Eckert F, Nilles M, Altmannsberger M
Department of Dermatology, University of Munich, Germany.
Br J Dermatol. 1992 Mar;126(3):257-61. doi: 10.1111/j.1365-2133.1992.tb00655.x.
A 56-year-old man presented with a 30-year history of a slowly enlarging lesion on the sole of his right foot. A biopsy showed an anastomosing network of small cuboidal cells with the formation of occasional sweat ductal lumina and a marked fibrovascular stroma. The histological findings were interpreted as consistent with the diagnosis of an eccrine syringofibroadenoma. Using immunohistochemistry all the tumour cells were positively stained by the pan-cytokeratin antibody Lu-5 and an antibody to the cytokeratins 1/5/10/11. In addition the luminal ductal cells expressed cytokeratin 19 and CEA. Tumour cells were negative for cytokeratins 1, 7, 8, 13 and 18 and did not express vimentin and GCDFP-15. The results indicate that the eccrine syringofibroadenoma is differentiated towards the dermal eccrine duct.
一名56岁男性,其右脚脚底有一缓慢增大的肿物,病史长达30年。活检显示由小立方形细胞构成的吻合网络,偶见汗腺导管腔形成,并有明显的纤维血管间质。组织学表现被解释为符合小汗腺汗管纤维腺瘤的诊断。采用免疫组织化学方法,所有肿瘤细胞均被泛细胞角蛋白抗体Lu-5和细胞角蛋白1/5/10/11抗体阳性染色。此外,管腔导管细胞表达细胞角蛋白19和癌胚抗原。肿瘤细胞细胞角蛋白1、7、8、13和18呈阴性,不表达波形蛋白和GCDFP-15。结果表明,小汗腺汗管纤维腺瘤向真皮小汗腺导管分化。