Dardick I, Van Nostrand A W, Jeans M T, Rippstein P, Edwards V
Hum Pathol. 1983 Sep;14(9):798-809. doi: 10.1016/s0046-8177(83)80302-5.
Findings from an ultrastructural study of 24 major and minor salivary gland pleomorphic adenomas suggest that the principal cell type in the myxoid and chondromyxoid regions of these tumors is a structurally modified myoepithelial cell. This interpretation is based on findings in the transitional zone between myxoid regions and compact cellular areas that have a ductal-acinar organization, that is, are composed of luminal epithelial and modified myoepithelial cells. Survey-type low-power electron micrographs allowed appreciation of the original orientation of the major proliferating component of these tumors to the perimeter of ductal-acinar units. The low-power electron micrographs also revealed residual features of this organization, the early development and subsequent sequential alteration of matrix compartments as tumor cells became increasingly separated by extracellular products, and a variety of myoepithelial cell modifications, such as squamous and chondroid metaplasia, resulting from neoplastic induction. According to the authors' interpretation, modified myoepithelial cells in myxoid and chondromyxoid regions form a continuum with similar tumor cells in transitional and solid areas, forming what can be visualized as markedly expanded and merging ductal-acinar units that tend to converge with similarly altered adjacent neoplastic ductal-acinar units. Thus, a multiplicity of processes are involved in the formation of the complex and varied histologic patterns that characterize pleomorphic adenomas.
一项对24例大、小涎腺多形性腺瘤的超微结构研究结果表明,这些肿瘤黏液样和软骨黏液样区域的主要细胞类型是结构改变的肌上皮细胞。这一解释基于在黏液样区域和具有导管-腺泡组织结构(即由管腔上皮细胞和改良肌上皮细胞组成)的致密细胞区域之间的过渡区的研究发现。概观型低倍电子显微镜图像使人们能够了解这些肿瘤主要增殖成分相对于导管-腺泡单位周边的原始取向。低倍电子显微镜图像还揭示了这种组织结构的残余特征、随着肿瘤细胞被细胞外产物逐渐分隔而导致的基质隔室的早期发育和随后的顺序改变,以及由肿瘤诱导导致的多种肌上皮细胞改变,如鳞状化生和软骨样化生。根据作者的解释,黏液样和软骨黏液样区域的改良肌上皮细胞与过渡区和实性区域的类似肿瘤细胞形成连续体,形成可被视为明显扩张和融合的导管-腺泡单位,这些单位倾向于与相邻的、同样改变的肿瘤性导管-腺泡单位汇聚。因此,多种过程参与了构成多形性腺瘤特征的复杂多样的组织学模式的形成。