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A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination

Central pontine myelinolysis (CPM) is a neurological demyelinating disease of the pons. Although usually associated with rapid correction of hyponatremia, CPM may occur despite normonatremia, is often associated with chronic alcoholism and may be asymptomatic. Histological confirmation of asymptomat...

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Autores principales: Haynes, Harry R., Gallagher, Patrick J., Cordaro, Andrea, Likeman, Marcus, Love, Seth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830465/
https://www.ncbi.nlm.nih.gov/pubmed/29177819
http://dx.doi.org/10.1007/s12024-017-9933-y
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author Haynes, Harry R.
Gallagher, Patrick J.
Cordaro, Andrea
Likeman, Marcus
Love, Seth
author_facet Haynes, Harry R.
Gallagher, Patrick J.
Cordaro, Andrea
Likeman, Marcus
Love, Seth
author_sort Haynes, Harry R.
collection PubMed
description Central pontine myelinolysis (CPM) is a neurological demyelinating disease of the pons. Although usually associated with rapid correction of hyponatremia, CPM may occur despite normonatremia, is often associated with chronic alcoholism and may be asymptomatic. Histological confirmation of asymptomatic CPM is rare. We describe an unusual post-mortem case of extensive but asymptomatic CPM in a chronic alcoholic patient with normonatremia. The affected part of the pons contained thinly myelinated axons with appearances supporting remyelination. We suggest that remyelination may account for the subclinical nature of this patient's CPM.
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spelling pubmed-58304652018-03-05 A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination Haynes, Harry R. Gallagher, Patrick J. Cordaro, Andrea Likeman, Marcus Love, Seth Forensic Sci Med Pathol Case Report Central pontine myelinolysis (CPM) is a neurological demyelinating disease of the pons. Although usually associated with rapid correction of hyponatremia, CPM may occur despite normonatremia, is often associated with chronic alcoholism and may be asymptomatic. Histological confirmation of asymptomatic CPM is rare. We describe an unusual post-mortem case of extensive but asymptomatic CPM in a chronic alcoholic patient with normonatremia. The affected part of the pons contained thinly myelinated axons with appearances supporting remyelination. We suggest that remyelination may account for the subclinical nature of this patient's CPM. Springer US 2017-11-25 2018 /pmc/articles/PMC5830465/ /pubmed/29177819 http://dx.doi.org/10.1007/s12024-017-9933-y Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Haynes, Harry R.
Gallagher, Patrick J.
Cordaro, Andrea
Likeman, Marcus
Love, Seth
A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title_full A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title_fullStr A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title_full_unstemmed A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title_short A case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
title_sort case of chronic asymptomatic central pontine myelinolysis with histological evidence of remyelination
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830465/
https://www.ncbi.nlm.nih.gov/pubmed/29177819
http://dx.doi.org/10.1007/s12024-017-9933-y
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