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一例由马格内分枝杆菌感染引起的小儿皮下脓肿。

A Case of Pediatric Subcutaneous Abscess Caused by Mycobacterium mageritense Infection.

机构信息

Department of Pediatrics , Nara Medical University, Japan.

Division of Infectious Diseases, The Hospital for Sick Children, Canada.

出版信息

Jpn J Infect Dis. 2021 Jul 21;74(4):377-380. doi: 10.7883/yoken.JJID.2020.621. Epub 2021 Jan 29.

DOI:10.7883/yoken.JJID.2020.621
PMID:33518619
Abstract

Soft tissue infections with Mycobacterium mageritense are uncommon. We report the case of a 5-year-old girl who developed a subcutaneous abscess in her right ankle caused by M. mageritense. She had a history of acute encephalopathy and adrenal insufficiency and was hospitalized for acute pancreatitis. During hospitalization, the patient developed fever and tachycardia. Blood culture was positive for gram-positive bacilli. Although initial testing with matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) reported a different organism, a repeat test identified M. mageritense. One month after the positive blood culture, she developed redness and swelling in the right ankle. The pus from the subcutaneous abscess after drainage grew M. mageritense, which was further confirmed by the sequencing of housekeeping genes. Based on sensitivity testing, the patient was treated with tosufloxacin and linezolid. The local inflammatory signs gradually improved on starting the treatment. The antibiotics were administered for 6 months, and she experienced no relapse during the 8 months of follow-up after the completion of therapy. This is the first case report of a pediatric M. mageritense infection, which also highlights an important potential pitfall of MALDI-TOF MS. Further, we observe that the choice of antimicrobials for the treatment of M. mageritense is more limited in children than in adults.

摘要

曼格分枝杆菌引起的软组织感染较为少见。我们报告了一例 5 岁女孩的病例,她的右脚踝出现皮下脓肿,由曼格分枝杆菌引起。她曾患有急性脑病和肾上腺功能不全,并因急性胰腺炎住院。住院期间,患者出现发热和心动过速。血培养阳性为革兰阳性杆菌。尽管基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)的初步检测报告了一种不同的病原体,但重复检测鉴定出了曼格分枝杆菌。在阳性血培养后 1 个月,她的右脚踝出现红肿。引流后的皮下脓肿脓液中生长出曼格分枝杆菌,管家基因测序进一步证实了这一点。根据药敏试验,患者接受托氟沙星和利奈唑胺治疗。开始治疗后,局部炎症迹象逐渐改善。抗生素治疗 6 个月,治疗完成后 8 个月的随访中无复发。这是首例儿童曼格分枝杆菌感染的病例报告,也突显了 MALDI-TOF MS 的一个重要潜在陷阱。此外,我们观察到儿童治疗曼格分枝杆菌的抗菌药物选择比成人更有限。

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