Herrera G A, Reimann B E, Salinas J A, Turbat E A
Ultrastruct Pathol. 1982 Jul-Sep;3(3):253-61. doi: 10.3109/01913128209016651.
Two soft tissue neoplasms considered to represent malignant fibrous histiocytomas by light microscopy showed typical findings indicative of Schwann cell origin when examined by electron microscopy. These findings included the presence of cells exhibiting long interdigitating cytoplasmic processes, which frequently contained collections of microtubules and were surrounded by thin, frequently interrupted, basal lamina material. In addition, pinocytotic activity at the cell surfaces and immature junctions joining apposing cellular membranes were identified. No evidence of fibroblastic, fibrohistiocytic, or myofibroblastic differentiation was identified ultrastructurally in the neoplastic cells. Our findings stress the need for ultrastructural examination to adequately classify soft tissue sarcomas. The 2 cases presented illustrate that there are some schwannomas that may be inaccurately classified as malignant fibrous histiocytomas if only light microscopy is used. It seems that only by ultrastructural means is it possible to accurately classify these peculiar neoplasms.
两个在光学显微镜下被认为是恶性纤维组织细胞瘤的软组织肿瘤,在进行电子显微镜检查时显示出典型的提示施万细胞起源的特征。这些特征包括存在具有长的相互交错的细胞质突起的细胞,这些突起经常含有微管集合,并被薄的、经常中断的基底膜物质包围。此外,在细胞表面鉴定出吞饮活性以及连接相对细胞膜的不成熟连接。在肿瘤细胞的超微结构中未发现成纤维细胞、纤维组织细胞或肌成纤维细胞分化的证据。我们的发现强调了超微结构检查对于充分分类软组织肉瘤的必要性。所呈现的这2例病例表明,如果仅使用光学显微镜,一些施万瘤可能会被不准确地分类为恶性纤维组织细胞瘤。似乎只有通过超微结构手段才有可能准确分类这些特殊的肿瘤。