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类戈登分枝杆菌肺部疾病伴快速生长的孤立性病变:病例报告及文献复习。

Mycobacterium paragordonae pulmonary disease with rapidly growing solitary lesions: a case report and literature review.

机构信息

Department of Respiratory and Critical Care Medicine, Nanjing Yimin Hospital, Nanjing, Jiangsu Province, China.

Department of Pathology, Jinling Hospital, Nanjing, Jiangsu Province, China.

出版信息

J Infect Dev Ctries. 2024 Oct 31;18(10):1625-1631. doi: 10.3855/jidc.18664.

Abstract

INTRODUCTION

Mycobacterium paragordonae (MPG) is a novel and uncommon nontuberculous mycobacterium (NTM). We describe a case of MPG pulmonary disease (MPGPD) with a single, rapidly growing, pulmonary mass, which has rarely been reported.

CASE REPORT

A chest CT scan of a 66-year-old woman revealed a rapidly growing solitary mass-like lesion in the upper lobe of the right lung, which was not seen in the previous chest CT scan six months ago. H&E-stained section of the CT-guided percutaneous lung tissue biopsy specimen showed chronic inflammatory changes with epithelioid granulomas. Metagenomic next-generation sequencing (mNGS) of lung tissue biopsy specimen identified MPG with a sequence number of 1617 and a confidence level of 99%. Because the subsequent MPG droplet digital PCR (MPG-ddPCR) test of the lung tissue biopsy was positive, she was eventually diagnosed with MPGPD. She was administered a quadruple oral regimen comprising clarithromycin, levofloxacin, rifampicin, and ethambutol according to the ATS/IDSA protocol for Mycobacterium gordonae (MG) infection. The chest CT scans showed a significant reduction in the lesion one month after the treatment and almost complete resolution four months later.

CONCLUSIONS

MPGPD is a rare NTM infection. The imaging manifestations of MPGPD are diverse and may even show rapid development. mNGS of tissue biopsy can enable prompt diagnosis of MPG infection and is a good alternative to routine NTM microbial testing. The ATS/IDSA protocol for MG infection is an effective treatment for MPG infection.

摘要

介绍

分枝杆菌属(MPG)是一种新型且罕见的非结核分枝杆菌(NTM)。我们描述了一例 MPG 肺病(MPGPD),表现为单一、快速生长的肺部肿块,这种情况很少见。

病例报告

一名 66 岁女性的胸部 CT 扫描显示右上肺叶有一个快速生长的孤立性肿块样病变,而六个月前的胸部 CT 扫描未见该病变。CT 引导下经皮肺组织活检的 H&E 染色切片显示慢性炎症改变伴上皮样肉芽肿。肺组织活检的宏基因组下一代测序(mNGS)鉴定出 MPG,序列数为 1617,置信度为 99%。由于随后的肺组织活检 MPG 液滴数字 PCR(MPG-ddPCR)检测为阳性,最终诊断为 MPGPD。她接受了包含克拉霉素、左氧氟沙星、利福平、乙胺丁醇的四联口服方案治疗,该方案根据美国胸科学会/美国传染病学会(ATS/IDSA)制定的 MG 感染治疗方案。胸部 CT 扫描显示,治疗一个月后病变明显缩小,四个月后几乎完全缓解。

结论

MPGPD 是一种罕见的 NTM 感染。MPGPD 的影像学表现多种多样,甚至可能迅速发展。组织活检的 mNGS 可以快速诊断 MPG 感染,是常规 NTM 微生物检测的良好替代方法。ATS/IDSA 制定的 MG 感染治疗方案是治疗 MPG 感染的有效方法。

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