[摘要]目的探索炎症性肌纤维母细胞瘤(IMT)的临床病理特征。方法 回顾性分析2006年1月-2010年1月10例炎症性肌纤维母细胞瘤患者的临床及病理形态学资料，进行免疫组织化学分析。结果 10例患者3例位于颈或胸腹壁软组织，4例位于肺，另3例位于肠系膜或网膜，均经手术治疗恢复良好。随访6-56个月，1例复发，1例转移。结论 炎症性肌纤维母细胞瘤是以炎症为背景、肌纤维母细胞增生为主的一种少见的良性肿瘤，具有一定的复发倾向及恶变潜能。确诊依靠病理，手术为主要治疗手段。术后需对患者密切随访。

    [关键词]炎症性肌纤维母细胞瘤； 病理特征； 免疫组织化学

    [中图分类号]R361+.3[文献标识码]A [文章编号] 1005-0515(2010)-12-011-01

    Drug instructions for clinical nursing in the hepatobiliary surgery department

    JIANG Ying,YANG Yan-ying,HE Run,DAN Hui-fang,WEI Ji-hong.

    (Mianyang Central Hospital,Sichuan Province,Mianyang,621000 China)

    [Abstract]ObjectiveExplore inflammatory myofibroblasts cell tumor (IMT) the clinical and pathological features.Methods Retrospective analysesJanuary 2006 to January 2010 theclinical and pathological morphology material of10 cases the inflammatory myofibroblasts cell tumor patients ,proceed immunohistochemistry analysis.The resultsAt 10 patients ,3 cases in the neck or chest abdominal wall soft tissue, 4 cases in the lung, other 3 cases were located in the mesenteric or retinal, all by surgical treatment of a good recovery .Follow-up visit 6-56 months, 1 cases relapse, 1 case of transfer.conclusionInflammatory myofibroblasts cell tumor is a rare benign tumor for inflammation in the background, myofibroblasts cell hyperplasia primarily recurrence, has certain tendencies and m alignant transformation potential. A correct diagnosis depends on Pathological, surgery as the main therapy. Postoperative patients need to close follow-up. ......