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Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature
BACKGROUND: Sjögren syndrome (SS) is a rare disease in pediatrics, and little attention has been paid to the clinical feature in these patients. To date, there are few cases concern about neurological and nephrological disorders in childhood Sjögren syndrome. We describe a case of Sjögren syndrome i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245745/ https://www.ncbi.nlm.nih.gov/pubmed/32448292 http://dx.doi.org/10.1186/s12969-020-00431-y |
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author | Zhao, Jingya Chen, Qin Zhu, Yunyun Zhao, Meng Liu, Jun Zhang, Zhenzhong Gong, Xiaoting |
author_facet | Zhao, Jingya Chen, Qin Zhu, Yunyun Zhao, Meng Liu, Jun Zhang, Zhenzhong Gong, Xiaoting |
author_sort | Zhao, Jingya |
collection | PubMed |
description | BACKGROUND: Sjögren syndrome (SS) is a rare disease in pediatrics, and little attention has been paid to the clinical feature in these patients. To date, there are few cases concern about neurological and nephrological disorders in childhood Sjögren syndrome. We describe a case of Sjögren syndrome in a 12-year-old girl who developed neurological disorders and interstitial nephritis and review the literature currently available on this topic. CASE PRESENTATION: A 12-year-old girl was admitted to our hospital for arthritis and glucosuria. She was required to do labial gland and renal biopsy, because the positive for anti-nuclear antibody and anti-Sjögren syndrome B (anti-SSB) antibody. Then the biopsy was performed revealing the lymphocytic infiltrate in the small area and renal tubular interstitial damage,thus the diagnosis of Sjögren syndrome with tubular interstitial damage was made. Three months later, she presented again with headache, fever, nausea, vomiting and was recovered without drug therapy. Based on the patient’s medical history, laboratory and imaging examination, and treatment, we speculate that the disorders of the nervous system were caused by the Sjögren syndrome. The girl has stable renal function and no residual nervous system damage in the next 1.5 years, but she underwent low dose prednisone therapy because of persistent renal glucosuria. CONCLUSIONS: Nephrological disorders and neurological involvement are rare manifestations of Sjögren syndrome in children, and rarely presented as the initial symptoms. It should be suspected in children presenting with unexplained renal diseases, neurological abnormalities, or unexplained fever. Although there is no guidelines on the diagnosis and treatment of children Sjögren syndrome are currently available, early recognition and the appropriate treatment of renal damage and neurologic involvement would improve prognosis and prevent complications. |
format | Online Article Text |
id | pubmed-7245745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72457452020-06-01 Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature Zhao, Jingya Chen, Qin Zhu, Yunyun Zhao, Meng Liu, Jun Zhang, Zhenzhong Gong, Xiaoting Pediatr Rheumatol Online J Case Report BACKGROUND: Sjögren syndrome (SS) is a rare disease in pediatrics, and little attention has been paid to the clinical feature in these patients. To date, there are few cases concern about neurological and nephrological disorders in childhood Sjögren syndrome. We describe a case of Sjögren syndrome in a 12-year-old girl who developed neurological disorders and interstitial nephritis and review the literature currently available on this topic. CASE PRESENTATION: A 12-year-old girl was admitted to our hospital for arthritis and glucosuria. She was required to do labial gland and renal biopsy, because the positive for anti-nuclear antibody and anti-Sjögren syndrome B (anti-SSB) antibody. Then the biopsy was performed revealing the lymphocytic infiltrate in the small area and renal tubular interstitial damage,thus the diagnosis of Sjögren syndrome with tubular interstitial damage was made. Three months later, she presented again with headache, fever, nausea, vomiting and was recovered without drug therapy. Based on the patient’s medical history, laboratory and imaging examination, and treatment, we speculate that the disorders of the nervous system were caused by the Sjögren syndrome. The girl has stable renal function and no residual nervous system damage in the next 1.5 years, but she underwent low dose prednisone therapy because of persistent renal glucosuria. CONCLUSIONS: Nephrological disorders and neurological involvement are rare manifestations of Sjögren syndrome in children, and rarely presented as the initial symptoms. It should be suspected in children presenting with unexplained renal diseases, neurological abnormalities, or unexplained fever. Although there is no guidelines on the diagnosis and treatment of children Sjögren syndrome are currently available, early recognition and the appropriate treatment of renal damage and neurologic involvement would improve prognosis and prevent complications. BioMed Central 2020-05-24 /pmc/articles/PMC7245745/ /pubmed/32448292 http://dx.doi.org/10.1186/s12969-020-00431-y Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Zhao, Jingya Chen, Qin Zhu, Yunyun Zhao, Meng Liu, Jun Zhang, Zhenzhong Gong, Xiaoting Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title | Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title_full | Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title_fullStr | Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title_full_unstemmed | Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title_short | Nephrological disorders and neurological involvement in pediatric primary Sjogren syndrome:a case report and review of literature |
title_sort | nephrological disorders and neurological involvement in pediatric primary sjogren syndrome:a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245745/ https://www.ncbi.nlm.nih.gov/pubmed/32448292 http://dx.doi.org/10.1186/s12969-020-00431-y |
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