我们遇到肺腺癌患者出现纵隔淋巴结肿大时,在鉴别诊断中应考虑MALT结外边缘区淋巴瘤。