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Atypical spinal cord infarction: A case report
INTRODUCTION: The abrupt onset of sensorimotor deficits is a neurologic emergency that requires immediate management. Acute spontaneous spinal cord infarction (SCI) is rare, but can cause the sudden onset of quadriplegia or quadriparesis. Magnetic resonance imaging (MRI) is an essential imaging moda...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999478/ https://www.ncbi.nlm.nih.gov/pubmed/29879075 http://dx.doi.org/10.1097/MD.0000000000011058 |
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author | Ota, Koshi Iida, Ryo Ota, Kanna Sakaue, Masahide Takashima, Shogo Taniguchi, Kohei Tomioka, Masao Nitta, Masahiko Takasu, Akira |
author_facet | Ota, Koshi Iida, Ryo Ota, Kanna Sakaue, Masahide Takashima, Shogo Taniguchi, Kohei Tomioka, Masao Nitta, Masahiko Takasu, Akira |
author_sort | Ota, Koshi |
collection | PubMed |
description | INTRODUCTION: The abrupt onset of sensorimotor deficits is a neurologic emergency that requires immediate management. Acute spontaneous spinal cord infarction (SCI) is rare, but can cause the sudden onset of quadriplegia or quadriparesis. Magnetic resonance imaging (MRI) is an essential imaging modality to diagnose SCI. CASE PRESENTATION: A 75-year-old man with a history of diabetes mellitus type 2, hypertension, and dyslipidemia was transferred to our facility for further workup of the sudden onset of quadriplegia. Diffusion-weighted contrast MRI (DWI) on hospital day 8 revealed hyperintense signals predominantly at the grey matter, and a contrast T2 signal abnormality with a decreased apparent diffusion coefficient (ADC). Steroid pulse therapy was initiated because myelitis could not be completely ruled out, but this did not improve the neurological deficits. Spontaneous SCI was finally diagnosed as an exclusion diagnosis. Symptoms were gradually recovered with rehabilitation, and he was transferred to a rehabilitation facility on hospital day 40. CONCLUSION: MRI with DWI of the spine should be considered for an early diagnosis of SCI. A combination of DWI with ADC maps is recommended to distinguish SCI from other differential disorders. |
format | Online Article Text |
id | pubmed-5999478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-59994782018-06-20 Atypical spinal cord infarction: A case report Ota, Koshi Iida, Ryo Ota, Kanna Sakaue, Masahide Takashima, Shogo Taniguchi, Kohei Tomioka, Masao Nitta, Masahiko Takasu, Akira Medicine (Baltimore) Research Article INTRODUCTION: The abrupt onset of sensorimotor deficits is a neurologic emergency that requires immediate management. Acute spontaneous spinal cord infarction (SCI) is rare, but can cause the sudden onset of quadriplegia or quadriparesis. Magnetic resonance imaging (MRI) is an essential imaging modality to diagnose SCI. CASE PRESENTATION: A 75-year-old man with a history of diabetes mellitus type 2, hypertension, and dyslipidemia was transferred to our facility for further workup of the sudden onset of quadriplegia. Diffusion-weighted contrast MRI (DWI) on hospital day 8 revealed hyperintense signals predominantly at the grey matter, and a contrast T2 signal abnormality with a decreased apparent diffusion coefficient (ADC). Steroid pulse therapy was initiated because myelitis could not be completely ruled out, but this did not improve the neurological deficits. Spontaneous SCI was finally diagnosed as an exclusion diagnosis. Symptoms were gradually recovered with rehabilitation, and he was transferred to a rehabilitation facility on hospital day 40. CONCLUSION: MRI with DWI of the spine should be considered for an early diagnosis of SCI. A combination of DWI with ADC maps is recommended to distinguish SCI from other differential disorders. Wolters Kluwer Health 2018-06-18 /pmc/articles/PMC5999478/ /pubmed/29879075 http://dx.doi.org/10.1097/MD.0000000000011058 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Ota, Koshi Iida, Ryo Ota, Kanna Sakaue, Masahide Takashima, Shogo Taniguchi, Kohei Tomioka, Masao Nitta, Masahiko Takasu, Akira Atypical spinal cord infarction: A case report |
title | Atypical spinal cord infarction: A case report |
title_full | Atypical spinal cord infarction: A case report |
title_fullStr | Atypical spinal cord infarction: A case report |
title_full_unstemmed | Atypical spinal cord infarction: A case report |
title_short | Atypical spinal cord infarction: A case report |
title_sort | atypical spinal cord infarction: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999478/ https://www.ncbi.nlm.nih.gov/pubmed/29879075 http://dx.doi.org/10.1097/MD.0000000000011058 |
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