Mycobacterium mageritense submandibular lymphadenitis in children: diagnostic challenges and the role of metagenomic next-generation sequencing: two case reports and literature review.

IF 3.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Frontiers in Medicine Pub Date : 2026-10-07 eCollection Date: 2026-01-01 DOI:10.3389/fmed.2026.1936269
Li Li, Zhijie Xing, Liyan Liu, Xiao Mu, Yunpeng Zhai, Shengwei Luan, Jian Li, Qingwei Guo
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引用次数: 0

Abstract

Mycobacterium mageritense is an extremely rare, rapidly growing nontuberculous mycobacterium (NTM). Pediatric cases are rarely reported worldwide, and the non-specific clinical manifestations, low sensitivity of conventional microbiological tests, and limited specimen volume from children often lead to diagnostic delays. We describe the clinical data of two immunocompetent children with submandibular lymphadenitis caused by Mycobacterium mageritense, both diagnosed by metagenomic next-generation sequencing (mNGS). We also systematically reviewed the relevant literature and performed a pooled analysis of 36 eligible cases (the two new paediatric cases from the present study included). Case 1 involved a 6-year-old girl with dental caries and acute fever who was initially misdiagnosed with common bacterial infection and received ineffective empirical antibiotics for over two weeks; mNGS of aspirated pus confirmed the diagnosis. Case 2 involved a 9-year-old girl with dental caries who presented only with submandibular lymphadenopathy and normal laboratory findings, with a diagnostic delay of up to two months; mNGS of lymph node tissue identified the pathogen. Literature-pooled analysis of 36 patients revealed a mean diagnostic delay of 4.69 months (median 2.00 months, IQR: 0.81-5.75 months). Conventional culture had low sensitivity, often requiring prolonged incubation (≥96 h) or special media to obtain positive results. Initial misdiagnosis occurred in 17.6% of cases. Patients diagnosed by NGS achieved more rapid and accurate pathogen identification. This report suggests that mNGS, as a culture-independent, unbiased pan-pathogen detection technique, shows clear advantages in identifying rare and fastidious pathogens such as M. mageritense. For pediatric patients with dental caries, fever, and cervical lymphadenopathy unresponsive to conventional therapy, clinicians should suspect Mycobacterium mageritense infection, and mNGS is an effective tool for its rapid and accurate diagnosis.

儿童马氏分枝杆菌下颌下淋巴结炎:诊断挑战和新一代宏基因组测序的作用:两个病例报告和文献综述。
马氏分枝杆菌是一种极为罕见、生长迅速的非结核分枝杆菌(NTM)。儿童病例在世界范围内很少报告,非特异性临床表现,传统微生物检测的低敏感性以及儿童标本量有限往往导致诊断延误。我们描述了两名免疫功能正常的儿童颌下腺炎由马格里氏分枝杆菌引起的临床资料,他们都是通过宏基因组新一代测序(mNGS)诊断出来的。我们还系统地回顾了相关文献,并对36例符合条件的病例(包括本研究中的2例新儿科病例)进行了汇总分析。病例1为一名患有龋齿和急性发热的6岁女童,最初被误诊为常见细菌感染,并接受了两周以上无效的经验性抗生素治疗;抽吸脓液的mNGS证实了诊断。病例2涉及一名患有龋齿的9岁女孩,仅表现为下颌下淋巴结病变和实验室检查结果正常,诊断延迟长达两个月;淋巴结组织的mNGS鉴定病原体。36例患者的文献汇总分析显示,平均诊断延迟4.69个月(中位2.00个月,IQR: 0.81-5.75个月)。常规培养灵敏度较低,通常需要长时间孵育(≥96 h)或特殊培养基才能获得阳性结果。最初误诊率为17.6%。采用NGS诊断的患者病原菌鉴定更加快速准确。该报告表明,mNGS作为一种不依赖于培养的、无偏倚的泛病原体检测技术,在鉴定马氏分枝杆菌等罕见和挑剔的病原体方面具有明显的优势。对于常规治疗无效的龋齿、发热、颈淋巴肿大患儿,临床医生应怀疑马格利特分枝杆菌感染,mNGS是快速准确诊断的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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