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Role of DNA flow cytometry and immunocytochemical analysis in diagnosis of malignant effusions

机译:DNA流式细胞仪和免疫细胞化学分析在恶性积液诊断中的作用

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摘要

Body cavity fluid examination sometimes presents a diagnostic challenge in cytology practice. This study was undertaken to evaluate efficacy of cytomorphology, epithelial membrane antigen immunocytochemistry (EMA-ICC) and DNA flow cytometry (FCM) in detection of malignant cells in effusions. One hundred effusions (55 pleural, 44 ascitic, and 1 pericardial fluid) were studied by cytology, EMA, and FCM. There were 29 malignant and 71 benign cases. On cytology, 28 of 29 malignant cases were diagnosed. With no false positives, the sensitivity and specificity was 96.55% and 100% respectively. FCM detected aneuploidy in 85.71% of cytologically malignant and 4.17% of cytologically benign effusions. EMA was positive in 75% of cytologically malignant and 4.17% of cytologically benign cases. EMA had lower sensitivity than cytology; 75.86% versus 96.55%. Sensitivity and specificity of FCM was 86.21%, and 97.18% respectively. FCM had lower sensitivity than cytology; 86.21% versus 96.55%. Sensitivity increased to 100% (P < 0.05) when the combinations of cytology plus EMA or cytology plus ploidy were applied compared to cytology alone (96.55%). Also, the combination of cytology plus EMA had higher sensitivity than EMA alone (100% versus 75.86%, P < 0.05) and combined cytology plus ploidy had higher sensitivity than ploidy alone (100% versus 86.21%, P < 0.05). The study demonstrates the usefulness of EMA-ICC and DNA FCM as adjuncts to cytology to diagnose malignancy in effusions. FCM in combination with ICC can be further developed to reduce number of false-negative cases on cytology and add objectivity to cytologically doubtful or equivocal cases. Diagn. Cytopathol. 2012.
机译:体液检查有时在细胞学实践中提出诊断挑战。这项研究旨在评估细胞形态学,上皮膜抗原免疫细胞化学(EMA-ICC)和DNA流式细胞仪(FCM)在检测积液中恶性细胞方面的功效。通过细胞学,EMA和FCM研究了一百次积液(55例胸水,44例腹水和1例心包积液)。有恶性29例,良性71例。细胞学诊断为29例恶性肿瘤中的28例。没有假阳性,敏感性和特异性分别为96.55%和100%。 FCM在85.71%的细胞恶性和4.17%的细胞良性积液中检测到非整倍性。 EMA在细胞学恶性肿瘤中占75%,在细胞学良性病例中占4.17%。 EMA的敏感性低于细胞学。 75.86%和96.55%。 FCM的敏感性和特异性分别为86.21%和97.18%。 FCM的敏感性低于细胞学。 86.21%和96.55%。与仅使用细胞学检查时(96.55%)相比,应用细胞学检查+ EMA或细胞学检查+倍性的组合时,灵敏度提高到100%(P <0.05)。另外,细胞学加EMA联合检测的敏感性高于单独的EMA(100%比75.86%,P <0.05),细胞学加倍性联合检测的敏感性高于单独的EMA(100%比86.21%,P <0.05)。这项研究证明了EMA-ICC和DNA FCM作为细胞学检查的辅助手段可用于诊断积液中的恶性肿瘤。 FCM与ICC的结合可以进一步发展,以减少细胞学上假阴性病例的数量,并为细胞学上可疑或模棱两可的病例增加客观性。诊断细胞病。 2012。

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