首页 | 本学科首页   官方微博 | 高级检索  
检索        

f/tPSA比值在前列腺增生与前列腺癌的诊断价值
引用本文:许绍国,朱联生.f/tPSA比值在前列腺增生与前列腺癌的诊断价值[J].安徽卫生职业技术学院学报,2011,10(5):84-85.
作者姓名:许绍国  朱联生
作者单位:合肥市第三人民医院 安徽232000
摘    要:目的:探讨血清中的前列腺特异性抗原(tPSA)、游离PSA(fPSA)及f/tPSA对前列腺增生(BHP)与前列腺癌(PCA)的诊断价值。方法:采用免疫荧光法检测经病理诊断60例前列腺增生和20例前列腺癌患者血清中的特异性抗原、游离PSA,并计算f/tPSA比值。结果:血清PSA在4 ng/ml~10 ng/ml时,前列腺增生与前列腺癌组的特异性抗原含量差异无显著性(P0.05),游离PSA、f/tPSA比值差异具有显著性(P0.05)。结论:在前列腺增生和前列腺癌诊断灰区,tPSA作为筛选前列腺癌的临界值存在一定缺陷;联合测定tPSA、fPSAP、f/tPSA可明显提高对PCA诊断的特异性,特别是当tPSA为4.0~10.0μg/L诊断灰区时,f/t比值对诊断前列腺癌有重要的临床意义。

关 键 词:前列腺增生  前列腺癌  特异性抗原  f/tPSA

Diagnosis significance of relative value of f/tPSA for prostate cancer and bisectional prostate hypertrophy
XU Shao-guo,ZHU Lian-sheng.Diagnosis significance of relative value of f/tPSA for prostate cancer and bisectional prostate hypertrophy[J].Journal of Anhui Heaith Vocational & Technical College,2011,10(5):84-85.
Authors:XU Shao-guo  ZHU Lian-sheng
Institution:Bozhou People's Hospital,Bozhou 236800,Anhui
Abstract:Objective: It is to investigate the diagnosis significance of total prostate specific antigen(tPSA),free prostate specific antigen(fPSA)and f/tPSA for prostate cancer(PCA) and bisectional prostate hypertrophy(BHP) Methods: 20patients with PCa and 60 patients with benign prostatic hypertrophy(BPH) were diagnosed by pathobiology whose levelsof tPSA,andfPSA were examined in serums by Immunofluorecence assay(FIA).The results were analyzed.Results:When tPSA level isfrom 4.0-10.0μg/L in gray zone,The difference in serum tPSA between the twogroups was not significant(P0.05),but f/t of Pca group was significantly lower than that of BPHgroup(P0.05).Conclusion: benign prostatic hypertrophy and prostate cancer were in gray zone.It is unreasonable that tPSA is regarded as a critical value for the diagnosis of prostate carcinoma.When tPSA level is from 4.0-10.0μg/L in gray zone,f/ t ratio has a significant value for diagnosing PCA.
Keywords:benign prostatic hypertrophy  prostate cancer  Prostatespecific antigen  f/tPSA
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号