Stege R, Lundh B, Tribukait B, Pousette A, Carlström K, Hasenson M
Department of Urology, Karolinska Institutet, Huddinge University Hospital, Sweden.
J Urol. 1990 Aug;144(2 Pt 1):299-302. doi: 10.1016/s0022-5347(17)39436-3.
We used fine needle biopsies from prostatic tumors at routine examinations in 133 patients. Cytological grading was performed with a scoring system. Cellular prostatic acid phosphatase and cellular prostate specific antigen from the aspirates were quantitated. Deoxyribonucleic acid flow cytometry was performed and the tumors were subdivided into diploid, tetraploid and aneuploid groups. Tumor staging was assessed by digital examination. A decrease in the biochemical markers was significantly correlated with the increase in malignancy grade, tumor stage and a shift from diploid to aneuploid tumors. Cellular prostatic acid phosphatase and cellular prostate specific antigen as well as tumor ploidy may contribute to the objective determination of the malignancy potential of the prostatic carcinoma.
我们在133例患者的常规检查中采用前列腺肿瘤细针穿刺活检。采用评分系统进行细胞学分级。对穿刺液中的细胞前列腺酸性磷酸酶和细胞前列腺特异性抗原进行定量分析。进行脱氧核糖核酸流式细胞术检测,并将肿瘤分为二倍体、四倍体和非整倍体组。通过直肠指诊评估肿瘤分期。生化标志物的降低与恶性程度分级增加、肿瘤分期以及从二倍体肿瘤向非整倍体肿瘤的转变显著相关。细胞前列腺酸性磷酸酶、细胞前列腺特异性抗原以及肿瘤倍性可能有助于客观判定前列腺癌的恶性潜能。