Takagi N, Hasegawa Y, Ichiyama S, Shibagaki T, Shimokata K
First Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Int J Tuberc Lung Dis. 1998 Apr;2(4):338-41.
Government-administered regional teaching hospital.
To improve timeliness and sensitivity of laboratory diagnosis of tuberculous pleuritis.
We applied polymerase chain reaction (PCR) to detect DNA (IS6110) specific for Mycobacterium tuberculosis complex in pleural biopsy specimens.
Of 28 patients with pleural disease, 11 were diagnosed by microbiology (smear/culture of sputum or pleural fluid) with tuberculous pleuritis, eight were diagnosed with tuberculous pleuritis by histology (of pleural biopsies) and/or clinical presentation, and nine were diagnosed with carcinomatous pleuritis. Seventeen of the patients' pleural biopsies were PCR positive. Based on microbiological results, the sensitivity of the PCR assay was 100% (11/11). On the other hand, based on the results of the histological and clinical data, sensitivity and specificity of the PCR results were 89% (17/19) and 100% (9/9), respectively.
PCR of pleural biopsy specimens can be a useful method when employed in combination with microbiological and histological examinations of pleural biopsy for rapid diagnosis of tuberculous pleuritis.
政府管理的区域教学医院。
提高结核性胸膜炎实验室诊断的及时性和敏感性。
我们应用聚合酶链反应(PCR)检测胸膜活检标本中结核分枝杆菌复合群特异的DNA(IS6110)。
28例胸膜疾病患者中,11例通过微生物学检查(痰或胸腔积液涂片/培养)诊断为结核性胸膜炎,8例通过组织学检查(胸膜活检)和/或临床表现诊断为结核性胸膜炎,9例诊断为癌性胸膜炎。17例患者的胸膜活检标本PCR呈阳性。基于微生物学结果,PCR检测的敏感性为100%(11/11)。另一方面,基于组织学和临床数据结果,PCR结果的敏感性和特异性分别为89%(17/19)和100%(9/9)。
胸膜活检标本的PCR与胸膜活检的微生物学和组织学检查联合应用时,可作为快速诊断结核性胸膜炎的有用方法。