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T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?

Amyotrophic Lateral Sclerosis (ALS) is a rare, devastating motor neuron disease characterized by the degeneration of upper and lower motor neurons causing muscular weakness, paralysis, and eventual death. MRI plays a supportive role in the diagnosis; its primary role is to exclude other clinical mim...

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Autores principales: Pai, Vivek, Trivedi, Chintan R, Pai, Bhujang, Swaminathan, Saravana K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062945/
https://www.ncbi.nlm.nih.gov/pubmed/35510239
http://dx.doi.org/10.25259/JCIS_24_2022
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author Pai, Vivek
Trivedi, Chintan R
Pai, Bhujang
Swaminathan, Saravana K
author_facet Pai, Vivek
Trivedi, Chintan R
Pai, Bhujang
Swaminathan, Saravana K
author_sort Pai, Vivek
collection PubMed
description Amyotrophic Lateral Sclerosis (ALS) is a rare, devastating motor neuron disease characterized by the degeneration of upper and lower motor neurons causing muscular weakness, paralysis, and eventual death. MRI plays a supportive role in the diagnosis; its primary role is to exclude other clinical mimics. Some of the imaging features associated with ALS include hypointense signal along the motor cortices on susceptibility or T2*-weighted imaging and hyperintensity along the corticospinal tracts (CST) within the cerebral hemispheres, brainstem, and spinal cord on the T2 weighted imaging. In this report, we discuss the value of T1 hyperintensity along the CST, especially in the spinal cord.
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spelling pubmed-90629452022-05-03 T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis? Pai, Vivek Trivedi, Chintan R Pai, Bhujang Swaminathan, Saravana K J Clin Imaging Sci Case Report Amyotrophic Lateral Sclerosis (ALS) is a rare, devastating motor neuron disease characterized by the degeneration of upper and lower motor neurons causing muscular weakness, paralysis, and eventual death. MRI plays a supportive role in the diagnosis; its primary role is to exclude other clinical mimics. Some of the imaging features associated with ALS include hypointense signal along the motor cortices on susceptibility or T2*-weighted imaging and hyperintensity along the corticospinal tracts (CST) within the cerebral hemispheres, brainstem, and spinal cord on the T2 weighted imaging. In this report, we discuss the value of T1 hyperintensity along the CST, especially in the spinal cord. Scientific Scholar 2022-04-27 /pmc/articles/PMC9062945/ /pubmed/35510239 http://dx.doi.org/10.25259/JCIS_24_2022 Text en © 2022 Published by Scientific Scholar on behalf of Journal of Clinical Imaging Science https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Pai, Vivek
Trivedi, Chintan R
Pai, Bhujang
Swaminathan, Saravana K
T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title_full T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title_fullStr T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title_full_unstemmed T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title_short T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?
title_sort t1 hyperintensity in the spinal cord: a diagnostic marker of amyotrophic lateral sclerosis?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062945/
https://www.ncbi.nlm.nih.gov/pubmed/35510239
http://dx.doi.org/10.25259/JCIS_24_2022
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