Goddard M J, Grant J W
Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.
Histopathology. 1992 Jan;20(1):57-61. doi: 10.1111/j.1365-2559.1992.tb00917.x.
We have examined 16 cases of adenomatoid tumour using a panel of monoclonal and polyclonal antibodies and also stained them for the presence of hyaluronidase-sensitive alcianophilic material. Fourteen cases expressed cytokeratins and a proportion of these also expressed S-100 protein, neuron-specific enolase, vimentin, and human milk fat globule protein 2. The same 14 cases also showed hyaluronidase-sensitive staining with alcian blue. No expression of factor VIII-related antigen was seen in these cases. We conclude that this provides further evidence of a mesothelial origin of these tumours. The remaining two cases did not express cytokeratins and no hyaluronidase-sensitive staining with alcian blue was seen. They did however express factor VIII-related antigen. Although they were morphologically indistinguishable from the other 14 cases, we suggest that they should be more properly regarded as angiomas.
我们使用一组单克隆和多克隆抗体检查了16例腺瘤样瘤病例,并对其进行染色以检测透明质酸酶敏感的嗜碱性物质的存在。14例病例表达细胞角蛋白,其中一部分还表达S-100蛋白、神经元特异性烯醇化酶、波形蛋白和人乳脂肪球蛋白2。同样的14例病例也显示对阿尔辛蓝呈透明质酸酶敏感染色。这些病例中未见到因子VIII相关抗原的表达。我们得出结论,这为这些肿瘤的间皮起源提供了进一步的证据。其余2例病例不表达细胞角蛋白,未见到对阿尔辛蓝的透明质酸酶敏感染色。然而,它们表达因子VIII相关抗原。尽管它们在形态上与其他14例病例无法区分,但我们认为它们更应被视为血管瘤。