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Neuroborreliosis with involvement of rhombencephalon: A case report

We describe a case of a 52 year-old woman who was hospitalized with rhombencephalitis caused by Borrelia burgdorferi sensu lato. The patient presented with intermittent fever, dry cough, fatigue, global headache, night sweats, unintentional weight loss, and neurological symptoms like diplopia, tremo...

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Detalles Bibliográficos
Autores principales: Svingen, Hilde, Orrem, Jon, Nørgaard Eskesen, Arne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938859/
https://www.ncbi.nlm.nih.gov/pubmed/35330755
http://dx.doi.org/10.1016/j.idcr.2022.e01472
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author Svingen, Hilde
Orrem, Jon
Nørgaard Eskesen, Arne
author_facet Svingen, Hilde
Orrem, Jon
Nørgaard Eskesen, Arne
author_sort Svingen, Hilde
collection PubMed
description We describe a case of a 52 year-old woman who was hospitalized with rhombencephalitis caused by Borrelia burgdorferi sensu lato. The patient presented with intermittent fever, dry cough, fatigue, global headache, night sweats, unintentional weight loss, and neurological symptoms like diplopia, tremor, paresthesia and ataxia. Examination of serum and cerebrospinal fluid (CSF) revealed positive Borrelia burgdorferi-specific antibody index and presence of CSF oligoclonal IgG bands, indicating intrathecal synthesis of Borrelia-specific antibodies. The clinical and biochemical picture thus suggested neuroborreliosis. Unexpectedly a magnetic resonance imaging (MRI) scan demonstrated inflammation in rhombencephalon that are extremely rare in patients with neuroborreliosis. The patient was treated with intravenous ceftriaxone with rapid improvement of her symptoms. The MRI findings were in regress six weeks after onset of antibiotic treatment, and normalized after about seven months.
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spelling pubmed-89388592022-03-23 Neuroborreliosis with involvement of rhombencephalon: A case report Svingen, Hilde Orrem, Jon Nørgaard Eskesen, Arne IDCases Case Report We describe a case of a 52 year-old woman who was hospitalized with rhombencephalitis caused by Borrelia burgdorferi sensu lato. The patient presented with intermittent fever, dry cough, fatigue, global headache, night sweats, unintentional weight loss, and neurological symptoms like diplopia, tremor, paresthesia and ataxia. Examination of serum and cerebrospinal fluid (CSF) revealed positive Borrelia burgdorferi-specific antibody index and presence of CSF oligoclonal IgG bands, indicating intrathecal synthesis of Borrelia-specific antibodies. The clinical and biochemical picture thus suggested neuroborreliosis. Unexpectedly a magnetic resonance imaging (MRI) scan demonstrated inflammation in rhombencephalon that are extremely rare in patients with neuroborreliosis. The patient was treated with intravenous ceftriaxone with rapid improvement of her symptoms. The MRI findings were in regress six weeks after onset of antibiotic treatment, and normalized after about seven months. Elsevier 2022-03-08 /pmc/articles/PMC8938859/ /pubmed/35330755 http://dx.doi.org/10.1016/j.idcr.2022.e01472 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Svingen, Hilde
Orrem, Jon
Nørgaard Eskesen, Arne
Neuroborreliosis with involvement of rhombencephalon: A case report
title Neuroborreliosis with involvement of rhombencephalon: A case report
title_full Neuroborreliosis with involvement of rhombencephalon: A case report
title_fullStr Neuroborreliosis with involvement of rhombencephalon: A case report
title_full_unstemmed Neuroborreliosis with involvement of rhombencephalon: A case report
title_short Neuroborreliosis with involvement of rhombencephalon: A case report
title_sort neuroborreliosis with involvement of rhombencephalon: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938859/
https://www.ncbi.nlm.nih.gov/pubmed/35330755
http://dx.doi.org/10.1016/j.idcr.2022.e01472
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