Osmotic demyelination syndrome despite appropriate gradual correction of moderate hyponatraemia.

ALCOHOL-RELATED PROBLEMS BEHCET-S SYNDROME BLOOD-BRAIN BARRIER LIVER DISEASE

Journal

Practical neurology
ISSN: 1474-7766
Titre abrégé: Pract Neurol
Pays: England
ID NLM: 101130961

Informations de publication

Date de publication:
16 May 2022
Historique:
accepted: 26 04 2022
entrez: 16 5 2022
pubmed: 17 5 2022
medline: 17 5 2022
Statut: aheadofprint

Résumé

Osmotic demyelination syndrome characteristically follows rapid correction of hyponatraemia. We present a young woman with a subacute progressive brainstem syndrome and diffuse pontine signal abnormality on MR imaging, diagnosed as osmotic demyelination syndrome. The case posed a diagnostic challenge due to comorbid Behçet's disease and the absence of significant fluctuation in her serum sodium concentration. Osmotic demyelination syndrome is not limited to patients with rapidly corrected hyponatraemia, especially when there are other risk factors. These factors, all present in this patient, include hypokalaemia, hypophosphataemia, malnutrition, harmful alcohol use and liver dysfunction.

Identifiants

pubmed: 35577547
pii: practneurol-2022-003369
doi: 10.1136/practneurol-2022-003369
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Patrick Thomas Murphy (PT)

Department of Neurology, Imperial College Healthcare NHS Trust, London, UK patrick.murphy9@nhs.net.

Stephen Auger (S)

Department of Neurology, Imperial College Healthcare NHS Trust, London, UK.

Ashwini Nandoskar (A)

Department of Neurology, Imperial College Healthcare NHS Trust, London, UK.

Classifications MeSH