Auböck L
Virchows Arch A Pathol Anat Histol. 1975 Oct 30;368(3):253-74. doi: 10.1007/BF00432527.
A report on the ultrastructure of the following skin tumors: dermatofibroma (7 cases), histiocytoma (4 cases), dermatofibrosarcoma protuberans (1 case), and fibroxanthoma (1 case). Because of their different ultrastructural characteristics a division into two groups is possible: one group of tumors would include dermatofibroma, dermatofibrosarcoma protuberans, and fibroxanthoma, where the formation of fibers is extensive and fibroblasts are suggested for its histogenesis. These types of tumor differ from histiocytoma, the cellular character of which is determined by a very pronounced phagocytosis and storage of lipid and hemosiderin; a histogenesis from histiocytes is probable. The nuclei of dermatofibroma and histiocytoma show a simple surfacedevelopment, whereas the nuclei of dermatofibrosarcoma protuberans and fibroxanthoma show multisegmented nuclei ("labyrinth nuclei"). In the case of dermatofibrosarcoma protuberans this kind of nuclear segmentation seems to be a morphologic correlate of its semimalignancy. Based on ultrastructural analysis a classification of these fiber-producing tumors into "fibrous histiocytomas" is not justified.
皮肤纤维瘤(7例)、组织细胞瘤(4例)、隆突性皮肤纤维肉瘤(1例)和纤维黄色瘤(1例)。由于它们不同的超微结构特征,可分为两组:一组肿瘤包括皮肤纤维瘤、隆突性皮肤纤维肉瘤和纤维黄色瘤,这些肿瘤中纤维形成广泛,其组织发生提示为成纤维细胞。这些肿瘤类型与组织细胞瘤不同,组织细胞瘤的细胞特征由非常明显的脂质和含铁血黄素吞噬及储存所决定;可能起源于组织细胞。皮肤纤维瘤和组织细胞瘤的细胞核表现为简单的表面发育,而隆突性皮肤纤维肉瘤和纤维黄色瘤的细胞核表现为多节段核(“迷宫核”)。在隆突性皮肤纤维肉瘤中,这种核分割似乎是其半恶性的形态学相关表现。基于超微结构分析,将这些纤维生成性肿瘤归类为“纤维组织细胞瘤”是不合理的。