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Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature

BACKGROUND: Treatment options for chronic osmotic demyelination syndrome are limited to case reports and only a very few show complete recovery. We report a case of complete recovery of chronic osmotic demyelination syndrome with plasmapheresis. CASE PRESENTATION: A 43-year-old Sri Lankan man presen...

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Autores principales: Wijayabandara, Maheshi, Appuhamy, Shenal, Weerathunga, Praveen, Chang, Thashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798224/
https://www.ncbi.nlm.nih.gov/pubmed/33430956
http://dx.doi.org/10.1186/s13256-020-02573-9
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author Wijayabandara, Maheshi
Appuhamy, Shenal
Weerathunga, Praveen
Chang, Thashi
author_facet Wijayabandara, Maheshi
Appuhamy, Shenal
Weerathunga, Praveen
Chang, Thashi
author_sort Wijayabandara, Maheshi
collection PubMed
description BACKGROUND: Treatment options for chronic osmotic demyelination syndrome are limited to case reports and only a very few show complete recovery. We report a case of complete recovery of chronic osmotic demyelination syndrome with plasmapheresis. CASE PRESENTATION: A 43-year-old Sri Lankan man presented with fever, repeated vomiting, unsteady gait, increased tonicity of his right upper limb and paucity of speech for three days. He was treated in the local hospital with antibiotics and antivirals as per central nervous system infection. He had hyponatraemia, which was rapidly corrected with hypertonic saline from 97 to 119 mmol/L. He was transferred to our hospital because of progressive reduction of consciousness, rapidly worsening rigidity and bradykinesia of all four limbs and worsening dysarthria and bradyphrenia. Magnetic resonance imaging of the brain was compatible with osmotic demyelination syndrome. He was commenced on plasmapheresis twenty-two days after rapid correction of sodium. He regained independent mobility with complete resolution of rigidity, bradykinesia and speech dysfunction after five cycles of alternate day plasmapheresis. CONCLUSION: Plasmapheresis can be considered as an effective treatment modality in chronic osmotic demyelination syndrome.
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spelling pubmed-77982242021-01-11 Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature Wijayabandara, Maheshi Appuhamy, Shenal Weerathunga, Praveen Chang, Thashi J Med Case Rep Case Report BACKGROUND: Treatment options for chronic osmotic demyelination syndrome are limited to case reports and only a very few show complete recovery. We report a case of complete recovery of chronic osmotic demyelination syndrome with plasmapheresis. CASE PRESENTATION: A 43-year-old Sri Lankan man presented with fever, repeated vomiting, unsteady gait, increased tonicity of his right upper limb and paucity of speech for three days. He was treated in the local hospital with antibiotics and antivirals as per central nervous system infection. He had hyponatraemia, which was rapidly corrected with hypertonic saline from 97 to 119 mmol/L. He was transferred to our hospital because of progressive reduction of consciousness, rapidly worsening rigidity and bradykinesia of all four limbs and worsening dysarthria and bradyphrenia. Magnetic resonance imaging of the brain was compatible with osmotic demyelination syndrome. He was commenced on plasmapheresis twenty-two days after rapid correction of sodium. He regained independent mobility with complete resolution of rigidity, bradykinesia and speech dysfunction after five cycles of alternate day plasmapheresis. CONCLUSION: Plasmapheresis can be considered as an effective treatment modality in chronic osmotic demyelination syndrome. BioMed Central 2021-01-11 /pmc/articles/PMC7798224/ /pubmed/33430956 http://dx.doi.org/10.1186/s13256-020-02573-9 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Wijayabandara, Maheshi
Appuhamy, Shenal
Weerathunga, Praveen
Chang, Thashi
Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title_full Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title_fullStr Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title_full_unstemmed Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title_short Effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
title_sort effective treatment of osmotic demyelination syndrome with plasmapheresis: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798224/
https://www.ncbi.nlm.nih.gov/pubmed/33430956
http://dx.doi.org/10.1186/s13256-020-02573-9
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