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Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report

BACKGROUND: Posterior Reversible Encephalopathy Syndrome (PRES) is a neurotoxic state characterized by seizures, headache, vision change, paresis, and altered mental status. PRES has an important place in medicine due to the wide variety of causative diseases, infections, and medications that precip...

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Autores principales: Puram, Vikram V., Ghazaleh, Dana, Salari, Apameh, McCleary, Kaci, Moriarty, Gerald, Nichols, Kendall, Ghannam, Malik, Brown, Kevin, Berry, Brent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404554/
https://www.ncbi.nlm.nih.gov/pubmed/36008800
http://dx.doi.org/10.1186/s12883-022-02849-1
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author Puram, Vikram V.
Ghazaleh, Dana
Salari, Apameh
McCleary, Kaci
Moriarty, Gerald
Nichols, Kendall
Ghannam, Malik
Brown, Kevin
Berry, Brent
author_facet Puram, Vikram V.
Ghazaleh, Dana
Salari, Apameh
McCleary, Kaci
Moriarty, Gerald
Nichols, Kendall
Ghannam, Malik
Brown, Kevin
Berry, Brent
author_sort Puram, Vikram V.
collection PubMed
description BACKGROUND: Posterior Reversible Encephalopathy Syndrome (PRES) is a neurotoxic state characterized by seizures, headache, vision change, paresis, and altered mental status. PRES has an important place in medicine due to the wide variety of causative diseases, infections, and medications that precipitate its mysterious onset. Although exposure to medications, particularly immunosuppressants, cancer chemotherapy, and biologic drugs, is a common occurrence in patients who develop PRES, Mepolizumab has never before been associated. CASE PRESENTATION: This report of a 67-year-old male patient outlines the first reported case of Mepolizumab-induced PRES in the literature. CONCLUSIONS: Treatment of severe asthma, asthma-exacerbations, and diseases such as eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss) with Mepolizumab is rapidly gaining popularity ever since the drug’s recent FDA-approval. This report aims to raise awareness of this potentially life-threatening and previously unreported side effect of Mepolizumab since early identification of the causative agent is the key to preventing the severe neurologic disability and possible death that may occur from the delayed treatment of PRES.
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spelling pubmed-94045542022-08-26 Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report Puram, Vikram V. Ghazaleh, Dana Salari, Apameh McCleary, Kaci Moriarty, Gerald Nichols, Kendall Ghannam, Malik Brown, Kevin Berry, Brent BMC Neurol Case Report BACKGROUND: Posterior Reversible Encephalopathy Syndrome (PRES) is a neurotoxic state characterized by seizures, headache, vision change, paresis, and altered mental status. PRES has an important place in medicine due to the wide variety of causative diseases, infections, and medications that precipitate its mysterious onset. Although exposure to medications, particularly immunosuppressants, cancer chemotherapy, and biologic drugs, is a common occurrence in patients who develop PRES, Mepolizumab has never before been associated. CASE PRESENTATION: This report of a 67-year-old male patient outlines the first reported case of Mepolizumab-induced PRES in the literature. CONCLUSIONS: Treatment of severe asthma, asthma-exacerbations, and diseases such as eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss) with Mepolizumab is rapidly gaining popularity ever since the drug’s recent FDA-approval. This report aims to raise awareness of this potentially life-threatening and previously unreported side effect of Mepolizumab since early identification of the causative agent is the key to preventing the severe neurologic disability and possible death that may occur from the delayed treatment of PRES. BioMed Central 2022-08-25 /pmc/articles/PMC9404554/ /pubmed/36008800 http://dx.doi.org/10.1186/s12883-022-02849-1 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
Puram, Vikram V.
Ghazaleh, Dana
Salari, Apameh
McCleary, Kaci
Moriarty, Gerald
Nichols, Kendall
Ghannam, Malik
Brown, Kevin
Berry, Brent
Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title_full Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title_fullStr Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title_full_unstemmed Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title_short Mepolizumab-Induced Posterior Reversible Encephalopathy Syndrome (PRES), a new patient report
title_sort mepolizumab-induced posterior reversible encephalopathy syndrome (pres), a new patient report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404554/
https://www.ncbi.nlm.nih.gov/pubmed/36008800
http://dx.doi.org/10.1186/s12883-022-02849-1
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