Kanitakis J, Bendelac A, Marchand C, Rigot-Muller G, Thivolet J
J Cutan Pathol. 1986 Feb;13(1):30-9. doi: 10.1111/j.1600-0560.1986.tb00458.x.
One case of the so-called "Stewart-Treves syndrome" (STS), appearing on a lymphoedematous arm complicating radical mastectomy for breast cancer, was characterized electronmicroscopically and immunohistologically, in order to elucidate its disputed (epithelial vs endothelial) histogenesis. Epithelial and endothelial differentiation markers used comprised: antibodies against keratin, vimentin, factor VIII-related antigen (F VIII-RA), HLA-DR antigens and the lectin Ulex europeaus agglutinin I (UEA I). At the ultrastructural level, neoplastic cells were found to contain typical Weibel-Palade bodies, whereas by immunohistological techniques they proved to be keratin-negative/vimentin+, F VIII-RA+, UEAI+, HLA-DR+. These results rule out a possible epithelial differentiation and strongly favour an endothelial one for STS.
对1例发生于乳腺癌根治术后并发淋巴水肿上肢的所谓“斯图尔特-特里夫斯综合征”(STS)进行了电镜和免疫组织学特征分析,以阐明其存在争议的(上皮性与内皮性)组织发生。所使用的上皮和内皮分化标志物包括:抗角蛋白、波形蛋白、因子VIII相关抗原(F VIII-RA)、HLA-DR抗原的抗体以及凝集素欧洲荆豆凝集素I(UEA I)。在超微结构水平上,发现肿瘤细胞含有典型的魏贝尔-帕拉德小体,而通过免疫组织学技术证实它们角蛋白阴性/波形蛋白阳性、F VIII-RA阳性、UEA I阳性、HLA-DR阳性。这些结果排除了STS可能的上皮分化,强烈支持其内皮分化。