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Concurrent Gastric and Pulmonary Mucosa-Associated Lymphoid Tissue Lymphomas with Pre-Existing Intrinsic Chronic Inflammation: A Case Report and a Review of the Literature

机译:并发胃和肺粘膜相关的淋巴样组织淋巴瘤与既有的内在性慢性炎症:一例病例并文献复习

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摘要

Herein, we report a rare case of concurrent gastric and pulmonary mucosa-associated lymphoid tissue (MALT) lymphomas. A 65-year-old man who had been diagnosed with Helicobacter pylori-positive gastric MALT lymphoma received eradication therapy and achieved complete remission. During follow-up, he developed de novo pulmonary MALT lymphoma as a sequela of pulmonary tuberculosis, accompanied by recurrent gastric MALT lymphoma. Polymerase chain reaction (PCR) products of the CDR3 region of the immunoglobulin heavy chain gene showed an overall polyclonal pattern with bands at 400 base pairs (bp) and 200 bp predominant in the pulmonary tissue, as well as two distinctive bands in the gastric tissue at 400 bp and 200 bp. This case suggests that multiorgan lymphomas are more likely to be independent from each other when they are far apart, involve different organ systems, and have independent precipitating factors.
机译:在此,我们报告了罕见的并发胃和肺粘膜相关淋巴样组织(MALT)淋巴瘤的病例。一名被诊断患有幽门螺杆菌阳性胃MALT淋巴瘤的65岁男子接受了根除治疗并完全缓解。在随访期间,他从头发展了肺MALT淋巴瘤,这是肺结核的后遗症,并伴有复发性胃MALT淋巴瘤。免疫球蛋白重链基因CDR3区的聚合酶链反应(PCR)产物显示出总体多克隆模式,在肺组织中有400个碱基对(bp)和200 bp的条带,在胃组织中有两个独特的条带分别为400 bp和200 bp。这种情况表明,多器官淋巴瘤相距较远,涉及不同器官系统并具有独立的促发因素时,它们更有可能彼此独立。

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