首页 | 本学科首页   官方微博 | 高级检索  
检索        

sFasL检测对结核性与恶性胸腔积液鉴别诊断价值的探讨
引用本文:刘玉峰,刘加洪,车文华,石玉桂.sFasL检测对结核性与恶性胸腔积液鉴别诊断价值的探讨[J].中国防痨通讯,2007,29(4):324-327.
作者姓名:刘玉峰  刘加洪  车文华  石玉桂
作者单位:1.青岛市胸科医院 青岛 266043;2.青岛市中心医院 青岛 266000;
摘    要:目的探讨sFasL对恶性胸腔积液与结核性胸腔积液鉴别诊断价值。方法应用ELISA法分别检测32例恶性胸腔积液和43例结核性胸腔积液中sFasL的含量,对结果进行统计学处理。结果结核性胸腔积液组sFasL(13.56±5.38 ng/ml)显著高于恶性胸腔积液组(5.72±2.59 ng/ml),二者具显著性差异(P<0.001)。以10 ng/ml为临界值,胸腔积液中sFasL>10 ng/ml诊断为结核性胸腔积液的敏感性为81.4%(35/43),特异性为81.3%(26/32),临床诊断符合率为81.4%(61/75)。结论sFasL对结核性、恶性胸腔积液的鉴别诊断有临床实用价值。

关 键 词:sFasL  恶性胸腔积液  结核性胸腔积液  酶联免疫吸附实验  
修稿时间:2006年10月19

Diagnostic values and clinical significance of detecting soluble FasL of pleural effusions in differentiating tuberculous and malignant pleural effusions
Liu Yufeng,Che Wenhua,Shi Yugui,et al..Diagnostic values and clinical significance of detecting soluble FasL of pleural effusions in differentiating tuberculous and malignant pleural effusions[J].The Journal of The Chinese Antituberculosis Association,2007,29(4):324-327.
Authors:Liu Yufeng  Che Wenhua  Shi Yugui  
Institution:1.Qingdao Chest Hospital of Shandong Province,Qingdao 266043,China
Abstract:Objective To explore the diagnostic values and clinical significance of detecting soluble FasL of pleural effusions in differentiating tuberculous and malignant pleural effusions.Methods Using enzyme-linked immunosorbent assay(ELISA) method to detect the soluble FasL in 43 tuberculous pleural effusions and 32 malignant pleural effusions.Results The mean of soluble FasL of tuberculous pleural effussions(13.56±5.38ng/ml)was markedly higher than that of malignant pleural effusions(5.72±2.59ng/ml)(P<0.001).If 10ng/ml of soluble FasL was regarded as cutoff value,the sensitivity,the specificity and accordance of diagnosing tuberculous pleural effusions were 81.4%,81.3% and 81.4%,respectively.Conclusion Soluble FasL might be a effective laboratory marks of differentiating tuberculous and malignant pleural effusions.
Keywords:sFasL
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《中国防痨通讯》浏览原始摘要信息
点击此处可从《中国防痨通讯》下载免费的PDF全文
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