Mezger J, Permanetter W, Gerbes A L, Wilmanns W, Lamerz R
Department of Medicine III, Klinikum Grosshadern, University of Munich, West Germany.
J Clin Pathol. 1988 Jun;41(6):633-43. doi: 10.1136/jcp.41.6.633.
The use of tumour associated antigens in the diagnosis of serous effusions was studied in 76 patients with benign and 200 patients with malignant disease. Tissue polypeptide antigen (TPA), alpha fetoprotein, and CA 125 were found to be of little value. At cut off points of 3 ng/ml, 10 U/ml, and 30 U/ml, respectively, carcinoembryonic antigen (CEA), biliary glycoprotein I (BGP I), and CA 19-9 discriminated between benign and malignant serous effusions with a sensitivity of between 24% and 67%. The immunocytochemical staining for these markers resulted in malignant cells being detected in 18% to 33% of cases. Various combinations of conventional cytological examination, effusion fluid tumour marker determination, and immunocytochemical analysis identified malignant cells in serous effusions in up to 72% of cases; conventional cytology alone detected tumour cells in only 30%.
对76例良性疾病患者和200例恶性疾病患者进行了肿瘤相关抗原在浆液性积液诊断中的应用研究。发现组织多肽抗原(TPA)、甲胎蛋白和CA 125价值不大。癌胚抗原(CEA)、胆汁糖蛋白I(BGP I)和CA 19-9分别在3 ng/ml、10 U/ml和30 U/ml的临界值时,区分良性和恶性浆液性积液的敏感性在24%至67%之间。这些标志物的免疫细胞化学染色在18%至33%的病例中检测到恶性细胞。传统细胞学检查、积液肿瘤标志物测定和免疫细胞化学分析的各种组合在高达72%的病例中识别出浆液性积液中的恶性细胞;仅传统细胞学检查仅在30%的病例中检测到肿瘤细胞。