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本文引用的文献

1
The Pharmacokinetics of Moxifloxacin in Cerebrospinal Fluid Following Intravenous Administration: A Report of Successfully Treated Infant with Mycoplasma hominis Meningitis.莫西沙星静脉给药后脑脊液药代动力学:成功治疗人型支原体脑膜炎婴儿的报告。
Pediatr Infect Dis J. 2020 Aug;39(8):e183-e184. doi: 10.1097/INF.0000000000002655.
2
An infant case with hydrocephalus as the initial manifestation of Mycoplasma hominis-associated meningitis.1例以脑积水为首发表现的人型支原体相关性脑膜炎婴儿病例。
J Infect Chemother. 2017 Oct;23(10):713-716. doi: 10.1016/j.jiac.2017.03.012. Epub 2017 Apr 10.
3
Neonate with Mycoplasma hominis meningoencephalitis given moxifloxacin.新生儿感染人型支原体脑膜炎给予莫西沙星治疗。
Lancet Infect Dis. 2016 Nov;16(11):e261-e266. doi: 10.1016/S1473-3099(16)30162-1. Epub 2016 Sep 16.
4
Molecular mechanism of fluoroquinolones resistance in Mycoplasma hominis clinical isolates.人型支原体临床分离株对氟喹诺酮类耐药的分子机制
Braz J Microbiol. 2014 May 19;45(1):239-42. doi: 10.1590/s1517-83822014000100034. eCollection 2014.
5
Clinical pharmacokinetics of antibacterials in cerebrospinal fluid.抗菌药物在脑脊液中的临床药代动力学。
Clin Pharmacokinet. 2013 Jul;52(7):511-42. doi: 10.1007/s40262-013-0062-9.
6
Mycoplasma hominis Meningitis in a 24 Week Premature Neonate: Case Report and Short Literature Review.24周早产儿人型支原体脑膜炎:病例报告及文献综述
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Pharmacokinetics of moxifloxacin in an infant with Mycoplasma hominis meningitis.莫西沙星在婴儿肺炎支原体脑膜炎中的药代动力学。
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In-vitro activities of tetracyclines, macrolides, fluoroquinolones and clindamycin against Mycoplasma hominis and Ureaplasma ssp. isolated in Germany over 20 years.20 多年来德国分离的人型支原体和脲原体对四环素类、大环内酯类、氟喹诺酮类和克林霉素的体外活性。
Clin Microbiol Infect. 2010 Nov;16(11):1649-55. doi: 10.1111/j.1469-0691.2009.03155.x.
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Clin Infect Dis. 2009 Oct 1;49(7):1080-2. doi: 10.1086/605576.
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Then and now: use of 16S rDNA gene sequencing for bacterial identification and discovery of novel bacteria in clinical microbiology laboratories.过去与现在:16S rDNA基因测序在临床微生物实验室细菌鉴定及新细菌发现中的应用
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人型支原体脑膜炎一例报告:极低出生体重儿病例

Mycoplasma hominis meningitis in an extremely preterm newborn: a case report.

机构信息

Department of Neonatology Sunnybrook Health Sciences Centre, University of Toronto, 2075 Bayview Avenue, M Wing, M4N 3M5, Toronto, Ontario, Canada.

出版信息

BMC Pediatr. 2021 Feb 8;21(1):69. doi: 10.1186/s12887-021-02532-3.

DOI:10.1186/s12887-021-02532-3
PMID:33557784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7869195/
Abstract

BACKGROUND

Mycoplasma Hominis is a micro-organism which is a part of the human genitourinary tract flora. Neonates are susceptible to acquire this pathogen either in utero or through vertical transmission. In rare cases, it may cause central nervous system infections with severe morbidity and mortality in preterm and term neonates.

CASE PRESENTATION

We present a case of Mycoplasma Hominis meningitis in an extremely preterm neonate who presented with lethargy, tachycardia and seizures on day 7 of life. There was no history of maternal systemic or genitourinary infection during pregnancy and at the time of delivery. Empirical antibiotic therapy for neonatal meningitis was commenced after sending blood and cerebrospinal fluid cultures. Cerebrospinal fluid analysis showed pleocytosis with neutrophilic predominance, but no bacteria was identified on gram staining. Blood culture yielded no growth of any bacterial pathogen. However, growth of Mycoplasma Hominis was suspected in cerebrospinal fluid culture which was confirmed by 16S ribosomal ribonucleic acid (RNA) polymerase chain reaction analysis. Subsequently, antibiotics were changed to Moxifloxacin and Doxycycline which were given for a total duration of 6 weeks. Multiple cerebrospinal fluid cultures were performed during this treatment. No growth of any pathogen was identified on any of these cerebrospinal fluid cultures.

CONCLUSIONS

We report a rare case of Mycoplasma Hominis meningitis in an extremely preterm neonate which was successfully treated with a combination therapy of Moxifloxacin and Doxycycline. It is important to consider the possibility of Mycoplasma Hominis meningitis in neonates who present with clinical signs and pleocytosis in cerebrospinal fluid but negative gram staining and no growth on conventional culture media.

摘要

背景

人型支原体是一种存在于人体泌尿生殖道的微生物。新生儿可在宫内或通过垂直传播感染这种病原体。在极少数情况下,它可能引起中枢神经系统感染,导致早产儿和足月儿严重发病和死亡。

病例介绍

我们报告了一例极其早产的新生儿人型支原体脑膜炎病例,该患儿在出生后第 7 天出现嗜睡、心动过速和惊厥。母亲在怀孕期间和分娩时均无全身或泌尿生殖道感染史。在发送血液和脑脊液培养物后,开始经验性治疗新生儿脑膜炎的抗生素。脑脊液分析显示白细胞增多,中性粒细胞为主,但革兰氏染色未发现细菌。血培养未生长任何细菌病原体。然而,怀疑脑脊液培养物中存在人型支原体生长,16S 核糖体核糖核酸(RNA)聚合酶链反应分析证实了这一点。随后,抗生素更换为莫西沙星和多西环素,总共治疗 6 周。在此治疗期间进行了多次脑脊液培养。这些脑脊液培养物均未发现任何病原体生长。

结论

我们报告了一例极其早产的新生儿人型支原体脑膜炎的罕见病例,该病例通过莫西沙星和多西环素联合治疗取得成功。对于出现临床症状和脑脊液白细胞增多但革兰氏染色阴性且常规培养物无生长的新生儿,应考虑人型支原体脑膜炎的可能性。