原发性小肠淋巴瘤(Ⅰ):组织学类型及CT诊断  

Primary small intestinal lymphoma (Ⅰ):histologic type and CT diagnosis

作　　者：黄梦庭 吴林霞 刁楠[1] 韩萍[1] HUANG Mengting;WU Linxia;DIAO Nan;HAN Ping(Department of Radiology,Union Hospital,Tongji Medical College,Huazhong University of Science and Technology,Hubei Province Key Laboratory of Molecular Imaging,Wuhan 430022,China.)

机构地区：[1]华中科技大学同济医学院附属协和医院放射科,分子影像湖北省重点实验室,武汉430022

出　　处：《国际医学放射学杂志》2022年第2期210-214,223,共6页International Journal of Medical Radiology

摘　　要：原发性小肠淋巴瘤(PSIL)是指原发于十二指肠、空肠和回肠黏膜下淋巴组织的恶性肿瘤,较少见,绝大多数为非霍奇金淋巴瘤。CT肠道成像对显示小肠淋巴瘤具有重要价值。充分认识该病的临床和影像学表现是正确诊断与鉴别诊断的基础。就PSIL的临床表现、CT肠道成像检查及其影像表现进行介绍,旨在提高对该病的诊断水平。Primary small intestinal lymphoma(PSIL)is a malignant tumor originating in the submucosal lymphoid tissue of duodenum,jejunum and ileum,which is rare and mostly non-Hodgkin’s lymphoma.CT enterography is of great value in displaying small intestinal lymphoma.Understanding of the imaging features and clinical manifestations of the disease is the basis for an accurate diagnosis and differential diagnosis.In order to improve the diagnosis of PSIL,this paper introduces the clinical manifestations,CT small intestine angiography,and imaging findings of PSIL.

关 键 词：原发性小肠淋巴瘤 CT肠道成像 体层摄影术 X线计算机 

分 类 号：R735.32[医药卫生—肿瘤] R445.3[医药卫生—临床医学]