石蜡包埋组织实时荧光定量PCR技术在结核病诊断中的应用

被引:11
作者
娄丽萍 [1 ]
张文迪 [2 ]
机构
[1] 华中科技大学同济医学院附属同济医院病理研究所
[2] 华中科技大学同济医学院附属同济医院儿科
关键词
石蜡包埋组织; 结核病; 实时荧光定量PCR; 抗酸染色;
D O I
10.13847/j.cnki.lnmu.2019.03.023
中图分类号
R52 [结核病];
学科分类号
1002 ; 100201 ;
摘要
目的探讨石蜡包埋组织实时荧光定量PCR (RT-q PCR)检测结核分枝杆菌DNA在结核病诊断中的应用价值。方法收集58例临床确诊为结核病与40例非结核肉芽肿性疾病的石蜡包埋组织标本,应用RT-q PCR检测标本中结核分枝杆菌DNA,同时进行Ziehl-Neelsen抗酸染色,比较RT-q PCR与抗酸染色检测结果的差异。结果 58例结核病例中通过RT-q PCR检测有56例为阳性,灵敏度为96. 6%(56/58);通过抗酸染色检测有16例为阳性,灵敏度为27. 6%(16/58),两者灵敏度差异有统计学意义(P<0. 001)。而40例非结核性肉芽肿病例通过RT-q PCR检测有39例为阴性,特异度为97. 5%(39/40),通过抗酸染色检测有36例为阴性,特异度为90. 0%(36/40),两者特异度差异无统计学意义(P=0. 359)。结论相对结核抗酸染色,RT-q PCR灵敏度较高,是石蜡包埋组织快速检测结核分枝杆菌DNA的有效工具,是快速诊断结核病的重要手段。
引用
收藏
页码:74 / 76+119 +119
页数:4
相关论文
共 19 条
[1]  
Containment of Bioaerosol Infection Risk by the Xpert MTB/RIF Assay and Its Applicability to Point-of-Care Settings. Padmapriya P. Banada,Satheesh K. Sivasubramani,Robert Blakemore. Journal of Clinical Microbiology . 2010
[2]   《结核病分类》和《肺结核诊断》新标准对结核病控制工作的影响 [J].
姜世闻 .
中国防痨杂志, 2018, 40 (03) :229-230
[3]   PCR-荧光探针法快速诊断分枝杆菌属感染临床应用研究 [J].
郭莉娜 ;
徐英春 ;
孙宏莉 ;
宋红梅 ;
王瑶 ;
赵颖 .
中华医院感染学杂志, 2015, 25 (21) :4811-4813
[4]  
Rapid molecular detection of tuberculosis and rifampin resistance. CC Boehme,P Nabeta,D Hillemann,MP Nicol,S Shenai,F Krapp,J Allen,R Tahirli,R Blakemore,R Rustomjee,A Milovic,M Jones,SM O’Brien,DH Persing,S Ruesch-Gerdes,E Gotuzzo,C Rodrigues,D Alland,MD Perkins. The New England Quarterly . 2010
[5]  
Rapid diagnosis of mycobacterial infections and quantitation of Mycobacterium tuberculosis load by two real-time calibrated PCR assays. Broccolo Francesco,Scarpellini Paolo,Locatelli Giuseppe,Zingale Anna,Brambilla Anna M,Cichero Paola,Sechi Leonardo A,Lazzarin Adriano,Lusso Paolo,Malnati Mauro S. Journal of Clinical Microbiology . 2003
[6]  
Rapid and specific detection of Mycobacterium tuberculosis from acid-fast bacillus smear-positive respiratory specimens and BacT/ALERT MP culture bottles by using fluorogenic probes and real-time PCR. Miller Nancimae,Cleary Tim,Kraus Günter,Young Andrea K,Spruill Gina,Hnatyszyn H James. Journal of Clinical Microbiology . 2002
[7]  
Real-time PCR assay using fine-needle aspirates and tissue biopsy specimens for rapid diagnosis of mycobacterial lymphadenitis in children. Bruijnesteijn Van Coppenraet E S,Lindeboom J A,Prins J M,Peeters M F,Claas E C J,Kuijper E J. Journal of Clinical Microbiology . 2004
[8]  
WHO publishes Global tuberculosis report 2013. Eurosurveillance editorial team. Euro Surveillance Bulletin Europeen sur les Maladies Transmissibles . 2013
[9]  
Detection of mycobacterium tuberculosis complex in paraffin-embedded tissues by real-time fluorescent quantitative polymerase chain reaction. Ye F,Chen Y,He D,et al. Chinese Journal of Pathology . 2013
[10]  
Comparison of smear microscopy, culture, and real-time PCR for quantitative detection of Mycobacterium tuberculosis in clinical respiratory specimens[J] . Davood Darban-Sarokhalil,Abbas Ali Imani Fooladi,Parviz Maleknejad,Zakaria Bameri,Moloud Aflaki,Bizhan Nomanpour,Somayeh Yaslianifard,Mohammad Hossein Modarresi,Mohammad Mehdi Feizabadi. &nbspScandinavian Journal of Infectious Diseases . 2013 (4)