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颈部炎性肌纤维母细胞瘤1例报告并文献复习
引用本文:陈少全,陈煌辉,王烈,钱之远,林瑞娇.颈部炎性肌纤维母细胞瘤1例报告并文献复习[J].中国误诊学杂志,2008,8(23):5551-5553.
作者姓名:陈少全  陈煌辉  王烈  钱之远  林瑞娇
作者单位:南京军区福州总医院普外科,福建,福州,350025
摘    要:目的:提高对颈部炎性肌纤维母细胞瘤的认识。方法:通过对1例颈部炎性肌纤维母细胞瘤的临床资料进行分析,并复习国内外相关文献。结果:炎性肌纤维母细胞瘤是一种间叶性肿瘤,由分化的肌纤维母细胞性梭形细胞组成,常伴有大量浆细胞和(或)淋巴细胞。免疫组化vimentin、SMactin常呈强阳性表达。术后随访1 a无复发。结论:颈部炎性肌纤维母细胞瘤在临床上是一种罕见的肿瘤,其确诊主要依靠病理组织学,治疗以根治性手术为首选。

关 键 词:肿瘤  肌组织/诊断  头颈部肿瘤/诊断  病例报告  人类

Inflammatory Myofibroblastic Tumor of Neck:A Case Report and Literature Review
Institution:CHEN Shao-quan,CHEN Huang-hui,QIAN Zhi-yuan,et al. (General Surgery.Fuzhou General Hospital of Nanjing Military Region ,Fuzhou 350025 ,China)
Abstract:Objective:To improve the recongnization of neck inflammatory myofibroblastic tumor. Methods:The clinical data of one case of neck inflammatory myofibroblastic tumor was analyzed and the related literature was reviewed. Results : Inflammatory mvofibroblastic tumor was a mesenchvmal neoplasm composed of transformed myofibroblastic spindle cells with infitration of a large number of inflammatory ceiland/or lymphocytes. The immunohistochemistry of Vimentin. smactin expression often showed strongly. There wasn't recurrence by one year follow-up. Conclusion:Neck inflammatory myofibroblastic tumor is a rare tumor. The definitive diagnosis of inflammatory myofibroblastic tumor depended on cytology of adrenal tissue.radical surgery is the first choice.
Keywords:Neoplasms  Muscle Tissue/diagnosis: Head and Neck Neoplasms/diagnosis  Case Reports [Publication Type2  Humans
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