Dardick I, Cavell S, Boivin M, Hoppe D, Parks W R, Stinson J, Yamada S, Burns B F
Department of Pathology, University of Toronto, Banting Institute, Ontario, Canada.
Virchows Arch A Pathol Anat Histopathol. 1989;416(1):25-42. doi: 10.1007/BF01606467.
The histological and ultrastructural features of five major salivary gland tumours, which have little or no evidence of duct- or gland-type differentiation in routine sections, are described. Four of the cases have the tumour cells organized as narrow, anastomosing cords of cells separated by a myxoid and vascularized stroma; we have designated such lesions as reticular-type myoepitheliomas. The fifth case has a solid growth pattern and is largely composed of hyaline cells, that is, a plasmacytoid myoepithelioma. Ultrastructurally, one reticular myoepithelioma reveals myoepithelial cell differentiation with microfilament aggregates, while the other three examples are composed of modified myoepithelial cells displaying widened intercellular spaces, prominent synthesis of extracellular glycosaminoglycans, distinct basal lamina development, and obvious accumulations of cytoplasmic intermediate filaments. In electron micrographs, the modified myoepithelial cells of the plasmacytoid variant closely resemble the tumour cells in the reticular form. Three cases had expression of both glial fibrillary acid protein (GFAP) and vimentin, but only one of the myoepitheliomas contained muscle-specific actin. At least focally, each of the cases exhibited a considerable spectrum of cytokeratin filaments. Using double-labeled immunofluorescent microscopy of one reticular variant and the plasmacytoid myoepithelioma, there was individual tumour cell co-expression of GFAP and vimentin focally in the plasmacytoid myoepithelioma, but co-expression of cytokeratins 13, 16 and GFAP were not noted in either case. As expected, co-expression of high- and low-molecular weight cytokeratin filaments was widespread in both myoepitheliomas. Most described myoepitheliomas have a solid growth pattern and are composed of spindle and plasmacytoid cells, but based on cytological features and growth patterns in this series, it is apparent that polygonal-shaped cells with novel architecture can occur in myoepitheliomas. The results also indicate the close relationship between pleomorphic adenoma and such variants of myoepithelioma.
本文描述了五种主要唾液腺肿瘤的组织学和超微结构特征,这些肿瘤在常规切片中几乎没有或没有导管或腺型分化的证据。其中四例病例的肿瘤细胞组织成狭窄的、相互吻合的细胞索,由黏液样和血管化的间质分隔;我们将此类病变命名为网状型肌上皮瘤。第五例病例具有实性生长模式,主要由透明细胞组成,即浆细胞样肌上皮瘤。超微结构上,一例网状肌上皮瘤显示肌上皮细胞分化,有微丝聚集,而其他三例由改良的肌上皮细胞组成,这些细胞显示细胞间隙增宽、细胞外糖胺聚糖合成显著、基底膜发育明显以及细胞质中间丝明显聚集。在电子显微镜照片中,浆细胞样变体的改良肌上皮细胞与网状形式的肿瘤细胞非常相似。三例病例同时表达胶质纤维酸性蛋白(GFAP)和波形蛋白,但只有一例肌上皮瘤含有肌肉特异性肌动蛋白。至少在局部,每例病例都表现出相当广泛的细胞角蛋白丝谱。使用一例网状变体和浆细胞样肌上皮瘤的双标记免疫荧光显微镜检查,浆细胞样肌上皮瘤中个别肿瘤细胞局部共表达GFAP和波形蛋白,但在这两种情况下均未观察到细胞角蛋白13、16和GFAP的共表达。正如预期的那样,高分子量和低分子量细胞角蛋白丝的共表达在两种肌上皮瘤中都很普遍。大多数已描述的肌上皮瘤具有实性生长模式,由梭形和浆细胞样细胞组成,但基于本系列中的细胞学特征和生长模式,很明显肌上皮瘤中可以出现具有新结构的多边形细胞。结果还表明多形性腺瘤与这种肌上皮瘤变体之间存在密切关系。