Labonté S, Têtu B, Boucher D, Larue H
Department of Pathology, Centre Hospitalier Universitaire de Québec, Laval University, Québec, Canada.
Hum Pathol. 2001 Feb;32(2):230-2. doi: 10.1053/hupa.2001.20900.
Transitional cell carcinomas (TCCs) of the endometrium are rare, and only 10 cases have been described to date. We report the case of a 46-year-old woman who developed both a TCC of the endometrium and a benign ovarian Brenner tumor. Such an association has not yet been reported in the literature. Immunohistochemical studies of the uterine tumor showed cytokeratin 7 positivity and cytokeratin 20 negative staining, which was consistent with a Müllerian derivation. Human papilloma virus (HPV) immunostaining as well as polymerase chain reaction (PCR) analysis using primers for HPV types 6, 11, 16, and 18 failed to detect viral DNA. The coexistence of a TCC of the endometrium and an ovarian Brenner tumor might be coincidental but raises the possibility of a field effect, as seen with multifocal endometrioid tumors or multiple urinary tract TCCs.
子宫内膜移行细胞癌(TCC)较为罕见,迄今为止仅有10例相关病例报道。我们报告了一例46岁女性,其同时患有子宫内膜TCC和良性卵巢布伦纳瘤。这种关联在文献中尚未见报道。对子宫肿瘤进行的免疫组织化学研究显示细胞角蛋白7呈阳性,细胞角蛋白20呈阴性染色,这与苗勒氏来源一致。人乳头瘤病毒(HPV)免疫染色以及使用针对HPV 6、11、16和18型的引物进行的聚合酶链反应(PCR)分析均未检测到病毒DNA。子宫内膜TCC与卵巢布伦纳瘤的共存可能是巧合,但也增加了出现如多灶性子宫内膜样肿瘤或多发性泌尿道TCC所见的场效应的可能性。