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Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults

Delayed post-hypoxic leukoencephalopathy (DPHL) is an uncommon, potentially under-recognized, cause of hypoxia induced white matter injury. It characteristically follows a biphasic course: After an initial phase of altered neurologic status a recovery occurs which is then followed by a recurring pha...

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Autores principales: Beeskow, Anne B., Oberstadt, Moritz, Saur, Dorothee, Hoffmann, Karl-Titus, Lobsien, Donald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119709/
https://www.ncbi.nlm.nih.gov/pubmed/30210433
http://dx.doi.org/10.3389/fneur.2018.00708
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author Beeskow, Anne B.
Oberstadt, Moritz
Saur, Dorothee
Hoffmann, Karl-Titus
Lobsien, Donald
author_facet Beeskow, Anne B.
Oberstadt, Moritz
Saur, Dorothee
Hoffmann, Karl-Titus
Lobsien, Donald
author_sort Beeskow, Anne B.
collection PubMed
description Delayed post-hypoxic leukoencephalopathy (DPHL) is an uncommon, potentially under-recognized, cause of hypoxia induced white matter injury. It characteristically follows a biphasic course: After an initial phase of altered neurologic status a recovery occurs which is then followed by a recurring phase of neurologic deterioration, typically 2–4 weeks after the initial event. At this time white matter changes can be identified on MRI, which are the hallmark of DPHL. The characteristics and the typical MR-imaging signs of DPHL are discussed in this case report.
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spelling pubmed-61197092018-09-12 Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults Beeskow, Anne B. Oberstadt, Moritz Saur, Dorothee Hoffmann, Karl-Titus Lobsien, Donald Front Neurol Neurology Delayed post-hypoxic leukoencephalopathy (DPHL) is an uncommon, potentially under-recognized, cause of hypoxia induced white matter injury. It characteristically follows a biphasic course: After an initial phase of altered neurologic status a recovery occurs which is then followed by a recurring phase of neurologic deterioration, typically 2–4 weeks after the initial event. At this time white matter changes can be identified on MRI, which are the hallmark of DPHL. The characteristics and the typical MR-imaging signs of DPHL are discussed in this case report. Frontiers Media S.A. 2018-08-27 /pmc/articles/PMC6119709/ /pubmed/30210433 http://dx.doi.org/10.3389/fneur.2018.00708 Text en Copyright © 2018 Beeskow, Oberstadt, Saur, Hoffmann and Lobsien. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Beeskow, Anne B.
Oberstadt, Moritz
Saur, Dorothee
Hoffmann, Karl-Titus
Lobsien, Donald
Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title_full Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title_fullStr Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title_full_unstemmed Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title_short Delayed Post-hypoxic Leukoencephalopathy (DPHL)—An Uncommon Variant of Hypoxic Brain Damage in Adults
title_sort delayed post-hypoxic leukoencephalopathy (dphl)—an uncommon variant of hypoxic brain damage in adults
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119709/
https://www.ncbi.nlm.nih.gov/pubmed/30210433
http://dx.doi.org/10.3389/fneur.2018.00708
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