[腺苷脱氨酶系数对结核性渗出性胸膜炎的诊断价值]。

A E Shirinkina, L V Burukhina, A A Shurygin, E N Milashina
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引用次数: 0

摘要

作者检查了51例年龄37.74±2.17岁的结核性胸膜炎和年龄49.8±4.6岁的非特异性胸膜炎。第一组18例孤立性结核性渗出性胸膜炎。第二组13例结核合并结核性胸膜炎。第三组为10例非特异性渗出性胸膜炎。结核性渗出性胸膜炎中,卡他性支气管炎是气管-支气管树状病变的主要形式(n = 20(64.5%))。1、2、3组腺苷脱氨酶(ADA)活性分别为2.18 +/- 0.73、2.41 +/- 0.80和2.47 +/- 1.52 U/l。因此,单独测量支气管肺泡液ADA与其他参数在胸膜炎病因的鉴别诊断中没有信息价值。在分析参数时,引入了ADA系数(CADA),计算公式为:K(ADA) = ADA/cytosis。结核性胸膜炎患者的K(ADA)为0.65 +/- 0.17(孤立性结核性渗出性胸膜炎为0.52 +/-0.13,结核性渗出性胸膜炎合并肺结核为0.84 +/- 0.36 (p < 0.05),非特异性胸膜炎为0.20 +/- 0.06 (p < 0.05)。ADA系数为0.52或更高,证实了孤立性胸膜炎的结核病因,并允许在特异性和非特异性胸膜炎(伴或不伴肺改变)之间进行鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The diagnostic value of adenosine deaminase coefficient in patients with tuberculous exudative pleurisy].

The authors examined 51 patients aged 37.74 +/- 2.17 years who had tuberculous pleurisy and aged 49.8 +/- 4.6 years who had nonspecific pleurisy. Group 1 comprised 18 patients with isolated tuberculous exudative pleurisy. Group 2 included 13 patients with tuberculosis complicated by tuberculous pleurisy. Group 3 consisted of 10 patients with nonspecific exudative pleurisy. Catarrhal endobronchitis was the leading form of tracheo-broncheal tree lesion among patients with tuberculous exudative pleurisy (n = 20 (64.5%)). The activity of adenosine deaminase (ADA) was 2.18 +/- 0.73, 2.41 +/- 0.80, and 2.47 +/- 1.52 U/l in Groups 1, 2, and 3, respectively. Thus, the measurement of bronchoalveolar fluid ADA separately from other parameters is of no informative value in the differential diagnosis of the etiology of pleurisy. While analyzing the parameters, the authors introduced the coefficient of ADA (CADA) that was calculated using the formula: K(ADA) = ADA/cytosis. In patients with tuberculous pleurisy, K(ADA) was 0.65 +/- 0.17 (this was 0.52 +/-0.13 in isolated tuberculous exudative pleurisy and 0.84 +/- 0.36 in tuberculous exudative pleurisy complicated by pulmonary tuberculosis (p < 0.05), and 0.20 +/- 0.06 in nonspecific pleurisy (p < 0.05). The ADA coefficient of 0.52 or more confirms the tuberculous etiology in isolated pleurisies and permits a differential diagnosis to be made between specific and nonspecific pleurisy with and without lung changes.

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