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Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis

A 56-year-old woman with various neurological signs which developed over a 1-year period was admitted for evaluation. MRI showed a markedly abnormal signal in the cervical spine. Despite treatment with IV steroids, she developed a progressive myelopathy, became quadriplegic, and required intubation....

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Detalles Bibliográficos
Autores principales: Fisher, Arie, Rahman, Habib, Farrell, Michael, Hennessy, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742205/
https://www.ncbi.nlm.nih.gov/pubmed/29312127
http://dx.doi.org/10.3389/fneur.2017.00705
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author Fisher, Arie
Rahman, Habib
Farrell, Michael
Hennessy, Michael
author_facet Fisher, Arie
Rahman, Habib
Farrell, Michael
Hennessy, Michael
author_sort Fisher, Arie
collection PubMed
description A 56-year-old woman with various neurological signs which developed over a 1-year period was admitted for evaluation. MRI showed a markedly abnormal signal in the cervical spine. Despite treatment with IV steroids, she developed a progressive myelopathy, became quadriplegic, and required intubation. Immunomodulatory treatment was ineffective. The patient died 24 days after admission. Histopathological investigation revealed spinal cord necrosis with a lymphocyte predominant meningovascular inflammation involving arteries and veins along with evidence of prior occlusive disease of the anterior spinal artery. The changes were confined to the spinal cord. The present case represents an unusual cause of myelitis for which early and aggressive immunomodulatory treatment may have influenced outcomes.
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spelling pubmed-57422052018-01-08 Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis Fisher, Arie Rahman, Habib Farrell, Michael Hennessy, Michael Front Neurol Neuroscience A 56-year-old woman with various neurological signs which developed over a 1-year period was admitted for evaluation. MRI showed a markedly abnormal signal in the cervical spine. Despite treatment with IV steroids, she developed a progressive myelopathy, became quadriplegic, and required intubation. Immunomodulatory treatment was ineffective. The patient died 24 days after admission. Histopathological investigation revealed spinal cord necrosis with a lymphocyte predominant meningovascular inflammation involving arteries and veins along with evidence of prior occlusive disease of the anterior spinal artery. The changes were confined to the spinal cord. The present case represents an unusual cause of myelitis for which early and aggressive immunomodulatory treatment may have influenced outcomes. Frontiers Media S.A. 2017-12-19 /pmc/articles/PMC5742205/ /pubmed/29312127 http://dx.doi.org/10.3389/fneur.2017.00705 Text en Copyright © 2017 Fisher, Rahman, Farrell and Hennessy. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Fisher, Arie
Rahman, Habib
Farrell, Michael
Hennessy, Michael
Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title_full Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title_fullStr Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title_full_unstemmed Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title_short Progressive Fatal Myelopathy Secondary to Isolated Spinal Cord Vasculitis
title_sort progressive fatal myelopathy secondary to isolated spinal cord vasculitis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742205/
https://www.ncbi.nlm.nih.gov/pubmed/29312127
http://dx.doi.org/10.3389/fneur.2017.00705
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