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血管肌纤维母细胞瘤两例临床病理分析(3)
http://www.100md.com 2018年6月1日 《新医学》 20186
     AMF临床上较为罕见,常表现为无痛性肿块,质地软,边境清楚,似有包膜,一般直径为05~120cm,术前确诊困难,影像学检查无特异性,易被误诊,只能通过术后的病理学检查确诊,免疫组化有助于诊断。只有充分认识AMF的临床特点、病理学与免疫组化特征,才可对其作出正确诊断。AMF是一种良性的软组织肿瘤,手术切除是唯一的治疗方法,局部单纯切除后可治愈[12]。该病预后良好,少数患者会出现术后复发及恶变,宜行长期随访[13]。

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    (收稿日期:20180213), 百拇医药(汪维佳 廖志波 古建雄 陈健宁 陈冰 赖骏威 邵春奎)
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