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Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report

Acute necrotizing encephalopathy (ANE) is a rare but distinctive type of influenza-associated encephalopathy characterized by symmetric multiple lesions with an invariable thalamic involvement. Although the exact pathogenesis of ANE remains unclear, the most prevalent hypothesis is the “cytokine sto...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Radiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432353/
https://www.ncbi.nlm.nih.gov/pubmed/36238398
http://dx.doi.org/10.3348/jksr.2020.0173
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description Acute necrotizing encephalopathy (ANE) is a rare but distinctive type of influenza-associated encephalopathy characterized by symmetric multiple lesions with an invariable thalamic involvement. Although the exact pathogenesis of ANE remains unclear, the most prevalent hypothesis is the “cytokine storm,” which results in blood-brain-barrier breakdown. We present the case of a 10-year-old boy with fulminant ANE confirmed with serial MRI studies, including diffusion-weighted imaging and susceptibility-weighted imaging. A comparison of these serial images demonstrated detailed and longitudinal changes in MRI findings during the clinical course corresponding to pathophysiological changes. Our case clarifies the pathogenesis of ANE brain lesions using serial imaging studies and suggests that early immunomodulatory therapy reduces brain damage.
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spelling pubmed-94323532022-10-12 Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report Taehan Yongsang Uihakhoe Chi Neuroradiology & Neurointervention Acute necrotizing encephalopathy (ANE) is a rare but distinctive type of influenza-associated encephalopathy characterized by symmetric multiple lesions with an invariable thalamic involvement. Although the exact pathogenesis of ANE remains unclear, the most prevalent hypothesis is the “cytokine storm,” which results in blood-brain-barrier breakdown. We present the case of a 10-year-old boy with fulminant ANE confirmed with serial MRI studies, including diffusion-weighted imaging and susceptibility-weighted imaging. A comparison of these serial images demonstrated detailed and longitudinal changes in MRI findings during the clinical course corresponding to pathophysiological changes. Our case clarifies the pathogenesis of ANE brain lesions using serial imaging studies and suggests that early immunomodulatory therapy reduces brain damage. The Korean Society of Radiology 2021-09 2021-07-14 /pmc/articles/PMC9432353/ /pubmed/36238398 http://dx.doi.org/10.3348/jksr.2020.0173 Text en Copyrights © 2021 The Korean Society of Radiology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroradiology & Neurointervention
Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title_full Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title_fullStr Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title_full_unstemmed Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title_short Fulminant Course of Acute Necrotizing Encephalopathy Followed by Serial MRI: A Case Report
title_sort fulminant course of acute necrotizing encephalopathy followed by serial mri: a case report
topic Neuroradiology & Neurointervention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432353/
https://www.ncbi.nlm.nih.gov/pubmed/36238398
http://dx.doi.org/10.3348/jksr.2020.0173
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