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Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report
BACKGROUND: Reversible posterior leukoencephalopathy syndrome (RPLS) is a rare and heterogeneous clinico-neuroradiological syndrome characterized by headache, altered mental status, seizures, and visual disturbances. Hypertension and immunosuppression are two of the main factors that predispose an i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495857/ https://www.ncbi.nlm.nih.gov/pubmed/32943018 http://dx.doi.org/10.1186/s12883-020-01922-x |
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author | Li, Kuan-Ying Chien, Ching-Fang Tsai, Chin-Ling Chen, Huang-Chi Wu, Meng-Ni Lai, Chiou-Lian Liou, Li-Min |
author_facet | Li, Kuan-Ying Chien, Ching-Fang Tsai, Chin-Ling Chen, Huang-Chi Wu, Meng-Ni Lai, Chiou-Lian Liou, Li-Min |
author_sort | Li, Kuan-Ying |
collection | PubMed |
description | BACKGROUND: Reversible posterior leukoencephalopathy syndrome (RPLS) is a rare and heterogeneous clinico-neuroradiological syndrome characterized by headache, altered mental status, seizures, and visual disturbances. Hypertension and immunosuppression are two of the main factors that predispose an individual to RPLS. However, RPLS can develop when no major risk factors are present. RPLS has been reported in pediatric nephrotic patients, but rarely in adults. CASE PRESENTATION: A 42-year-old Asian woman with nephrotic syndrome presented with seizures, headaches, and nausea. Her blood pressure was controlled, and no immunosuppressants had been prescribed. All symptoms and tests indicated RPLS following infection with pneumonia, which was successfully treated by immediate administration antibiotic and anti-epileptic medications. Seizures did not recur during a 2-year follow-up period. CONCLUSIONS: When patients with nephrotic syndrome have an infection, RPLS symptoms should be investigated thoroughly. With early diagnosis and appropriate treatment of RPLS, morbidity and mortality can be prevented. |
format | Online Article Text |
id | pubmed-7495857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74958572020-09-23 Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report Li, Kuan-Ying Chien, Ching-Fang Tsai, Chin-Ling Chen, Huang-Chi Wu, Meng-Ni Lai, Chiou-Lian Liou, Li-Min BMC Neurol Case Report BACKGROUND: Reversible posterior leukoencephalopathy syndrome (RPLS) is a rare and heterogeneous clinico-neuroradiological syndrome characterized by headache, altered mental status, seizures, and visual disturbances. Hypertension and immunosuppression are two of the main factors that predispose an individual to RPLS. However, RPLS can develop when no major risk factors are present. RPLS has been reported in pediatric nephrotic patients, but rarely in adults. CASE PRESENTATION: A 42-year-old Asian woman with nephrotic syndrome presented with seizures, headaches, and nausea. Her blood pressure was controlled, and no immunosuppressants had been prescribed. All symptoms and tests indicated RPLS following infection with pneumonia, which was successfully treated by immediate administration antibiotic and anti-epileptic medications. Seizures did not recur during a 2-year follow-up period. CONCLUSIONS: When patients with nephrotic syndrome have an infection, RPLS symptoms should be investigated thoroughly. With early diagnosis and appropriate treatment of RPLS, morbidity and mortality can be prevented. BioMed Central 2020-09-17 /pmc/articles/PMC7495857/ /pubmed/32943018 http://dx.doi.org/10.1186/s12883-020-01922-x 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 Li, Kuan-Ying Chien, Ching-Fang Tsai, Chin-Ling Chen, Huang-Chi Wu, Meng-Ni Lai, Chiou-Lian Liou, Li-Min Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title | Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title_full | Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title_fullStr | Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title_full_unstemmed | Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title_short | Infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
title_sort | infection-provoked reversible posterior leukoencephalopathy syndrome in an adult with nephrotic syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495857/ https://www.ncbi.nlm.nih.gov/pubmed/32943018 http://dx.doi.org/10.1186/s12883-020-01922-x |
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