免疫组化标记物SATB2和绒毛蛋白在卵巢和胃肠道黏液癌鉴别诊断中的准确性评价。

IF 1.2
Mehrjoo Amraie, Mohammadhossein Khorraminejad-Shirazi, Ali Nabavizadeh, Maral Mokhtari
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引用次数: 0

摘要

由于组织学和免疫组织化学特征重叠,确定粘液腺癌的起源可能具有挑战性。本研究评估了SATB2和绒毛蛋白免疫组织化学标记物在确定粘液腺癌起源方面的效用。我们回顾性分析了71例粘液腺癌患者——31例下胃肠道(GI), 28例卵巢,12例腹膜假性粘液瘤。对卵巢和胃肠道肿瘤进行SATB2和绒毛蛋白的免疫组化。计算敏感性、特异性、阳性和阴性预测值来评估诊断性能。SATB2的敏感性为87.1%,特异度为100%;villin的敏感性为93.5%,特异度仅为21.4%。SATB2/villin双阳性对胃肠道来源的敏感性为80.6%,特异性为100%。对于卵巢来源,SATB2/villin双阴性提供100%的特异性。对腺癌病例进行Logistic回归分析,SATB2和绒毛蛋白双染色预测胃肠道与卵巢起源的准确率为93.2%。SATB2对胃肠道粘液腺癌具有高特异性,而绒毛蛋白对胃肠道粘液腺癌具有高敏感性。结合SATB2和绒毛蛋白可优化鉴别粘液腺癌原发部位和确定腹膜假性黏液瘤起源的诊断性能。此外,在我们的病例中,印戒形态的存在促使我们重新考虑可能的GI起源。包括SATB2和绒毛蛋白在内的多标记免疫组化检测可提高挑战性粘液腺癌病例的诊断准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Diagnostic Accuracy of Immunohistochemical Markers of SATB2 and Villin in Differential Diagnosis of Ovarian and Gastrointestinal Mucinous Carcinoma.

Determining the origin of mucinous adenocarcinomas can be challenging due to overlapping histologic and immunohistochemical features. This study evaluates the utility of SATB2 and villin immunohistochemical markers for defining mucinous adenocarcinomas' origin. We retrospectively analyzed 71 patients with mucinous adenocarcinomas-31 lower gastrointestinal (GI), 28 ovarian, and 12 cases of pseudomyxoma peritonei. Immunohistochemistry for SATB2 and villin was performed on ovarian and GI tumor samples. Sensitivity, specificity, and positive and negative predictive values were calculated to assess diagnostic performance.For identifying GI origin, SATB2 showed 87.1% sensitivity and 100% specificity, while villin exhibited 93.5% sensitivity but only 21.4% specificity. Dual SATB2/villin positivity demonstrated 80.6% sensitivity and 100% specificity for GI origin. For ovarian origin, dual SATB2/villin negativity provided 100% specificity. Logistic regression analysis on the adenocarcinoma cases showed 93.2% accuracy rate of dual staining with SATB2 and villin for predicting GI versus ovarian origin. SATB2 exhibits high specificity for GI mucinous adenocarcinomas, and villin is highly sensitive. Combining SATB2 and villin optimizes diagnostic performance for differentiating the primary origin site of mucinous adenocarcinomas and determining pseudomyxoma peritonei origin. Moreover, the presence of signet ring morphology prompted reconsideration of possible GI origin among our cases. A multimarker immunohistochemical panel, including SATB2 and villin can enhance the diagnostic accuracy of challenging mucinous adenocarcinoma cases.

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