Osmotic demyelination syndrome, a case report.

Authors

  • Javier Rodríguez Jiménez Hospital Clínico Universitario de Valladolid

DOI:

https://doi.org/10.53903/01212095.151

Keywords:

Myelinolysis, central pontine, Neuroimaging, Magnetic resonance imaging

Abstract

Osmotic demyelination syndrome, previously known as central pontine myelinolysis, is a known disorder in patients with severe hyponatremia in whom rapid sodium correction is performed. It is clinically described as a pseudobulbar palsy, comprised of tetraparesis, encephalopathy, rigidity,
ataxia and abnormal movements. It consists of a non-inflammatory demyelination secondary to severe neuronal edema at the pons and other extrapontine locations. It is a very rare pathology, with a poor prognosis and whose only treatment is rehabilitation. A case of a 51-year-old man with fast progressive neurological deficit following rapid correction of severe hyponatremia is presented. The patient required orotracheal intubation due to clinical deteroriation and was diagnosed by computed tomography (CT) and  confirmed by magnetic resonance imaging (MRI).

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References

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DeWitt LD, Buonanno FS, Kistler JP, et al. Central pon-tine myelinolysis: demonstration by nuclear magnetic resonance. Neurology. 1984;34(5):570-6.

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Published

2022-03-30

How to Cite

(1)
Rodríguez Jiménez, J. Osmotic Demyelination Syndrome, a Case Report. Rev. colomb. radiol. 2022, 33, 5714-5716.

Issue

Section

Case reports
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