原发性十二指肠T淋巴细胞淋巴瘤病例回顾  

Case review of primary duodenal T-lymphocyte lymphoma

作　　者：白厚桥[1] 徐诗钦 BAI Hou-qiao;XU Shi-qin(Department of Gastroenterology,Qingdao University Affiliated Weihai Municipal Second Hospital,Qingdao 264200,China)

机构地区：[1]青岛大学附属威海市立第二医院消化科,264200

出　　处：《中国实用医药》2024年第11期150-152,共3页China Practical Medicine

摘　　要：原发性肠道淋巴瘤(PIL)最常见的部位是回盲部,病理类型以B细胞来源为主,其中弥漫大B细胞淋巴瘤(DLBCL)最为常见,其次是黏膜相关淋巴组织型边缘区B细胞淋巴瘤。PIL总体发病率偏低,但呈逐渐上升趋势。国内有关PIL的报道较少。现报告1例原发性十二指肠T淋巴细胞淋巴瘤。The most common site of primary intestinal lymphoma(PIL)is ileocecal region,and the pathological type is mainly derived from B cells,among which diffuse large B-cell lymphoma(DLBCL)is the most common,followed by mucosa-associated lymphoid tissue marginal zone B-cell lymphoma.Its overall incidence is low but gradually increasing.There are fewer reports about PGIL in the country.1 case of primary duodenal T lymphoma has been reported.

关 键 词：原发性肠道淋巴瘤 B细胞淋巴瘤 十二指肠 T细胞淋巴瘤 

分 类 号：R735.31[医药卫生—肿瘤]