Cargando…

Atypical presentation of an atypical pneumonia: a case report

BACKGROUND: Neurologic impediments occur in only 0.1% of Mycoplasma pneumoniae infections. Although direct intracerebral infection can occur in these patients, autoimmune-mediated reactions secondary to molecular mimicry are the most common pathophysiology of such neurological complications. These c...

Descripción completa

Detalles Bibliográficos
Autores principales: Payus, Alvin Oliver, Clarence, Clarita, Nee, Tiong, Yahya, Wan Nur Nafisah Wan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925204/
https://www.ncbi.nlm.nih.gov/pubmed/35292096
http://dx.doi.org/10.1186/s13256-022-03320-y
_version_ 1784670020062674944
author Payus, Alvin Oliver
Clarence, Clarita
Nee, Tiong
Yahya, Wan Nur Nafisah Wan
author_facet Payus, Alvin Oliver
Clarence, Clarita
Nee, Tiong
Yahya, Wan Nur Nafisah Wan
author_sort Payus, Alvin Oliver
collection PubMed
description BACKGROUND: Neurologic impediments occur in only 0.1% of Mycoplasma pneumoniae infections. Although direct intracerebral infection can occur in these patients, autoimmune-mediated reactions secondary to molecular mimicry are the most common pathophysiology of such neurological complications. These complications include immune-mediated encephalitis, peripheral neuritis such as Guillain–Barré syndrome, and many others. Miller Fisher syndrome is a one of the variants of Guillain–Barré syndrome that has been rarely linked to Mycoplasma pneumoniae infection. It is a condition classically characterized by the triad of ophthalmoplegia, areflexia, and ataxia. Most patients with Miller Fisher syndrome will have positive anti-ganglioside GQ1b antibodies found in their serum, making this autoantibody a very useful serological confirmation parameter. We report a case of a Miller Fisher syndrome in a woman with Mycoplasma pneumoniae infection. To the best of the authors’ knowledge, such cases have been only rarely described in literature. CASE PRESENTATION: A 35-year-old Chinese woman presented with sudden onset of double vision and ataxia 5 days after fever and mild flu symptoms. Her Mycoplasma pneumoniae antigen was positive with 1 over 2560 titer of total mycoplasma antibody and presence of immunoglobulin M antibody, suggesting acute infection, and her nerve conduction study revealed mild sensory axonal polyneuropathy with segmental demyelination. the Miller Fischer syndrome variant of Guillain-Barré syndrome secondary to Mycoplasma pneumonia was suspected and later confirmed by presence of serum anti-GQ1b autoantibody. She was treated with intravenous immunoglobulin 0.4 g/kg once daily for 5 days. CONCLUSIONS: The objective of this report is to share a case of an uncommon neurological complication of Mycoplasma pneumoniae infection, to increase the level of suspicion among clinicians that Miller Fischer syndrome can occur as an atypical presentation of an atypical pneumonia.
format Online
Article
Text
id pubmed-8925204
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-89252042022-03-23 Atypical presentation of an atypical pneumonia: a case report Payus, Alvin Oliver Clarence, Clarita Nee, Tiong Yahya, Wan Nur Nafisah Wan J Med Case Rep Case Report BACKGROUND: Neurologic impediments occur in only 0.1% of Mycoplasma pneumoniae infections. Although direct intracerebral infection can occur in these patients, autoimmune-mediated reactions secondary to molecular mimicry are the most common pathophysiology of such neurological complications. These complications include immune-mediated encephalitis, peripheral neuritis such as Guillain–Barré syndrome, and many others. Miller Fisher syndrome is a one of the variants of Guillain–Barré syndrome that has been rarely linked to Mycoplasma pneumoniae infection. It is a condition classically characterized by the triad of ophthalmoplegia, areflexia, and ataxia. Most patients with Miller Fisher syndrome will have positive anti-ganglioside GQ1b antibodies found in their serum, making this autoantibody a very useful serological confirmation parameter. We report a case of a Miller Fisher syndrome in a woman with Mycoplasma pneumoniae infection. To the best of the authors’ knowledge, such cases have been only rarely described in literature. CASE PRESENTATION: A 35-year-old Chinese woman presented with sudden onset of double vision and ataxia 5 days after fever and mild flu symptoms. Her Mycoplasma pneumoniae antigen was positive with 1 over 2560 titer of total mycoplasma antibody and presence of immunoglobulin M antibody, suggesting acute infection, and her nerve conduction study revealed mild sensory axonal polyneuropathy with segmental demyelination. the Miller Fischer syndrome variant of Guillain-Barré syndrome secondary to Mycoplasma pneumonia was suspected and later confirmed by presence of serum anti-GQ1b autoantibody. She was treated with intravenous immunoglobulin 0.4 g/kg once daily for 5 days. CONCLUSIONS: The objective of this report is to share a case of an uncommon neurological complication of Mycoplasma pneumoniae infection, to increase the level of suspicion among clinicians that Miller Fischer syndrome can occur as an atypical presentation of an atypical pneumonia. BioMed Central 2022-03-16 /pmc/articles/PMC8925204/ /pubmed/35292096 http://dx.doi.org/10.1186/s13256-022-03320-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Payus, Alvin Oliver
Clarence, Clarita
Nee, Tiong
Yahya, Wan Nur Nafisah Wan
Atypical presentation of an atypical pneumonia: a case report
title Atypical presentation of an atypical pneumonia: a case report
title_full Atypical presentation of an atypical pneumonia: a case report
title_fullStr Atypical presentation of an atypical pneumonia: a case report
title_full_unstemmed Atypical presentation of an atypical pneumonia: a case report
title_short Atypical presentation of an atypical pneumonia: a case report
title_sort atypical presentation of an atypical pneumonia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925204/
https://www.ncbi.nlm.nih.gov/pubmed/35292096
http://dx.doi.org/10.1186/s13256-022-03320-y
work_keys_str_mv AT payusalvinoliver atypicalpresentationofanatypicalpneumoniaacasereport
AT clarenceclarita atypicalpresentationofanatypicalpneumoniaacasereport
AT neetiong atypicalpresentationofanatypicalpneumoniaacasereport
AT yahyawannurnafisahwan atypicalpresentationofanatypicalpneumoniaacasereport