Clinical Application of Polymerase Chain Reaction for the Diagnosis of Extrapulmonary Tuberculosis.
- Author:
Sang Sin PARK
;
Mi Ae LEE
;
Ki Sook HONG
- Publication Type:Original Article
- MeSH:
Ascitic Fluid;
Bone Marrow;
Cerebrospinal Fluid;
Clone Cells;
Diagnosis*;
Diagnostic Tests, Routine;
DNA;
Female;
Humans;
Lymph Nodes;
Mycobacterium tuberculosis;
Needles;
Polymerase Chain Reaction*;
Sensitivity and Specificity;
Sputum;
Tuberculosis*
- From:Korean Journal of Clinical Pathology
1997;17(1):79-88
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: There are many reports showing the efficacy of polymerase chain reaction(PCR) for the diagnosis of Mycobacterium tuberculosis in sputum. but only few reports in extrapulmonary specimens. Because of the difficulty in establishing a diagnosis of tuberculosis in the extrapulmonary specimens there have been considerable interest in the development of a rapid sensitive diagnostic test that might be useful. Therefore we used PCR for detection of M. tuberculosis DNA in extrapulmonary specimens and compared the results of conventional acid-fast stain, culture methods and PCR assay. METHODS: Total of 63 clinical samples(10 cerebrospinal fluids, 12 pleural fluids, 1 pericardial fluid, 3 bone marrow aspirates, 1 ascitic fluid, 25 fine needle aspirates of lymph nodes, 7 urine, 1 stool and 3 tissue biopsies) in Ewha Womans University Tongdaemun hospital were analysed by the PCR. We performed the PCR using a species-specific M. tuberculosis DNA fragment(mtp 40 gene) as primers that was cloned and sequenced at recent and a 396-bp fragment was specifically amplified. We analyzed sensitivity and specificity of AFB culture and PCR for the diagnosis of extrapulomonary tuberculosis. RESULTS: The positivity of AFB smear, culture and PCR were 2(10%), 4(20%), 13(65%) out of total 20 cases diagnosed as clinically active extrapulmonary tuberculosis. respectively. All of 2 smear-positive samples and 2 of 4 culture-positive and smear-negative samples were PCR-positive. And 9 of 14 smear and culture negative specimens also gave detectable DNA products in PCR The specificity of PCR(95.4%) is compared with those of smear and culture(100.0%). CONCLUSIONS: This results suggest that the PCR assay is a sensitive and rapid diagnostic alternative to classical procedures for the diagnosis of extrapulmonary tuberculosis.
