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Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report

BACKGROUND: During fulminant meningococcal septicaemia, meningococci are often observed in the cerebrospinal fluid (CSF) although the patients have frequently no meningeal symptoms. Meningococcal meningitis, by contrast, usually features clinical meningeal signs and biochemical markers of inflammati...

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Autores principales: Hage-Sleiman, Mehdi, Derre, Nicolas, Verdet, Charlotte, Pialoux, Gilles, Gaudin, Olivier, Senet, Patricia, Fartoukh, Muriel, Boissan, Mathieu, Garnier, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419487/
https://www.ncbi.nlm.nih.gov/pubmed/30871501
http://dx.doi.org/10.1186/s12879-019-3866-x
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author Hage-Sleiman, Mehdi
Derre, Nicolas
Verdet, Charlotte
Pialoux, Gilles
Gaudin, Olivier
Senet, Patricia
Fartoukh, Muriel
Boissan, Mathieu
Garnier, Marc
author_facet Hage-Sleiman, Mehdi
Derre, Nicolas
Verdet, Charlotte
Pialoux, Gilles
Gaudin, Olivier
Senet, Patricia
Fartoukh, Muriel
Boissan, Mathieu
Garnier, Marc
author_sort Hage-Sleiman, Mehdi
collection PubMed
description BACKGROUND: During fulminant meningococcal septicaemia, meningococci are often observed in the cerebrospinal fluid (CSF) although the patients have frequently no meningeal symptoms. Meningococcal meningitis, by contrast, usually features clinical meningeal signs and biochemical markers of inflammation with elevated white blood cell count (pleiocytosis) in the CSF. Cases of typical symptomatic meningitis without these biochemical features are uncommon in adults. CASE PRESENTATION: A 21-year-old male presented with meningococcal purpura fulminans and disseminated intravascular coagulation (DIC) associated with multiple organ dysfunction syndrome requiring hospitalization in the Intensive Care Unit. Despite typical meningeal clinical signs, lumbar puncture showed no pleiocytosis, normal glycorachia and normal proteinorachia, whereas the lactate concentration in the CSF was high (5.8 mmol/L). CSF culture showed a high inoculum of serogroup C meningococci. On day 2, after initial improvement, a recurrence of hypotension led to the diagnosis of acute meningococcal myocarditis, which evolved favourably within a week. During the hospitalization, distal ischemic and necrotic lesions were observed, predominantly on the fingertips, which were treated with local and systemic vasodilators. CONCLUSIONS: We report a rare case of adult meningococcal disease characterized by an intermediate form of meningitis between purulent meningitis and meningeal inoculation from fulminant meningococcal septicaemia, without classical signs of biological inflammation. It highlights the diagnostic value of CSF lactate, which may warrant administration of a meningeal dosing regimen of beta-lactam antibiotics. This case also demonstrates the potential severity of meningococcal myocarditis; we discuss its pathophysiology, which is distinct from other sepsis-related cardiomyopathies. Finally, the observed effects of vasodilators on the meningococcal skin ischemia in this case encourages future studies to assess their efficacy in DIC-associated necrosis.
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spelling pubmed-64194872019-03-28 Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report Hage-Sleiman, Mehdi Derre, Nicolas Verdet, Charlotte Pialoux, Gilles Gaudin, Olivier Senet, Patricia Fartoukh, Muriel Boissan, Mathieu Garnier, Marc BMC Infect Dis Case Report BACKGROUND: During fulminant meningococcal septicaemia, meningococci are often observed in the cerebrospinal fluid (CSF) although the patients have frequently no meningeal symptoms. Meningococcal meningitis, by contrast, usually features clinical meningeal signs and biochemical markers of inflammation with elevated white blood cell count (pleiocytosis) in the CSF. Cases of typical symptomatic meningitis without these biochemical features are uncommon in adults. CASE PRESENTATION: A 21-year-old male presented with meningococcal purpura fulminans and disseminated intravascular coagulation (DIC) associated with multiple organ dysfunction syndrome requiring hospitalization in the Intensive Care Unit. Despite typical meningeal clinical signs, lumbar puncture showed no pleiocytosis, normal glycorachia and normal proteinorachia, whereas the lactate concentration in the CSF was high (5.8 mmol/L). CSF culture showed a high inoculum of serogroup C meningococci. On day 2, after initial improvement, a recurrence of hypotension led to the diagnosis of acute meningococcal myocarditis, which evolved favourably within a week. During the hospitalization, distal ischemic and necrotic lesions were observed, predominantly on the fingertips, which were treated with local and systemic vasodilators. CONCLUSIONS: We report a rare case of adult meningococcal disease characterized by an intermediate form of meningitis between purulent meningitis and meningeal inoculation from fulminant meningococcal septicaemia, without classical signs of biological inflammation. It highlights the diagnostic value of CSF lactate, which may warrant administration of a meningeal dosing regimen of beta-lactam antibiotics. This case also demonstrates the potential severity of meningococcal myocarditis; we discuss its pathophysiology, which is distinct from other sepsis-related cardiomyopathies. Finally, the observed effects of vasodilators on the meningococcal skin ischemia in this case encourages future studies to assess their efficacy in DIC-associated necrosis. BioMed Central 2019-03-12 /pmc/articles/PMC6419487/ /pubmed/30871501 http://dx.doi.org/10.1186/s12879-019-3866-x Text en © The Author(s). 2019 Open AccessThis article is distributed 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 you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Hage-Sleiman, Mehdi
Derre, Nicolas
Verdet, Charlotte
Pialoux, Gilles
Gaudin, Olivier
Senet, Patricia
Fartoukh, Muriel
Boissan, Mathieu
Garnier, Marc
Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title_full Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title_fullStr Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title_full_unstemmed Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title_short Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
title_sort meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419487/
https://www.ncbi.nlm.nih.gov/pubmed/30871501
http://dx.doi.org/10.1186/s12879-019-3866-x
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