MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome

Abstract Background The presence of circulating anti-myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) has been described in sera of patients with different inflammatory conditions of the central nervous system. In adults the core clinical feature is usually characterised by acute myelitis an...

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Main Authors: Sara Mariotto, Salvatore Monaco, Patrick Peschl, Ilaria Coledan, Romualdo Mazzi, Romana Höftberger, Markus Reindl, Sergio Ferrari
Format: Article
Language:English
Published: BMC 2017-10-01
Series:BMC Neurology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12883-017-0971-6
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author Sara Mariotto
Salvatore Monaco
Patrick Peschl
Ilaria Coledan
Romualdo Mazzi
Romana Höftberger
Markus Reindl
Sergio Ferrari
author_facet Sara Mariotto
Salvatore Monaco
Patrick Peschl
Ilaria Coledan
Romualdo Mazzi
Romana Höftberger
Markus Reindl
Sergio Ferrari
author_sort Sara Mariotto
collection DOAJ
description Abstract Background The presence of circulating anti-myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) has been described in sera of patients with different inflammatory conditions of the central nervous system. In adults the core clinical feature is usually characterised by acute myelitis and/or optic neuritis. We here report an atypical case with serum and cerebrospinal fluid MOG-Abs and a clinical picture suggestive for acute encephalitis. Case presentation A 31-year-old Indian man presented with altered mental status, slight fever, and ataxia. Brain magnetic resonance imaging noted a widespread involvement of the white matter associated with slight cortical and subcortical damage in absence of contrast enhancement. An extensive infectious screening resulted negative while autoimmune analysis revealed the presence of MOG-Abs, detected with live cell-based assay. After treatment with intravenous immunoglobulins a marked and prompt clinical and radiological improvement was observed. Conclusions To date, several areas of uncertainty still remain regarding clinical features and prognosis of subjects with MOG-Abs. The description of atypical cases is crucial, since recognition of this condition leads to prompt treatment and better prognosis, as in the case here reported.
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spelling doaj.art-78b073234f2d45b590fb4a9338c5c61c2022-12-22T02:40:13ZengBMCBMC Neurology1471-23772017-10-011711610.1186/s12883-017-0971-6MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndromeSara Mariotto0Salvatore Monaco1Patrick Peschl2Ilaria Coledan3Romualdo Mazzi4Romana Höftberger5Markus Reindl6Sergio Ferrari7Department of Neuroscience, Biomedicine and Movement Sciences, Section of Neurology, University of VeronaDepartment of Neuroscience, Biomedicine and Movement Sciences, Section of Neurology, University of VeronaClinical Department of Neurology, Medical University of InnsbruckDepartment of Diagnostics and Public Health, Section of Infectious Diseases, University of VeronaDepartment of Diagnostics and Public Health, Section of Infectious Diseases, University of VeronaInstitute of Neurology, Medical University of ViennaClinical Department of Neurology, Medical University of InnsbruckDepartment of Neuroscience, Biomedicine and Movement Sciences, Section of Neurology, University of VeronaAbstract Background The presence of circulating anti-myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) has been described in sera of patients with different inflammatory conditions of the central nervous system. In adults the core clinical feature is usually characterised by acute myelitis and/or optic neuritis. We here report an atypical case with serum and cerebrospinal fluid MOG-Abs and a clinical picture suggestive for acute encephalitis. Case presentation A 31-year-old Indian man presented with altered mental status, slight fever, and ataxia. Brain magnetic resonance imaging noted a widespread involvement of the white matter associated with slight cortical and subcortical damage in absence of contrast enhancement. An extensive infectious screening resulted negative while autoimmune analysis revealed the presence of MOG-Abs, detected with live cell-based assay. After treatment with intravenous immunoglobulins a marked and prompt clinical and radiological improvement was observed. Conclusions To date, several areas of uncertainty still remain regarding clinical features and prognosis of subjects with MOG-Abs. The description of atypical cases is crucial, since recognition of this condition leads to prompt treatment and better prognosis, as in the case here reported.http://link.springer.com/article/10.1186/s12883-017-0971-6Autoimmune diseasesEncephalitisAnti-myelin oligodendrocyte glycoprotein antibodies (MOG-abs)
spellingShingle Sara Mariotto
Salvatore Monaco
Patrick Peschl
Ilaria Coledan
Romualdo Mazzi
Romana Höftberger
Markus Reindl
Sergio Ferrari
MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
BMC Neurology
Autoimmune diseases
Encephalitis
Anti-myelin oligodendrocyte glycoprotein antibodies (MOG-abs)
title MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
title_full MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
title_fullStr MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
title_full_unstemmed MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
title_short MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome
title_sort mog antibody seropositivity in a patient with encephalitis beyond the classical syndrome
topic Autoimmune diseases
Encephalitis
Anti-myelin oligodendrocyte glycoprotein antibodies (MOG-abs)
url http://link.springer.com/article/10.1186/s12883-017-0971-6
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