Pulmonary Mucosa-Associated Lymphoid Tissue Lymphoma: A Report of 2 Cases and Literature Review

Xiang-ting Xie, Ying Zhang, Xiaoyan Tan, Yun Luo
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Abstract

Pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma is indolent and progresses more slowly than other malignant lymphomas. The clinical features are not specific and the diagnosis can often be difficult. Here, we present two rare cases of pulmonary MALT lymphoma. Both patients were incidentally found lesions in the lungs with chest computed tomography during physical examination. They were finally diagnosed by pathological biopsy. One received complete resection, the other was treated with chemotherapy. There were no recurrence in the two patients during follow-up. We also review relevant literature to provide a better recognition of this disease.
肺粘膜相关淋巴组织淋巴瘤2例报告并文献复习
肺粘膜相关淋巴组织淋巴瘤(MALT)是一种惰性淋巴瘤,其进展速度比其他恶性淋巴瘤慢。临床特征不明确,诊断往往很困难。在此,我们报告两例罕见的肺部MALT淋巴瘤。两例患者均在体格检查时偶然发现肺部病变。最终通过病理活检确诊。一名患者接受了完全切除,另一名患者接受了化疗。随访期间两例患者均无复发。我们也回顾了相关文献,以提供更好的认识这种疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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