Hanai J, Lin M
Department of Pathology, Sakai Municipal Hospital, Osaka, Japan.
Acta Pathol Jpn. 1990 Nov;40(11):838-44. doi: 10.1111/j.1440-1827.1990.tb02498.x.
A rare case of adenocarcinoma of the female urethra with alpha-fetoprotein (AFP) positivity in a 52-year-old woman is reported. The tumor was papillary polypoid, localized in the posterior wall of the mid-urethra and microscopically showed three histologic components. Upon immunostaining and histochemical staining, the tumor was characterized by intestinal-type cells positive for epithelial membrane antigen (EMA) and carcinoembryonic antigen (CEA), EMA-negative and AFP-positive columnar vacuolated cells and mainly EMA-positive clear cells. On the basis of these features together with the known embryogenesis of the urethra, an endodermal origin of the tumor is suggested, possibly arising from the reserve or stem cells in the urethral mucosa. This case and its immunohistochemical features are quite unique and the histologic combination is meaningful when considering the oncogenesis and histogenesis of urethral tumors.
报告了一例52岁女性罕见的女性尿道腺癌,该肿瘤甲胎蛋白(AFP)呈阳性。肿瘤为乳头状息肉样,位于尿道中段后壁,显微镜下显示三种组织学成分。经免疫染色和组织化学染色,肿瘤特征为上皮膜抗原(EMA)和癌胚抗原(CEA)阳性的肠型细胞、EMA阴性且AFP阳性的柱状空泡细胞以及主要为EMA阳性的透明细胞。基于这些特征以及已知的尿道胚胎发生过程,提示肿瘤起源于内胚层,可能源自尿道黏膜中的储备细胞或干细胞。该病例及其免疫组化特征非常独特,这种组织学组合在考虑尿道肿瘤的肿瘤发生和组织发生时具有重要意义。