首页 | 本学科首页   官方微博 | 高级检索  
     

胃肠道炎性肌纤维母细胞瘤研究进展
引用本文:曾祥宇,张鹏,高金波,刘炜圳,帅晓明,陶凯雄. 胃肠道炎性肌纤维母细胞瘤研究进展[J]. 腹部外科, 2017, 30(2). DOI: 10.3969/j.issn.1003-5591.2017.02.019
作者姓名:曾祥宇  张鹏  高金波  刘炜圳  帅晓明  陶凯雄
作者单位:华中科技大学同济医学院附属协和医院胃肠外科,武汉,430022
基金项目:国家自然科学基金,武汉市科技局基金
摘    要:胃肠道炎性肌纤维母细胞瘤(inflammatory myofibroblastic tumor,IMT)是一种特殊而少见的间叶性肿瘤,发病部位主要位于胃和回盲部,常见于学龄前儿童及青少年,女性多发,临床表现无特异,术前诊断困难,确诊需依据术后病理及免疫组织化学,一般预后良好,偶有复发。本文就胃肠道IMT的临床表现、病理检查及免疫组织化学特点、诊断及鉴别诊断、治疗及预后等作一综述。

关 键 词:炎性肌纤维母细胞瘤  诊断  治疗  预后

Advances in inflammatory myofibroblastic tumor of gastrointestinal tract
Zeng Xiangyu,Zhang Peng,Gao Jinbo,Liu Weizhen,Shuai Xiaoming,Tao Kaixiong. Advances in inflammatory myofibroblastic tumor of gastrointestinal tract[J]. Journal of Abdominal Surgery, 2017, 30(2). DOI: 10.3969/j.issn.1003-5591.2017.02.019
Authors:Zeng Xiangyu  Zhang Peng  Gao Jinbo  Liu Weizhen  Shuai Xiaoming  Tao Kaixiong
Abstract:Inflammatory myofibroblastic tumor (IMT) of gastrointestinal tract is a peculiar and rare kind of tumors from mesenchymal tissue.It mainly occurs in stomach and ileocecum and is more likely associated with preschool children as well as youngsters,showing slight female predominance.The clinical manifestations of gastrointestinal IMT are not specific so that preoperative diagnosis is very difficult.Diagnosis depends on the pathological and histological examinations and usually has favorable prognosis,occasional relapse may happen however.This review discussed the clinicopathological and immunohistochemical characteristics,diagnosis and differential diagnosis,treatment and prognosis of gastrointestinal IMT.
Keywords:Inflammatory myofibroblastic tumor  Diagnosis  Treatment  Prognosis
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号