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Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature
Introduction. Moraxella nonliquefaciens is an unusual organism to be isolated from cerebral spinal fluid (CSF) and there exists only one case report of M. nonliquefaciens meningitis from a neonate. Moraxella species normally exist as part of the human upper respiratory tract flora and rarely cause i...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Microbiology Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361638/ https://www.ncbi.nlm.nih.gov/pubmed/28348808 http://dx.doi.org/10.1099/jmmcr.0.005086 |
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author | Kao, Carol Szymczak, Wendy Munjal, Iona |
author_facet | Kao, Carol Szymczak, Wendy Munjal, Iona |
author_sort | Kao, Carol |
collection | PubMed |
description | Introduction. Moraxella nonliquefaciens is an unusual organism to be isolated from cerebral spinal fluid (CSF) and there exists only one case report of M. nonliquefaciens meningitis from a neonate. Moraxella species normally exist as part of the human upper respiratory tract flora and rarely cause invasive human disease. There are only a handful of case reports implicating the organism as a cause of endocarditis, bacteraemia, septic arthritis and endophthalmitis. Identification to the species level based on routine laboratory techniques has been challenging, with final identification often made through 16S rRNA sequencing. With the use of a newer diagnostic tool, matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) MS, we were able to rapidly identify the organism and initiate appropriate treatment. Case presentation. We present a rare care of M. nonliquefaciens meningitis in a paediatric patient with an underlying cranial anatomical defect due to Crouzon syndrome. She had been admitted to hospital 3 months previously with Streptococcus pneumoniae meningitis and mastoiditis, and returned to the emergency department with meningismus. CSF culture grew M. nonliquefaciens. She was treated with ceftriaxone with rapid improvement and eventually was taken for endoscopic surgical repair of a right encephalocele defect. Conclusion. The use of MALDI-TOF MS allowed for the rapid identification of the organism. The patient recovered with appropriate antimicrobial therapy and eventual surgical correction. An underlying anatomical defect should be considered in all patients who present with meningitis due to this unusual organism. |
format | Online Article Text |
id | pubmed-5361638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-53616382017-03-27 Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature Kao, Carol Szymczak, Wendy Munjal, Iona JMM Case Rep Case Report Introduction. Moraxella nonliquefaciens is an unusual organism to be isolated from cerebral spinal fluid (CSF) and there exists only one case report of M. nonliquefaciens meningitis from a neonate. Moraxella species normally exist as part of the human upper respiratory tract flora and rarely cause invasive human disease. There are only a handful of case reports implicating the organism as a cause of endocarditis, bacteraemia, septic arthritis and endophthalmitis. Identification to the species level based on routine laboratory techniques has been challenging, with final identification often made through 16S rRNA sequencing. With the use of a newer diagnostic tool, matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) MS, we were able to rapidly identify the organism and initiate appropriate treatment. Case presentation. We present a rare care of M. nonliquefaciens meningitis in a paediatric patient with an underlying cranial anatomical defect due to Crouzon syndrome. She had been admitted to hospital 3 months previously with Streptococcus pneumoniae meningitis and mastoiditis, and returned to the emergency department with meningismus. CSF culture grew M. nonliquefaciens. She was treated with ceftriaxone with rapid improvement and eventually was taken for endoscopic surgical repair of a right encephalocele defect. Conclusion. The use of MALDI-TOF MS allowed for the rapid identification of the organism. The patient recovered with appropriate antimicrobial therapy and eventual surgical correction. An underlying anatomical defect should be considered in all patients who present with meningitis due to this unusual organism. Microbiology Society 2017-02-28 /pmc/articles/PMC5361638/ /pubmed/28348808 http://dx.doi.org/10.1099/jmmcr.0.005086 Text en 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Kao, Carol Szymczak, Wendy Munjal, Iona Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title | Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title_full | Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title_fullStr | Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title_full_unstemmed | Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title_short | Meningitis due to Moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
title_sort | meningitis due to moraxella nonliquefaciens in a paediatric patient: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361638/ https://www.ncbi.nlm.nih.gov/pubmed/28348808 http://dx.doi.org/10.1099/jmmcr.0.005086 |
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