Arber D A, Kandalaft P L, Mehta P, Battifora H
Division of Pathology, City of Hope National Medical Center, Duarte, California 91010.
Am J Surg Pathol. 1993 Mar;17(3):302-7.
Virtually all reported cases of epithelioid sarcoma have been vimentin rich, and the coexpression of vimentin and keratin is considered a characteristic immunophenotype in these tumors. We report three cases of soft tissue tumors with histologic and clinical features consistent with epithelioid sarcoma, all of which failed to immunoreact by standard immunohistochemistry for vimentin using two different monoclonal antibodies. Antigen retrieval demonstrated focal vimentin staining in one case, whereas the other two remained negative. An extensive panel of immunohistochemical stains revealed strong diffuse staining with keratin and epithelial membrane antigen in all three cases as well as patchy membrane staining with an antibody to CD34. CD34 positivity is commonly seen in epithelioid sarcoma, but it is very rarely found in carcinomas. We conclude that these cases represent a unique immunophenotypic variant of epithelioid sarcoma that can be immunohistochemically confirmed, despite the lack of identifiable vimentin, by their immunoreactivity for keratin and CD34.
几乎所有已报道的上皮样肉瘤病例都富含波形蛋白,波形蛋白和角蛋白的共表达被认为是这些肿瘤的特征性免疫表型。我们报告了三例软组织肿瘤,其组织学和临床特征与上皮样肉瘤一致,所有这些病例使用两种不同的单克隆抗体进行标准免疫组织化学检测波形蛋白时均未出现免疫反应。抗原修复显示其中一例有局灶性波形蛋白染色,而另外两例仍为阴性。一系列广泛的免疫组织化学染色显示,所有三例病例中角蛋白和上皮膜抗原均呈强弥漫性染色,以及用抗CD34抗体进行的斑片状膜染色。CD34阳性在上皮样肉瘤中常见,但在癌中很少见。我们得出结论,这些病例代表了上皮样肉瘤的一种独特免疫表型变异,尽管缺乏可识别的波形蛋白,但通过其对角蛋白和CD34的免疫反应性可通过免疫组织化学得到证实。