4.5 Article

Susceptibility-weighted imaging reveals cerebral microvascular injury in severe COVID-19

期刊

出版社

ELSEVIER
DOI: 10.1016/j.jns.2021.117308

关键词

COVID-19; MRI; Susceptibility-weighted imaging; Coma

资金

  1. James S. McDonnell Foundation COVID-19 Recovery of Consciousness Consortium
  2. NIH National Institute of Neurological Disorders and Stroke [R21NS109627, R21AG067562, RF1NS115268]
  3. NIH Director's Office [DP2HD101400]
  4. NIH National Institute of Mental Health [K23MH115812]
  5. Tiny Blue Dot Foundation
  6. Harvard University Eleanor and Miles Shore Fellowship Program
  7. NIH National Institutes of Allergy and Infectious Diseases [2U19AI110818]

向作者/读者索取更多资源

In patients with severe COVID-19, microvascular brain lesions, characterized by punctate SWI lesions, are commonly found in the subcortical and deep white matter. These lesions are associated with widespread microvascular injury, indicating a risk for hemorrhagic and ischemic lesions in the brain.
We evaluated the incidence, distribution, and histopathologic correlates of microvascular brain lesions in patients with severe COVID-19. Sixteen consecutive patients admitted to the intensive care unit with severe COVID19 undergoing brain MRI for evaluation of coma or neurologic deficits were retrospectively identified. Eleven patients had punctate susceptibility-weighted imaging (SWI) lesions in the subcortical and deep white matter, eight patients had >10 SWI lesions, and four patients had lesions involving the corpus callosum. The distribution of SWI lesions was similar to that seen in patients with hypoxic respiratory failure, sepsis, and disseminated intravascular coagulation. Brain autopsy in one patient revealed that SWI lesions corresponded to widespread microvascular injury, characterized by perivascular and parenchymal petechial hemorrhages and microscopic ischemic lesions. Collectively, these radiologic and histopathologic findings add to growing evidence that patients with severe COVID-19 are at risk for multifocal microvascular hemorrhagic and ischemic lesions in the subcortical and deep white matter.

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