Navas-Palacios J J, Colina-Ruizdelgado F, Sanchez-Larrea M D, Cortes-Cansino J
Cancer. 1983 May 1;51(9):1682-90. doi: 10.1002/1097-0142(19830501)51:9<1682::aid-cncr2820510921>3.0.co;2-p.
Seven cases of inflammatory fibroid polyp (IFP) are studied, two of them with electron microscopy. The morphologic findings suggest a myofibroblastic origin for the proliferating cells. Other histogenetic hypothesis which propose a neural or vascular nature for this lesion are ruled out. The ultrastructural features of the proliferating cells are different from schwann and endothelial cell tumors. Moreover, the immunohistochemical technique to detect Factor VIII related antigen was negative in the intercapillary cells of the seven cases. Our conclusion is that inflammatory fibroid polyp of the gastrointestinal tract represent a reactive lesion of myofibroblastic nature.
对7例炎性纤维性息肉(IFP)进行了研究,其中2例进行了电子显微镜检查。形态学结果提示增殖细胞起源于肌成纤维细胞。其他提出该病变具有神经或血管性质的组织发生假说被排除。增殖细胞的超微结构特征与施万细胞瘤和内皮细胞瘤不同。此外,检测因子VIII相关抗原的免疫组织化学技术在7例的毛细血管间细胞中呈阴性。我们的结论是,胃肠道炎性纤维性息肉是一种肌成纤维细胞性质的反应性病变。