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

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TLDR
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 and should be recommended only for patients in whom fine needle aspirate PCR is negative.
Abstract
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

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TL;DR: Peripheral tuberculous lymphadenitis accounts for ~10% of tuberculosis cases in the United States and initial excisional biopsy deserves consideration for both optimal diagnosis and management of the otherwise slow response to therapy.
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TL;DR: A potential role for devR-devS in the regulation of genetic programmes unique to the tubercle bacillus is suggested.
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Peripheral tuberculous lymphadenitis: epidemiology, diagnosis, treatment, and outcome.

TL;DR: In this cohort, 101 patients received a final diagnosis of peripheral tuberculous lymphadenitis, and eighty-two percent received their entire therapy under direct observation, and response to antituberculous therapy was uniformly successful.
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TL;DR: Review of selected elementary statistics random sampling relative risk and odds ratio attributable risk adjustment of data without use of multivariate models and comparison of numerical results for various methods of adjustment the primacy of data collection.
Journal ArticleDOI

IS6110, an IS-like element of Mycobacterium tuberculosis complex.

TL;DR: Mobile genetic elements are useful genetic tools and have been found in most organisms which have been examined and will be used as probe for the identification of the M. tuberculosis complex.
Journal ArticleDOI

Large-scale use of polymerase chain reaction for detection of Mycobacterium tuberculosis in a routine mycobacteriology laboratory.

TL;DR: Investigation of the use of DNA amplification by the polymerase chain reaction reaction (PCR) for detection of Mycobacterium tuberculosis from clinical specimens found that no patient who had three of more sputum specimens tested would have been misdiagnosed.
Journal ArticleDOI

Peripheral lymph node tuberculosis: A review of 80 cases

TL;DR: One hundred and ninety‐two patients with peripheral lymphadenopathy were screened and 80 patients with tubercular lymphadenitis were studied; most were younger than 30 years and there was a slight female preponderance.
Journal ArticleDOI

Relevance of nucleic acid amplification techniques for diagnosis of respiratory tract infections in the clinical laboratory.

TL;DR: The efficiency of nucleic acid amplification techniques for the diagnosis of respiratory tract infections is reviewed and it is shown that the techniques can be useful for the rapid identification of M. tuberculosis in particular circumstances, as well as the rapid detection of most rifampin-resistant isolates.
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