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Opioid-Induced Leukoencephalopathies: A Report of Two Cases
Acute toxic leukoencephalopathy (ATL) and delayed post-hypoxic leukoencephalopathy (DPHL) are two possible adverse entities related to opioid intoxication (OI), each having a distinct clinical course. While ATL shows a monophasic course with gradual neurological deterioration, DPHL has a distinct bi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832237/ https://www.ncbi.nlm.nih.gov/pubmed/35221972 http://dx.doi.org/10.1159/000521410 |
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author | Knudsen, Gustav Højrup Kermanian, Nata Kock-Jensen, Carsten Hanshelge Antulov, Ronald |
author_facet | Knudsen, Gustav Højrup Kermanian, Nata Kock-Jensen, Carsten Hanshelge Antulov, Ronald |
author_sort | Knudsen, Gustav Højrup |
collection | PubMed |
description | Acute toxic leukoencephalopathy (ATL) and delayed post-hypoxic leukoencephalopathy (DPHL) are two possible adverse entities related to opioid intoxication (OI), each having a distinct clinical course. While ATL shows a monophasic course with gradual neurological deterioration, DPHL has a distinct biphasic course. We report a case of ATL along with a case of DPHL happening in young male patients with OI, including their clinical courses as well as imaging characteristics with comparable time intervals. Initially, both leukoencephalopathies typically show magnetic resonance imaging findings with confluent and symmetric white matter (WM) abnormalities in the periventricular regions on T2 and fluid-attenuated inversion recovery images along with restricted diffusion on diffusion-weighted imaging. The DPHL patient however also presented with WM cystic substance loss in the deterioration phase, several weeks after hospital admission, which was previously described in a case of DPHL. Interestingly, similar WM changes have recently been observed in virus-associated necrotizing disseminated acute leukoencephalopathy in patients with coronavirus disease 2019 which may suggest a common pathophysiological mechanism. Knowing the distinct imaging features of ATL and DPHL along with their typical clinical courses can provide a faster and more reliable differentiation between these two entities. |
format | Online Article Text |
id | pubmed-8832237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-88322372022-02-25 Opioid-Induced Leukoencephalopathies: A Report of Two Cases Knudsen, Gustav Højrup Kermanian, Nata Kock-Jensen, Carsten Hanshelge Antulov, Ronald Case Rep Neurol Single Case − General Neurology Acute toxic leukoencephalopathy (ATL) and delayed post-hypoxic leukoencephalopathy (DPHL) are two possible adverse entities related to opioid intoxication (OI), each having a distinct clinical course. While ATL shows a monophasic course with gradual neurological deterioration, DPHL has a distinct biphasic course. We report a case of ATL along with a case of DPHL happening in young male patients with OI, including their clinical courses as well as imaging characteristics with comparable time intervals. Initially, both leukoencephalopathies typically show magnetic resonance imaging findings with confluent and symmetric white matter (WM) abnormalities in the periventricular regions on T2 and fluid-attenuated inversion recovery images along with restricted diffusion on diffusion-weighted imaging. The DPHL patient however also presented with WM cystic substance loss in the deterioration phase, several weeks after hospital admission, which was previously described in a case of DPHL. Interestingly, similar WM changes have recently been observed in virus-associated necrotizing disseminated acute leukoencephalopathy in patients with coronavirus disease 2019 which may suggest a common pathophysiological mechanism. Knowing the distinct imaging features of ATL and DPHL along with their typical clinical courses can provide a faster and more reliable differentiation between these two entities. S. Karger AG 2022-02-01 /pmc/articles/PMC8832237/ /pubmed/35221972 http://dx.doi.org/10.1159/000521410 Text en Copyright © 2022 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case − General Neurology Knudsen, Gustav Højrup Kermanian, Nata Kock-Jensen, Carsten Hanshelge Antulov, Ronald Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title | Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title_full | Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title_fullStr | Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title_full_unstemmed | Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title_short | Opioid-Induced Leukoencephalopathies: A Report of Two Cases |
title_sort | opioid-induced leukoencephalopathies: a report of two cases |
topic | Single Case − General Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832237/ https://www.ncbi.nlm.nih.gov/pubmed/35221972 http://dx.doi.org/10.1159/000521410 |
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