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Pediatric immune-mediated necrotizing myopathy

Immune-mediated necrotizing myopathy (IMNM) is a type of inflammatory myopathy. Most patients with IMNM produce anti-3-hydroxy-3-methylglutaryl coenzyme A reductase or anti-signal-recognition particle autoantibodies. IMNM is much rarer in children than in adults. We conducted this mini review focusi...

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Detalles Bibliográficos
Autores principales: Wang, Chen-Hua, Liang, Wen-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067916/
https://www.ncbi.nlm.nih.gov/pubmed/37021281
http://dx.doi.org/10.3389/fneur.2023.1123380
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author Wang, Chen-Hua
Liang, Wen-Chen
author_facet Wang, Chen-Hua
Liang, Wen-Chen
author_sort Wang, Chen-Hua
collection PubMed
description Immune-mediated necrotizing myopathy (IMNM) is a type of inflammatory myopathy. Most patients with IMNM produce anti-3-hydroxy-3-methylglutaryl coenzyme A reductase or anti-signal-recognition particle autoantibodies. IMNM is much rarer in children than in adults. We conducted this mini review focusing on pediatric IMNM to present current evidence regarding its epidemiology, clinical characteristics, diagnosis, and treatment. Our findings indicate that pediatric IMNM often causes severe muscle weakness and is refractory to corticosteroids alone. Furthermore, delayed diagnosis is common because of the clinicopathological similarity between IMNM and inherited myopathy. Raising awareness regarding pediatric IMNM may facilitate early diagnosis and effective treatment.
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spelling pubmed-100679162023-04-04 Pediatric immune-mediated necrotizing myopathy Wang, Chen-Hua Liang, Wen-Chen Front Neurol Neurology Immune-mediated necrotizing myopathy (IMNM) is a type of inflammatory myopathy. Most patients with IMNM produce anti-3-hydroxy-3-methylglutaryl coenzyme A reductase or anti-signal-recognition particle autoantibodies. IMNM is much rarer in children than in adults. We conducted this mini review focusing on pediatric IMNM to present current evidence regarding its epidemiology, clinical characteristics, diagnosis, and treatment. Our findings indicate that pediatric IMNM often causes severe muscle weakness and is refractory to corticosteroids alone. Furthermore, delayed diagnosis is common because of the clinicopathological similarity between IMNM and inherited myopathy. Raising awareness regarding pediatric IMNM may facilitate early diagnosis and effective treatment. Frontiers Media S.A. 2023-03-20 /pmc/articles/PMC10067916/ /pubmed/37021281 http://dx.doi.org/10.3389/fneur.2023.1123380 Text en Copyright © 2023 Wang and Liang. https://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) and the copyright owner(s) 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 Neurology
Wang, Chen-Hua
Liang, Wen-Chen
Pediatric immune-mediated necrotizing myopathy
title Pediatric immune-mediated necrotizing myopathy
title_full Pediatric immune-mediated necrotizing myopathy
title_fullStr Pediatric immune-mediated necrotizing myopathy
title_full_unstemmed Pediatric immune-mediated necrotizing myopathy
title_short Pediatric immune-mediated necrotizing myopathy
title_sort pediatric immune-mediated necrotizing myopathy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067916/
https://www.ncbi.nlm.nih.gov/pubmed/37021281
http://dx.doi.org/10.3389/fneur.2023.1123380
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