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Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder
CONTEXT: Proximal lower limb weakness presenting acutely with or without preceding fever is a strong mimic of Guillain–Barré syndrome (GBS). Benign acute childhood myositis (BACM) forms an important differential diagnosis in such cases. AIM: To characterize the clinical and laboratory findings of pa...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413614/ https://www.ncbi.nlm.nih.gov/pubmed/30937080 http://dx.doi.org/10.4103/JPN.JPN_116_18 |
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author | Pradhan, Sunil Das, Animesh Anand, Sucharita |
author_facet | Pradhan, Sunil Das, Animesh Anand, Sucharita |
author_sort | Pradhan, Sunil |
collection | PubMed |
description | CONTEXT: Proximal lower limb weakness presenting acutely with or without preceding fever is a strong mimic of Guillain–Barré syndrome (GBS). Benign acute childhood myositis (BACM) forms an important differential diagnosis in such cases. AIM: To characterize the clinical and laboratory findings of patients with BACM for better understanding of the disease. SETTINGS AND DESIGN: This prospective longitudinal study was conducted in a tertiary care hospital of northern India. MATERIALS AND METHODS: Thirty-two patients presenting in the outpatient or emergency clinic of the hospital with severe myalgia that exacerbated with straight leg raising test and fever from July 2016 to July 2017 were included in the study. STATISTICAL ANALYSIS: All the continuous data were expressed as number and percentage or mean ± standard deviation/median. Non-parametric continuous data between groups were analyzed by Friedman’s test. RESULTS: The mean age of the patients was 14.3 (±8.7) years and they presented after a nonspecific febrile illness in most of the cases (53.1%). The symptoms resolved after a mean of 5.7 (±1.6) days. Myalgia was present in 21 (65%) cases, whereas proximal weakness was the prominent finding in 14 (43%) cases. Electrolyte abnormality (hypokalemia) was present in four (12.5%) cases. In all patients, the muscle enzymes (creatine phosphokinase, serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, and lactate dehydrogenase) were elevated at presentation, and electromyography showed myopathic pattern. A significant recovery took place in the next 5–7 days. CONCLUSION: BACM should be actively looked for in cases of painful acute proximal limb weakness in the adolescents. |
format | Online Article Text |
id | pubmed-6413614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64136142019-04-01 Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder Pradhan, Sunil Das, Animesh Anand, Sucharita J Pediatr Neurosci Original Article CONTEXT: Proximal lower limb weakness presenting acutely with or without preceding fever is a strong mimic of Guillain–Barré syndrome (GBS). Benign acute childhood myositis (BACM) forms an important differential diagnosis in such cases. AIM: To characterize the clinical and laboratory findings of patients with BACM for better understanding of the disease. SETTINGS AND DESIGN: This prospective longitudinal study was conducted in a tertiary care hospital of northern India. MATERIALS AND METHODS: Thirty-two patients presenting in the outpatient or emergency clinic of the hospital with severe myalgia that exacerbated with straight leg raising test and fever from July 2016 to July 2017 were included in the study. STATISTICAL ANALYSIS: All the continuous data were expressed as number and percentage or mean ± standard deviation/median. Non-parametric continuous data between groups were analyzed by Friedman’s test. RESULTS: The mean age of the patients was 14.3 (±8.7) years and they presented after a nonspecific febrile illness in most of the cases (53.1%). The symptoms resolved after a mean of 5.7 (±1.6) days. Myalgia was present in 21 (65%) cases, whereas proximal weakness was the prominent finding in 14 (43%) cases. Electrolyte abnormality (hypokalemia) was present in four (12.5%) cases. In all patients, the muscle enzymes (creatine phosphokinase, serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, and lactate dehydrogenase) were elevated at presentation, and electromyography showed myopathic pattern. A significant recovery took place in the next 5–7 days. CONCLUSION: BACM should be actively looked for in cases of painful acute proximal limb weakness in the adolescents. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6413614/ /pubmed/30937080 http://dx.doi.org/10.4103/JPN.JPN_116_18 Text en Copyright: © 2019 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Pradhan, Sunil Das, Animesh Anand, Sucharita Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title | Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title_full | Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title_fullStr | Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title_full_unstemmed | Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title_short | Benign Acute Childhood Myositis: A Benign Disease that Mimics More Severe Neuromuscular Disorder |
title_sort | benign acute childhood myositis: a benign disease that mimics more severe neuromuscular disorder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413614/ https://www.ncbi.nlm.nih.gov/pubmed/30937080 http://dx.doi.org/10.4103/JPN.JPN_116_18 |
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