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Four cases of pediatric neuralgic amyotrophy treated with immunotherapy: one-year follow-up and literature review
Neuralgic amyotrophy (NA) is a neurological disease that occurs across all age groups, but its prognosis in children is controversial. The present report adds to the knowledge about its prognosis by describing four cases of pediatric NA in which the patients were treated with immunotherapy and follo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132571/ https://www.ncbi.nlm.nih.gov/pubmed/32228355 http://dx.doi.org/10.1177/0300060520912082 |
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author | Hu, Xiaoyue Jing, Miao Feng, Jun Tang, Jihong |
author_facet | Hu, Xiaoyue Jing, Miao Feng, Jun Tang, Jihong |
author_sort | Hu, Xiaoyue |
collection | PubMed |
description | Neuralgic amyotrophy (NA) is a neurological disease that occurs across all age groups, but its prognosis in children is controversial. The present report adds to the knowledge about its prognosis by describing four cases of pediatric NA in which the patients were treated with immunotherapy and followed up for 1 year. We also present a summary of relevant cases of pediatric NA treated with immunotherapy. The clinical features of the four present cases were similar to those of previously reported cases, and their symptoms improved after immunotherapy. At the 1-year follow-up, three of the children gained near complete recovery, and their improvement was significantly better than that observed at the 2-month follow-up. A review of the literature showed that most previously reported children with NA showed improvement after immunotherapy, but no more than half of the patients recovered fully. These findings indicate that in children with NA, immunotherapy is fairly effective and its benefits improve with time. Thus, long-term follow-up is needed in these patients to determine their prognosis. |
format | Online Article Text |
id | pubmed-7132571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71325712020-04-13 Four cases of pediatric neuralgic amyotrophy treated with immunotherapy: one-year follow-up and literature review Hu, Xiaoyue Jing, Miao Feng, Jun Tang, Jihong J Int Med Res Case Report Neuralgic amyotrophy (NA) is a neurological disease that occurs across all age groups, but its prognosis in children is controversial. The present report adds to the knowledge about its prognosis by describing four cases of pediatric NA in which the patients were treated with immunotherapy and followed up for 1 year. We also present a summary of relevant cases of pediatric NA treated with immunotherapy. The clinical features of the four present cases were similar to those of previously reported cases, and their symptoms improved after immunotherapy. At the 1-year follow-up, three of the children gained near complete recovery, and their improvement was significantly better than that observed at the 2-month follow-up. A review of the literature showed that most previously reported children with NA showed improvement after immunotherapy, but no more than half of the patients recovered fully. These findings indicate that in children with NA, immunotherapy is fairly effective and its benefits improve with time. Thus, long-term follow-up is needed in these patients to determine their prognosis. SAGE Publications 2020-03-31 /pmc/articles/PMC7132571/ /pubmed/32228355 http://dx.doi.org/10.1177/0300060520912082 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Hu, Xiaoyue Jing, Miao Feng, Jun Tang, Jihong Four cases of pediatric neuralgic amyotrophy treated with immunotherapy: one-year follow-up and literature review |
title | Four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
title_full | Four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
title_fullStr | Four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
title_full_unstemmed | Four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
title_short | Four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
title_sort | four cases of pediatric neuralgic amyotrophy treated with
immunotherapy: one-year follow-up and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132571/ https://www.ncbi.nlm.nih.gov/pubmed/32228355 http://dx.doi.org/10.1177/0300060520912082 |
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