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Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course
OBJECTIVE: The main objective of this study was to evaluate the correlation between the distribution of brachial plexus magnetic resonance imaging (MRI) abnormalities and clinical weakness, and to evaluate the value of brachial plexus MRI in predicting disease course and response to treatment in mul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434176/ https://www.ncbi.nlm.nih.gov/pubmed/28523213 http://dx.doi.org/10.1002/brb3.632 |
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author | Jongbloed, Bas A. Bos, Jeroen W. Rutgers, Dirk van der Pol, Willem Ludo van den Berg, Leonard H. |
author_facet | Jongbloed, Bas A. Bos, Jeroen W. Rutgers, Dirk van der Pol, Willem Ludo van den Berg, Leonard H. |
author_sort | Jongbloed, Bas A. |
collection | PubMed |
description | OBJECTIVE: The main objective of this study was to evaluate the correlation between the distribution of brachial plexus magnetic resonance imaging (MRI) abnormalities and clinical weakness, and to evaluate the value of brachial plexus MRI in predicting disease course and response to treatment in multifocal motor neuropathy (MMN), Lewis‐Sumner syndrome (LSS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). METHODS: Sixty‐seven patients with an inflammatory neuropathy diagnosed at our tertiary referral center for neuromuscular diseases had undergone bilateral T2‐weighted short tau inversion recovery (STIR) MRI of the brachial plexus. We obtained clinical follow‐up data and scored all MRIs for abnormalities and the symmetry of their distribution. RESULTS: Brachial plexus MRI abnormalities were detected in 45% of the patients. An abnormal MRI did not predict disease course in terms of patterns of weakness, sensory disturbances or response to treatment. Within the spectrum of radiological abnormalities, asymmetrical clinical syndromes, MMN and LSS were significantly associated with asymmetrical radiological abnormalities, whereas symmetrical abnormalities predominated in CIDP (p < .001, phi 0.791). CONCLUSION: T2 STIR brachial plexus MRI abnormalities correspond with the distribution of neurological deficits in inflammatory neuropathies, but do not correlate with specific clinical characteristics, response to treatment or disease course. |
format | Online Article Text |
id | pubmed-5434176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54341762017-05-18 Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course Jongbloed, Bas A. Bos, Jeroen W. Rutgers, Dirk van der Pol, Willem Ludo van den Berg, Leonard H. Brain Behav Original Research OBJECTIVE: The main objective of this study was to evaluate the correlation between the distribution of brachial plexus magnetic resonance imaging (MRI) abnormalities and clinical weakness, and to evaluate the value of brachial plexus MRI in predicting disease course and response to treatment in multifocal motor neuropathy (MMN), Lewis‐Sumner syndrome (LSS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). METHODS: Sixty‐seven patients with an inflammatory neuropathy diagnosed at our tertiary referral center for neuromuscular diseases had undergone bilateral T2‐weighted short tau inversion recovery (STIR) MRI of the brachial plexus. We obtained clinical follow‐up data and scored all MRIs for abnormalities and the symmetry of their distribution. RESULTS: Brachial plexus MRI abnormalities were detected in 45% of the patients. An abnormal MRI did not predict disease course in terms of patterns of weakness, sensory disturbances or response to treatment. Within the spectrum of radiological abnormalities, asymmetrical clinical syndromes, MMN and LSS were significantly associated with asymmetrical radiological abnormalities, whereas symmetrical abnormalities predominated in CIDP (p < .001, phi 0.791). CONCLUSION: T2 STIR brachial plexus MRI abnormalities correspond with the distribution of neurological deficits in inflammatory neuropathies, but do not correlate with specific clinical characteristics, response to treatment or disease course. John Wiley and Sons Inc. 2017-04-04 /pmc/articles/PMC5434176/ /pubmed/28523213 http://dx.doi.org/10.1002/brb3.632 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Jongbloed, Bas A. Bos, Jeroen W. Rutgers, Dirk van der Pol, Willem Ludo van den Berg, Leonard H. Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title | Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title_full | Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title_fullStr | Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title_full_unstemmed | Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title_short | Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
title_sort | brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434176/ https://www.ncbi.nlm.nih.gov/pubmed/28523213 http://dx.doi.org/10.1002/brb3.632 |
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