Eversole L R, Christensen R, Ficarra G, Pierleoni L, Sapp J P
University of the Pacific School of Dentistry, San Francisco, Calif 94115, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999 Apr;87(4):471-6. doi: 10.1016/s1079-2104(99)70247-7.
Fibroblastic proliferations of the oral cavity are extremely varied, yet they share certain features-spindle cell morphology, collagen synthesis, and fasciculation. Nodular fasciitis is a cellular fibroblastic lesion, uncommonly located in the oral submucosa, that shows smooth muscle actin (SMA) immunoreactivity. Solitary fibrous tumor expresses a CD34 fibroblast phenotype. The aim of this study is to report instances of nodular fasciitis and solitary fibrous tumor in the orofacial region and investigate immunohistochemical markers to compare and contrast fibroblastic phenotypic heterogeneity in these tumors.
Seven benign cellular fibrogenic tumors initially diagnosed as nodular fasciitis over a 10-year period were examined. Immunohistochemical markers, including S-100 protein, SMA, CD68, CD34, and vimentin, were used to further characterize these lesions.
All tumors occurred in adults, and the buccal mucosa was found to be the favored site. The spindle cells in these tumors showed phenotypic heterogeneity both within and between tumors. All were vimentin-reactive and harbored small populations of CD68-positive macrophage/dendrocytes. Five tumors were SMA-positive and CD34-negative; the tumor in one case was SMA-negative and CD34-positive, and that in another was SMA-positive and CD34-positive.
Although rare, nodular fasciitis and solitary fibrous tumor arise in oral submucosa, usually in the cheek. The histopathologic features and immunomarkers indicative of myofibroblastic differentiation are seen in nodular fasciitis, whereas solitary fibrous tumor is CD34-positive; however, one instance was found to be positive for both markers. All of these cases harbored subpopulations of CD68-positive cells. Immunomarkers are a valuable adjunct in differentiating nodular fasciitis from solitary fibrous tumor, yet some tumors may harbor heterogeneous fibroblast phenotypes.
口腔内的纤维母细胞增生极为多样,但它们具有某些共同特征——梭形细胞形态、胶原蛋白合成以及束状排列。结节性筋膜炎是一种细胞性纤维母细胞病变,罕见于口腔黏膜下层,显示平滑肌肌动蛋白(SMA)免疫反应性。孤立性纤维瘤表达CD34纤维母细胞表型。本研究的目的是报告口面部区域结节性筋膜炎和孤立性纤维瘤的病例,并研究免疫组化标志物,以比较和对比这些肿瘤中纤维母细胞表型的异质性。
对10年间最初诊断为结节性筋膜炎的7例良性细胞性纤维生成性肿瘤进行检查。使用包括S-100蛋白、SMA、CD68、CD34和波形蛋白在内的免疫组化标志物对这些病变进行进一步特征分析。
所有肿瘤均发生于成年人,颊黏膜为好发部位。这些肿瘤中的梭形细胞在肿瘤内部以及不同肿瘤之间均表现出表型异质性。所有肿瘤均对波形蛋白呈反应性,并含有少量CD68阳性巨噬细胞/树突状细胞。5例肿瘤SMA阳性而CD34阴性;1例肿瘤SMA阴性而CD34阳性,另1例肿瘤SMA阳性且CD34阳性。
尽管罕见,但结节性筋膜炎和孤立性纤维瘤发生于口腔黏膜下层,通常在颊部。结节性筋膜炎可见提示肌纤维母细胞分化的组织病理学特征和免疫标志物,而孤立性纤维瘤CD34阳性;然而,发现1例肿瘤两种标志物均为阳性。所有这些病例均含有CD68阳性细胞亚群。免疫标志物在鉴别结节性筋膜炎和孤立性纤维瘤方面是有价值的辅助手段,但一些肿瘤可能具有异质性纤维母细胞表型。