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Comparison of in house polymerase chain reaction with conventional techniques for the detection of Mycobacterium tuberculosis DNA in granulomatous lymphadenopathy

机译:室内聚合酶链反应与常规技术检测肉芽肿性淋巴结病结核分枝杆菌DNA的比较

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Aims—To evaluate the usefulness of the devR based polymerase chain reaction (PCR) in the detection of Mycobacterium tuberculosis in lymph node aspirates and tissues of lymphadenitis and to compare PCR with conventional diagnostic techniques. Subjects and methods—Coded specimens of fine needle aspirates and biopsies from 22 patients with tuberculous lymphadenitis, 14 patients with non-tubercular lymphadenitis, and nine patients with granulomatous lymphadenitis were processed and subjected to analysis by PCR, smear microscopy, M tuberculosis culture, histology, and cytology. Results—Tuberculous lymphadenitis was correctly diagnosed by PCR in 18 patients, by culture in five patients, by histology in 13 patients, and by cytology in seven patients. PCR gave two false positive results in 14 patients with non-tubercular lymphadenitis. The sensitivity of the conventional techniques was significantly higher with biopsies (17 of 22 specimens; 77%) than with fine needle aspirates (nine of 22 specimens; 41%). However, the sensitivity of PCR was not significantly higher with biopsies (68%) in comparison with fine needle aspirates (55%). The sensitivity of either biopsy PCR or fine needle aspirate PCR was not significantly different from that of either histology combined with culture or cytology combined with culture. The overall combined specificity of PCR was 86%. Mycobacterium tuberculosis DNA was detected in six of nine patients with granulomatous lymphadenitis. Conclusion—PCR is the most sensitive single technique available to date for the demonstration of M tuberculosis in specimens derived from patients with a clinical suspicion of tuberculous lymphadenitis. The value of PCR lies in its use as an adjunct test in the diagnosis of tuberculous lymphadenitis, particularly in those patients where conventional methods fail. Because fine needle aspiration is not an invasive procedure, it is the procedure of choice, and PCR should be performed initially on these samples. Excisional biopsy histology and PCR should be recommended only for patients in whom fine needle aspirate PCR is negative or when there is discrepancy with the clinical impression. >Key Words: Mycobacterium tuberculosis • devR polymerase chain reaction • tuberculous lymphadenitis
机译:目的—评估基于devR的聚合酶链反应(PCR)在检测淋巴结抽吸物和淋巴结炎组织中的结核分枝杆菌中的有用性,并将PCR与常规诊断技术进行比较。研究对象和方法:对22例结核性淋巴结炎,14例非结核性淋巴结炎和9例肉芽肿性淋巴结炎的细针抽吸和活检标本进行了处理,并进行了PCR,涂片显微镜检查,M结核培养,组织学分析和细胞学。结果:通过PCR对18例患者进行了结核性淋巴结炎的正确诊断,对5例进行了培养,对13例进行了组织学检查,对7例进行了细胞学检查。 PCR在14例非结核性淋巴结炎患者中给出了两个假阳性结果。活检的常规技术(22个样本中的17个; 77%)显着高于细针抽吸物(22个样本中的9个; 41%)的敏感性。但是,与细针抽吸物(55%)相比,活检(68%)的PCR敏感性没有明显提高。活检PCR或细针穿刺PCR的敏感性与组织学结合培养或细胞学结合培养均无显着差异。 PCR的总体组合特异性为86%。 9例肉芽肿性淋巴结炎患者中有6例检测到结核分枝杆菌DNA。结论—PCR是迄今为止可用于在临床怀疑结核性淋巴结炎患者样本中证明M结核病的最敏感的单一技术。 PCR的价值在于将其作为辅助测试来诊断结核性淋巴结炎,尤其是那些常规方法无效的患者。由于细针抽吸不是侵入性操作,因此是首选操作,应首先在这些样品上进行PCR。仅对于细针抽吸PCR阴性或临床印象有差异的患者,建议进行活检组织学和PCR。 >关键词:结核分枝杆菌•devR聚合酶链反应•结核性淋巴结炎

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