首页> 外文期刊>International journal of gynecological pathology: Official journal of the International Society of Gynecological Pathologists >Differential vimentin expression in ovarian and uterine corpus endometrioid adenocarcinomas: Diagnostic utility in distinguishing double primaries from metastatic tumors
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Differential vimentin expression in ovarian and uterine corpus endometrioid adenocarcinomas: Diagnostic utility in distinguishing double primaries from metastatic tumors

机译:卵巢和子宫内膜样腺样腺癌中波形蛋白的差异表达:在区分双原发癌和转移性肿瘤中的诊断作用

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摘要

This study aimed to assess the diagnostic value of vimentin expression in differentiating endometrioid adenocarcinoma of primary uterine corpus and ovarian origin. Immunohistochemical analyses for the expression of vimentin in tumoral epithelial cells were performed on 149 endometrioid adenocarcinomas wherein the primary sites were not in question, including whole tissue sections of 27 carcinomas of uterine corpus origin (and no synchronous ovarian tumor), 7 carcinomas of ovarian origin (and no synchronous uterine corpus tumor) and a tissue microarray (TMA) containing 91 primary uterine corpus and 24 primary ovarian carcinomas. We also assessed 15 cases that synchronously involved the uterine corpus and ovary, 15 cases of metastasis to organs/tissues other than uterine corpus or ovary as well as 7 lymph node metastases. Vimentin was negative in 97% (30/31) of primary ovarian carcinomas. In contrast, 82% (97/118) of primary uterine corpus carcinomas were vimentin-positive. Vimentin expression was discordant in 53% of synchronous tumors. The sensitivity and specificity of negative vimentin staining in predicting an ovarian primary were 97% and 82%, respectively, whereas parallel values for positive vimentin staining in predicting a primary uterine tumor were 82% and 97%, respectively. The pattern of vimentin expression in all cases was maintained in their respective regional lymph nodes and distant metastases. In conclusion, ovarian and uterine corpus endometrioid adenocarcinomas have different patterns of vimentin expression. If validated in larger and/or different data sets, these findings may have diagnostic value in distinguishing metastatic lesions from double primary tumors involving both sites.
机译:本研究旨在评估波形蛋白表达在鉴别原发性子宫体和卵巢来源的子宫内膜样腺癌中的诊断价值。免疫组织化学分析了波形蛋白在肿瘤上皮细胞中的表达,涉及149个子宫内膜样腺癌,其中主要部位均无疑问,包括27例子宫体起源的癌的全组织切片(无同步卵巢肿瘤),7例卵巢起源的癌(并且没有同步子宫体肿瘤)和包含91个原发性子宫体和24个原发性卵巢癌的组织芯片(TMA)。我们还评估了15例同时涉及子宫体和卵巢的病例,15例转移至除子宫体或卵巢以外的器官/组织的病例以及7例淋巴结转移。波形蛋白在97%(30/31)的原发性卵巢癌中呈阴性。相反,82%(97/118)的原发性子宫体癌是波形蛋白阳性的。在53%的同步肿瘤中,波形蛋白的表达不一致。阴性波形蛋白染色在预测卵巢原发性中的敏感性和特异性分别为97%和82%,而阳性波形蛋白染色在预测原发性子宫肿瘤中的平行值分别为82%和97%。在所有情况下,波形蛋白的表达模式均维持在其各自的区域淋巴结和远处转移处。总之,卵巢和子宫体子宫内膜样腺癌具有波形蛋白表达的不同模式。如果在更大和/或不同的数据集中得到验证,这些发现可能对将转移性病变与涉及两个部位的双原发肿瘤区分开来具有诊断价值。

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