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Diagnostic value of clot examination for malignant cells in serous effusions

机译:凝块检查对浆液性恶性细胞的诊断价值

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Objective: To assess the diagnostic value of clot examination for satisfactory processing and confirmation of malignancy in serous effusions in routine cytological evaluation and compare the results with those of conventional smear and cell block preparations. Methodology: Body cavity fluids (n = 600) received in our laboratory were processed according to a pre-designed protocol for the study as follows: Day1: on receipt of the specimen, smears were made and a cell block was prepared from the sediment. Day2: after overnight sample storage of the remaining specimen at 2-8 °C all fluids were examined for the presence of a clot at the bottom of the container. Fluids in which clot had formed were fixed in formalin. The clot was then placed on a lens paper, wrapped and processed routinely. Diagnostic yields were compared. Results: In this study, we included 600 cases of serous fluids from pleural, pericardial and peritoneal effusions. In 73% (n = 437) of samples, clot formation was seen, while in 27%, (n = 163) no clot had formed. Routine smear and cell block preparations showed malignant cells in 9.6% (n = 42). However, with the addition of the clot preparation, the number of cases in which atypical/malignant cells were seen increased from 42 to 85 (19.4%), with a P < 0.001. Special stains and immunohistochemistry (IHC) were also performed on clot preparations in 10 difficult cases. Conclusion: Clot preparation from body cavity fluids on the second day can be used as an adjunct to smear and routine cell block preparation to improve the accuracy and yield of the cytological diagnosis and may also be of great help for special studies such as IHC staining.
机译:目的:在常规细胞学评估中评估凝块检查对浆液性积液的满意处理和恶性确认的诊断价值,并将其结果与常规涂片和细胞块制剂的结果进行比较。方法:按照预先设计的研究方案,对在我们实验室中接受的体腔积液(n = 600)进行如下处理:第1天:在收到标本后,进行涂片检查,并从沉积物中制备细胞块。第2天:在2-8°C下过夜保存剩余样品的样品后,检查所有液体在容器底部是否存在凝块。将形成凝块的液体固定在福尔马林中。然后将血块放在镜纸上,进行常规包装和处理。比较诊断结果。结果:在这项研究中,我们纳入了600例胸膜,心包和腹膜积液的浆液。在73%(n = 437)的样本中,发现有血块形成,而在27%(n = 163)的样本中,没有形成血块。常规涂片和细胞块制剂显示恶性细胞占9.6%(n = 42)。但是,添加凝块制剂后,发现非典型/恶性细胞的病例数从42增加到85(19.4%),P <0.001。在10个困难病例中,还对凝块制备物进行了特殊染色和免疫组化(IHC)。结论:第二天从体腔积液准备的血块可作为涂片和常规细胞块制备的辅助手段,以提高细胞学诊断的准确性和产率,也可能对IHC染色等特殊研究大有帮助。

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