Immunohistochemical evidence for mesothelial origin of paratesticular adenomatoid tumour

被引:1
作者
Delahunt, B
Eble, JN
King, D
Bethwaite, PB
Nacey, JN
Thornton, A
机构
[1] Univ Otago, Wellington Sch Med, Dept Pathol, Wellington, New Zealand
[2] Univ Otago, Wellington Sch Med, Dept Surg, Wellington, New Zealand
[3] Indiana Univ, Dept Pathol & Lab Med, Indianapolis, IN 46204 USA
关键词
adenomatoid tumour; immunohistochemistry; mesothelial cell; mesothelioma; pathogenesis;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To investigate the histogenesis of paratesticular adenomatoid tumour by use of immunohistochemical markers for a variety of carcinomas and mesothelioma, Methods and results: Immunohistochemical staining of sections from 12 cases of paratesticular adenomatoid tumour was undertaken using primary antibodies to antigens expressed by benign epithelial cells and carcinoma (cytokeratin AE1/AE3, cytokeratin 34BE312, epithelial membrane antigen, MOC-31, Ber-EP4, CEA, B72.3, LEA.135, Leu Mi), stromal and vascular markers (vimentin, CD34, factor VIII), and mesothelioma-associated antigens (thrombomodulin, HBME-1, OC 125) and p53 protein. There was absence of immunohistochemical expression of epithelial/ carcinoma markers MOC-31, Ber-EP4, CEA, B72.3, LEA.135, Leu M1 and to factor VIII and CD34. All tumours expressed cytokeratin AE1/AE3, epithelial membrane antigen and vimentin, with weak expression of cytokeratin 34BE12 in 25% of tumours. Each tumour showed expression of thrombomodulin, HBME-1 and OC 125 in a membranous distribution, p53 protein expression was not detected. Conclusions: The immunohistochemical profile of paratesticular adenomatoid tumour is strongly supportive of a mesothelial cell origin.
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页码:109 / 115
页数:7
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