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肺结核分枝杆菌与 whipplei 热带菌合并肺部感染:一例报告。

Pulmonary coinfection of Mycobacterium tuberculosis and Tropheryma whipplei: a case report.

机构信息

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 200021, China.

Shanghai Guanghua Hosptial of Integrated Traditional Chinese and Western Medicine, Shanghai, 200052, China.

出版信息

J Med Case Rep. 2021 Jul 9;15(1):359. doi: 10.1186/s13256-021-02899-y.

Abstract

BACKGROUND

We diagnosed a clinical case of pulmonary infection involving Mycobacterium tuberculosis and Tropheryma whipplei in a patient with acute respiratory distress syndrome. The diagnosis was assisted by metagenomic next-generation sequencing of bronchoalveolar lavage fluid.

CASE PRESENTATION

A 44-year-old Han Chinese inmate was transferred to the emergency department because of dry cough, chest tightness, and shortness of breath. The patient's body temperature rose to 39.3 °C following empirical cephalosporin treatment for 1 week. The blood CD4+/CD8+ ratio was 0.7, suggesting immunodeficiency. Routine microbiological tests were performed, and tuberculosis interferon gamma release assays were positive. Mycobacterium tuberculosis polymerase chain reaction was also positive. Chest computed tomography scan revealed miliary nodules and ground-glass opacifications, which were in accordance with tuberculosis. To fully examine the etiology, we performed routine laboratory tests and metagenomic sequencing, the results of which indicated the presence of Mycobacterium tuberculosis and Tropheryma whipplei. We administered anti-tuberculosis regimen in combination with trimethoprim/sulfamethoxazole. The patient recovered, with chest computed tomography scan showing absorption of lesions.

CONCLUSIONS

Compared with traditional diagnostic methods such as culture and serology, metagenomic next-generation sequencing has the advantage of detecting a wide array of microorganisms in a single test and therefore can be used for clinical diagnosis of rare pathogens and microbial coinfections. It is particularly useful for immunocompromised patients as they are more prone to infection by opportunistic microorganisms.

摘要

背景

我们诊断了一例急性呼吸窘迫综合征患者的肺部感染病例,涉及分枝杆菌和旋毛虫。该诊断得到了支气管肺泡灌洗液宏基因组下一代测序的辅助。

病例介绍

一名 44 岁的汉族囚犯因干咳、胸闷和呼吸急促而被转至急诊部。在接受了 1 周的经验性头孢菌素治疗后,患者体温升高至 39.3°C。血 CD4+/CD8+比值为 0.7,提示免疫缺陷。进行了常规微生物学检查,结核干扰素γ释放试验阳性。分枝杆菌聚合酶链反应也呈阳性。胸部计算机断层扫描显示粟粒结节和磨玻璃影,符合肺结核。为了全面检查病因,我们进行了常规实验室检查和宏基因组测序,结果表明存在分枝杆菌和旋毛虫。我们给予抗结核方案联合甲氧苄啶/磺胺甲恶唑治疗。患者康复,胸部计算机断层扫描显示病变吸收。

结论

与培养和血清学等传统诊断方法相比,宏基因组下一代测序具有在单次检测中检测多种微生物的优势,因此可用于罕见病原体和微生物混合感染的临床诊断。对于免疫功能低下的患者尤其有用,因为他们更容易感染机会性微生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0130/8272354/0a3a48f2077c/13256_2021_2899_Fig1_HTML.jpg

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