Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices

Pediatric multiple sclerosis (MS) represents less than 5% of the MS population, but patients with pediatric-onset disease reach permanent disability at a younger age than adult onset patients. Accurate diagnosis at presentation and optimal long-term treatment is vital to mitigate ongoing neuroinflam...

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Main Authors: Chou, I-Jun, Wang, Huei-Shyong, Whitehouse, William P., Constantinescu, Cris S.
Format: Article
Published: Springer 2016
Subjects:
Online Access:https://eprints.nottingham.ac.uk/33485/
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author Chou, I-Jun
Wang, Huei-Shyong
Whitehouse, William P.
Constantinescu, Cris S.
author_facet Chou, I-Jun
Wang, Huei-Shyong
Whitehouse, William P.
Constantinescu, Cris S.
author_sort Chou, I-Jun
building Nottingham Research Data Repository
collection Online Access
description Pediatric multiple sclerosis (MS) represents less than 5% of the MS population, but patients with pediatric-onset disease reach permanent disability at a younger age than adult onset patients. Accurate diagnosis at presentation and optimal long-term treatment is vital to mitigate ongoing neuroinflammation and irreversible neurodegeneration.
However, it may be difficult to early differentiate pediatric MS from acute disseminated
encephalomyelitis (ADEM) and neuromyelitis optica spectrum disorders (NMOSD) as they often have atypical presentation that differs from that of adult-onset MS. The
purpose of this review is to summarize the updated views on diagnostic criteria, imaging, histopathology and treatment choices.
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spelling nottingham-334852020-05-04T17:57:32Z https://eprints.nottingham.ac.uk/33485/ Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices Chou, I-Jun Wang, Huei-Shyong Whitehouse, William P. Constantinescu, Cris S. Pediatric multiple sclerosis (MS) represents less than 5% of the MS population, but patients with pediatric-onset disease reach permanent disability at a younger age than adult onset patients. Accurate diagnosis at presentation and optimal long-term treatment is vital to mitigate ongoing neuroinflammation and irreversible neurodegeneration.
However, it may be difficult to early differentiate pediatric MS from acute disseminated
encephalomyelitis (ADEM) and neuromyelitis optica spectrum disorders (NMOSD) as they often have atypical presentation that differs from that of adult-onset MS. The
purpose of this review is to summarize the updated views on diagnostic criteria, imaging, histopathology and treatment choices. Springer 2016-06-06 Article PeerReviewed Chou, I-Jun, Wang, Huei-Shyong, Whitehouse, William P. and Constantinescu, Cris S. (2016) Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices. Current Neurology and Neuroscience Reports, 16 (7). pp. 1-12. ISSN 1534-6293 ADEM; CIS; Demyelination; MRI; NMOSD http://link.springer.com/article/10.1007%2Fs11910-016-0663-4 doi:10.1007/s11910-016-0663-4 doi:10.1007/s11910-016-0663-4
spellingShingle ADEM; CIS; Demyelination; MRI; NMOSD
Chou, I-Jun
Wang, Huei-Shyong
Whitehouse, William P.
Constantinescu, Cris S.
Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title_full Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title_fullStr Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title_full_unstemmed Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title_short Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
title_sort pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices
topic ADEM; CIS; Demyelination; MRI; NMOSD
url https://eprints.nottingham.ac.uk/33485/
https://eprints.nottingham.ac.uk/33485/
https://eprints.nottingham.ac.uk/33485/