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Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report
BACKGROUND: Neuroleptic malignant syndrome (NMS) is a rare and occasionally fatal undesirable reaction to dopamine antagonists, and its phenotype is diverse owing to causative drugs. Classically, elevation of serum creatine kinase is described in NMS. Some reports have described muscular pathologica...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617376/ https://www.ncbi.nlm.nih.gov/pubmed/36309650 http://dx.doi.org/10.1186/s12883-022-02937-2 |
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author | Kakinuma, Yuki Amano, Ryota Ishida, Atsushi Nishino, Ichizo Taki, Katsumi |
author_facet | Kakinuma, Yuki Amano, Ryota Ishida, Atsushi Nishino, Ichizo Taki, Katsumi |
author_sort | Kakinuma, Yuki |
collection | PubMed |
description | BACKGROUND: Neuroleptic malignant syndrome (NMS) is a rare and occasionally fatal undesirable reaction to dopamine antagonists, and its phenotype is diverse owing to causative drugs. Classically, elevation of serum creatine kinase is described in NMS. Some reports have described muscular pathological findings; however, muscle magnetic resonance imaging (MRI) has not been reported previously. CASE PRESENTATION: A 63-year-old woman with a history of schizophrenia presented to our hospital with a high fever, excessive sweating, muscle weakness, and elevated serum creatine kinase levels. Muscle MRI revealed T2 high-intensity lesions in several muscles with gadolinium enhancement, and the pathology of the muscle biopsy showed a very mild presence of muscle fiber necrosis and regeneration with type 2c fibers without inflammation. Her symptoms resolved by treatment with levodopa/carbidopa, dantrolene. Finally, the patient was diagnosed with NMS. CONCLUSIONS: This is the first report of muscle MRI abnormalities in a patient with NMS. Muscle MRI abnormalities in NMS may be associated with non-inflammatory myopathic changes. The cause of creatine kinase elevation cannot be explained by abnormal strong muscle contraction nor inflammation. |
format | Online Article Text |
id | pubmed-9617376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96173762022-10-30 Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report Kakinuma, Yuki Amano, Ryota Ishida, Atsushi Nishino, Ichizo Taki, Katsumi BMC Neurol Case Report BACKGROUND: Neuroleptic malignant syndrome (NMS) is a rare and occasionally fatal undesirable reaction to dopamine antagonists, and its phenotype is diverse owing to causative drugs. Classically, elevation of serum creatine kinase is described in NMS. Some reports have described muscular pathological findings; however, muscle magnetic resonance imaging (MRI) has not been reported previously. CASE PRESENTATION: A 63-year-old woman with a history of schizophrenia presented to our hospital with a high fever, excessive sweating, muscle weakness, and elevated serum creatine kinase levels. Muscle MRI revealed T2 high-intensity lesions in several muscles with gadolinium enhancement, and the pathology of the muscle biopsy showed a very mild presence of muscle fiber necrosis and regeneration with type 2c fibers without inflammation. Her symptoms resolved by treatment with levodopa/carbidopa, dantrolene. Finally, the patient was diagnosed with NMS. CONCLUSIONS: This is the first report of muscle MRI abnormalities in a patient with NMS. Muscle MRI abnormalities in NMS may be associated with non-inflammatory myopathic changes. The cause of creatine kinase elevation cannot be explained by abnormal strong muscle contraction nor inflammation. BioMed Central 2022-10-29 /pmc/articles/PMC9617376/ /pubmed/36309650 http://dx.doi.org/10.1186/s12883-022-02937-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Kakinuma, Yuki Amano, Ryota Ishida, Atsushi Nishino, Ichizo Taki, Katsumi Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title | Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title_full | Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title_fullStr | Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title_full_unstemmed | Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title_short | Muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
title_sort | muscle magnetic resonance imaging abnormality in neuroleptic malignant syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617376/ https://www.ncbi.nlm.nih.gov/pubmed/36309650 http://dx.doi.org/10.1186/s12883-022-02937-2 |
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