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作 者:许逸风 邓闻宣 李钰 尹列芬[1] Xu Yifeng;Deng Wenxuan;Li Yu(Department of Hematology,Second Affiliated Hospital of Kunming Medical University,Kunming,Yunnan,650101,China)
机构地区:[1]昆明医科大学第二附属医院血液科,云南昆明650101
出 处:《黑龙江医学》2024年第7期895-896,F0003,共3页Heilongjiang Medical Journal
摘 要:胃肠道是淋巴瘤最常见侵犯的结外部位,但原发性胃肠道淋巴瘤(PGL)却是相对少见的,根据临床亚型的不同,其组织学形态、免疫反应和分子遗传学方面存在着显著异质性,其镜下表现、治疗方法、预后也各有不同。据查阅文献得知原发性胃肠道淋巴瘤目前尚无标准的诊断方法、治疗方案,未来应完善对PGL临床亚型的分类,探索适宜的治疗方案,提高患者的预后年限。The gastrointestinal tract is the most common extranodal site invaded by lymphomas;however,primary gastrointestinal lymphomas(PGLs)are relatively rare,with significant heterogeneity in histologic morphology,immune response,and molecular genetics depending on the clinical subtype,as well as variations in microscopic manifestations,therapeutic approaches,and prognosis.According to the review of the literature,it is known that there is no standard diagnostic method or treatment plan for primary gastrointestinal lymphoma,and in the future,the classification of clinical subtypes of PGL should be improved,and appropriate treatment plans should be explored to improve the prognostic years of patients.
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