Eyden B, Banerjee S S, Shenjere P, Fisher C
Department of Histopathology, Christie Hospital NHS Foundation Trust, Manchester, UK.
J Clin Pathol. 2009 Mar;62(3):236-49. doi: 10.1136/jcp.2008.061630. Epub 2008 Oct 17.
Tumours and tumour-like lesions of myofibroblasts may present diagnostic difficulty because of their rarity and because of uncertainties in identifying the myofibroblast. The objectives of this review are to provide a definition of the myofibroblast and an account of its biology for facilitating an understanding of the cell and of myofibroblastic lesions; and to describe, in the context of common diagnostic problems, the features of benign and malignant myofibroblastic lesions. The main characteristics of the myofibroblast include a spindled or stellate morphology; immunostaining for alpha-smooth muscle actin and the extra domain A variant of cellular fibronectin; and an ultrastructure of rough endoplasmic reticulum, peripheral contractile filaments and the cell-to-matrix junction known as the fibronexus. On this basis, lesions traditionally regarded as myofibroblastic are shown to vary in their level of differentiation, and some appear to be smooth muscle rather than myofibroblastic. Immunohistochemistry and electron microscopy, used together, are emphasised as being important for maximum diagnostic confidence in some myofibroblastic lesions.
肌成纤维细胞的肿瘤及肿瘤样病变可能会带来诊断困难,这是因为它们较为罕见,且在识别肌成纤维细胞方面存在不确定性。本综述的目的是给出肌成纤维细胞的定义并阐述其生物学特性,以助于理解该细胞及肌成纤维细胞性病变;并在常见诊断问题的背景下,描述良性和恶性肌成纤维细胞性病变的特征。肌成纤维细胞的主要特征包括梭形或星状形态;α平滑肌肌动蛋白和细胞纤连蛋白额外结构域A变体的免疫染色;以及具有粗面内质网、周边收缩丝和称为纤维连接的细胞与基质连接的超微结构。在此基础上,传统上被视为肌成纤维细胞性的病变在其分化程度上存在差异,有些似乎是平滑肌而非肌成纤维细胞性的。强调免疫组织化学和电子显微镜联合使用对于某些肌成纤维细胞性病变获得最大诊断信心很重要。