AI Article Synopsis

  • Neurologic symptoms are frequently observed in COVID-19, with demyelination identified as a significant neuropathological change, but its exact causes are still unclear.
  • A case study revealed extensive demyelination in the medulla oblongata, spinal canal, and cerebrum of a COVID-19 patient who died from sepsis, with unique patterns of demyelination suggesting distinct pathways of viral spread.
  • The demyelination patterns observed in the patient may have been influenced by pre-existing conditions such as diabetes, hypertension, and spinal canal stenosis.

Article Abstract

Neurologic symptoms are common in COVID-19, and a variety of neuropathological changes have been reported. One of the important neuropathological findings is demyelination. However, the underlying pathogenesis of demyelination remained poorly understood. We witnessed a case of COVID-19 with distinct types of demyelination in the cerebrum, medulla oblongata, and spinal canal, who died of sepsis. The postmortem examination showed the solitary massive demyelination in the medulla oblongata. The massive lesion was filled with components of perineuronal nets. In the spinal canal, confluent demyelination in bilateral lateral and dorsal funiculi was detected over the entire length from C1 to S5, which was maximum at the level of cervical spinal canal stenosis. Demyelination in the cerebrum was mainly perivenular, and augmented in the area of lacunar infarcts and dilated perivascular spaces. Considering the distribution patterns of the following three types of demyelination, the traces of viral spreading could be highlighted. Discontinuous perivenous demyelination in the cerebrum showed the result of hematogenous spreading. Longitudinal confluent demyelination of the spinal cord should be the picturesque of the trace of axonal spreading. The distribution of demyelination was possibly modified by the underlying diseases, diabetes mellitus, hypertension, and spinal canal stenosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10805624PMC
http://dx.doi.org/10.7759/cureus.51049DOI Listing

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