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Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature

INTRODUCTION: Neuromyelitis optica is a demyelinating disease of the central nervous system that predominantly affects the optic nerves and spinal cord. In neuromyelitis optica, white blood cells and antibodies primarily attack the optic nerves and the spinal cord, but may also attack the brain. Bra...

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Autores principales: Kassu, Rodas Asrat, Mulatu, Hailu Abera, Gizaw, Sisay, Fisseha, Henok, Musema, Amir, Keder, Ayube, Negash, Semere, Tefera, Fithanegest, Lissanwerk, Adugna, Tamrat, Lemlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485543/
https://www.ncbi.nlm.nih.gov/pubmed/34598735
http://dx.doi.org/10.1186/s13256-021-03019-6
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author Kassu, Rodas Asrat
Mulatu, Hailu Abera
Gizaw, Sisay
Fisseha, Henok
Musema, Amir
Keder, Ayube
Negash, Semere
Tefera, Fithanegest
Lissanwerk, Adugna
Tamrat, Lemlem
author_facet Kassu, Rodas Asrat
Mulatu, Hailu Abera
Gizaw, Sisay
Fisseha, Henok
Musema, Amir
Keder, Ayube
Negash, Semere
Tefera, Fithanegest
Lissanwerk, Adugna
Tamrat, Lemlem
author_sort Kassu, Rodas Asrat
collection PubMed
description INTRODUCTION: Neuromyelitis optica is a demyelinating disease of the central nervous system that predominantly affects the optic nerves and spinal cord. In neuromyelitis optica, white blood cells and antibodies primarily attack the optic nerves and the spinal cord, but may also attack the brain. Brainstem manifestation has been described recently. So far, neuromyelitis optica is very rare in Ethiopia and there were only two case reports, but this is the first case report of neuromyelitis optica with brainstem involvement. CASE PRESENTATION: A 47-year-old Addis Ababa woman presented to Saint Paul’s Hospital Millennium Medical College with a history of visual loss of 7 years and bilateral lower limb weakness of 4 days duration. She had bilateral oculomotor nerve palsy. Her past medical history showed systemic hypertension for 18 years and dyslipidemia for 1 year. The objective evaluation of the patient revealed right optic nerve atrophy suggesting optic neuritis and flaccid paraplegia with sensory level at the fourth thoracic vertebra. Diagnostic work-up using electromyography and spinal magnetic resonance imaging revealed demyelinating anterior visual pathway dysfunction and signs of extensive cervicothoracic transverse myelitis from the third cervical to lower thoracic vertebrae, respectively. Then a diagnosis of neuromyelitis optica was established. After treatment with high-dose systemic steroid followed by azathioprine, the patient was stable for several months with significant improvement of vision and lower-extremity weakness with no relapse of symptoms. CONCLUSION: The case described here is a rare inflammatory demyelinating disorder of the central nervous system occurring in East Africa. It reminds clinicians to suspect neuromyelitis optica in a patient who presented with unexplained recurrent optic neuritis to make a timely diagnosis and prevention of permanent neuronal damage. Neuromyelitis optica can also be associated with oculomotor nerve involvement.
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spelling pubmed-84855432021-10-04 Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature Kassu, Rodas Asrat Mulatu, Hailu Abera Gizaw, Sisay Fisseha, Henok Musema, Amir Keder, Ayube Negash, Semere Tefera, Fithanegest Lissanwerk, Adugna Tamrat, Lemlem J Med Case Rep Case Report INTRODUCTION: Neuromyelitis optica is a demyelinating disease of the central nervous system that predominantly affects the optic nerves and spinal cord. In neuromyelitis optica, white blood cells and antibodies primarily attack the optic nerves and the spinal cord, but may also attack the brain. Brainstem manifestation has been described recently. So far, neuromyelitis optica is very rare in Ethiopia and there were only two case reports, but this is the first case report of neuromyelitis optica with brainstem involvement. CASE PRESENTATION: A 47-year-old Addis Ababa woman presented to Saint Paul’s Hospital Millennium Medical College with a history of visual loss of 7 years and bilateral lower limb weakness of 4 days duration. She had bilateral oculomotor nerve palsy. Her past medical history showed systemic hypertension for 18 years and dyslipidemia for 1 year. The objective evaluation of the patient revealed right optic nerve atrophy suggesting optic neuritis and flaccid paraplegia with sensory level at the fourth thoracic vertebra. Diagnostic work-up using electromyography and spinal magnetic resonance imaging revealed demyelinating anterior visual pathway dysfunction and signs of extensive cervicothoracic transverse myelitis from the third cervical to lower thoracic vertebrae, respectively. Then a diagnosis of neuromyelitis optica was established. After treatment with high-dose systemic steroid followed by azathioprine, the patient was stable for several months with significant improvement of vision and lower-extremity weakness with no relapse of symptoms. CONCLUSION: The case described here is a rare inflammatory demyelinating disorder of the central nervous system occurring in East Africa. It reminds clinicians to suspect neuromyelitis optica in a patient who presented with unexplained recurrent optic neuritis to make a timely diagnosis and prevention of permanent neuronal damage. Neuromyelitis optica can also be associated with oculomotor nerve involvement. BioMed Central 2021-10-01 /pmc/articles/PMC8485543/ /pubmed/34598735 http://dx.doi.org/10.1186/s13256-021-03019-6 Text en © The Author(s) 2021 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
Kassu, Rodas Asrat
Mulatu, Hailu Abera
Gizaw, Sisay
Fisseha, Henok
Musema, Amir
Keder, Ayube
Negash, Semere
Tefera, Fithanegest
Lissanwerk, Adugna
Tamrat, Lemlem
Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title_full Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title_fullStr Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title_full_unstemmed Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title_short Neuromyelitis optica with brain stem involvement in a middle-aged Ethiopian woman: a case report and review of literature
title_sort neuromyelitis optica with brain stem involvement in a middle-aged ethiopian woman: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485543/
https://www.ncbi.nlm.nih.gov/pubmed/34598735
http://dx.doi.org/10.1186/s13256-021-03019-6
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