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宏基因组分析鉴定一名非HIV免疫功能低下患者的多微生物肺部感染:病例报告

Metagenomic analysis identifying a polymicrobial pulmonary infection in a non-HIV immunocompromised patient: a case report.

作者信息

Duan Jing, Ding Jie, Wei Yupeng, Zhang Yingxin, You Zhiqing, Li Ding, Chen Chao

机构信息

Department of Clinical Laboratory, Liaocheng People's Hospital and Liaocheng School of Clinical Medicine, Shandong First Medical University, Liaocheng, Shandong, 252000, China.

Central Laboratory, Liaocheng People's Hospital and Liaocheng School of Clinical Medicine, Shandong First Medical University, Liaocheng, Shandong, 252000, China.

出版信息

BMC Pulm Med. 2025 Jan 9;25(1):12. doi: 10.1186/s12890-024-03473-0.

Abstract

BACKGROUND

Polymicrobial pulmonary infections, common in immunocompromised patients, often manifest more severe symptoms than monomicrobial infections. Clinical diagnosis delays may lead to mortality, emphasizing the importance of fast and accurate diagnosis for these patients. Metagenomic next-generation sequencing (mNGS), as an unbiased method capable of detecting all microbes, is a valuable tool to identify pathogens, particularly in cases where infections are difficult to diagnosis using conventional methods.

CASE PRESENTATION

A 50-year-old male patient was admitted due to cough, expectoration and dyspnea. CT scan revealed diffuse inflammatory and cavernous lung lesion, and blood examination suggested a polymicrobial infection. However, no etiology was found by routine examination. mNGS of bronchoalveolar lavage fluid(BALF)simultaneously detected the presence of Pneumocystis jirovecii (P.jirovecii), Aspergillus fumigates (A.fumigates), Nocardia farcinica (N.farcinica), Salmonella enterica subsp. enterica (S.enterica subsp. enterica), and cytomegalovirus (CMV). The patient was successfully treated with compound sulfamethoxazole (SMZ-TMP), cefoperazone/sulbactam (SCF), moxifloxacin (MXF), voriconazole (VCZ), and ganciclovir. The patient recovered after two weeks of anti-infection therapy and maintained good health at a six-month follow-up.

CONCLUSION

For immunocompromised patients with multiple infections and atypical symptoms, mNGS emerged as a reliable approach to pathogen detection and guiding antibiotic therapy.

摘要

背景

多微生物肺部感染在免疫功能低下患者中很常见,通常比单微生物感染表现出更严重的症状。临床诊断延迟可能导致死亡,这凸显了对这些患者进行快速准确诊断的重要性。宏基因组下一代测序(mNGS)作为一种能够检测所有微生物的无偏方法,是识别病原体的宝贵工具,特别是在使用传统方法难以诊断感染的情况下。

病例报告

一名50岁男性患者因咳嗽、咳痰和呼吸困难入院。CT扫描显示弥漫性炎症和肺空洞病变,血液检查提示多微生物感染。然而,常规检查未发现病因。支气管肺泡灌洗液(BALF)的mNGS同时检测到耶氏肺孢子菌(P.jirovecii)、烟曲霉(A.fumigates)、鼻疽诺卡菌(N.farcinica)、肠炎沙门氏菌肠炎亚种(S.enterica subsp. enterica)和巨细胞病毒(CMV)的存在。患者接受复方磺胺甲恶唑(SMZ-TMP)、头孢哌酮/舒巴坦(SCF)、莫西沙星(MXF)、伏立康唑(VCZ)和更昔洛韦成功治疗。抗感染治疗两周后患者康复,六个月随访时保持健康。

结论

对于患有多种感染和非典型症状的免疫功能低下患者,mNGS成为病原体检测和指导抗生素治疗的可靠方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d84/11720941/a1ab5665848f/12890_2024_3473_Fig1_HTML.jpg

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