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December 08, 2015; 85 (23) Editorial

Small DWI lesions after intracerebral hemorrhage

Are perivascular spaces the missing link?

Christopher D. Anderson, Andreas Charidimou
First published November 6, 2015, DOI: https://doi.org/10.1212/WNL.0000000000002181
Christopher D. Anderson
From the Center for Human Genetic Research (C.D.A.), The J. Philip Kistler Stroke Research Center (C.D.A.), and Hemorrhagic Stroke Research Program (A.C.), Massachusetts General Hospital, Boston; and University College London Institute of Neurology and The National Hospital for Neurology and Neurosurgery (A.C.), London, UK.
MD, MMSc
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Andreas Charidimou
From the Center for Human Genetic Research (C.D.A.), The J. Philip Kistler Stroke Research Center (C.D.A.), and Hemorrhagic Stroke Research Program (A.C.), Massachusetts General Hospital, Boston; and University College London Institute of Neurology and The National Hospital for Neurology and Neurosurgery (A.C.), London, UK.
MD, PhD
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Citation
Small DWI lesions after intracerebral hemorrhage
Are perivascular spaces the missing link?
Christopher D. Anderson, Andreas Charidimou
Neurology Dec 2015, 85 (23) 2004-2005; DOI: 10.1212/WNL.0000000000002181

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The MRI era has provided vascular neurologists with a number of novel imaging markers that associate with clinical outcomes in stroke and cerebrovascular disease. Examples include periventricular white mater hyperintensities, lobar and deep cerebral microbleeds, cortical superficial siderosis, and cerebral microinfarcts.1,2 Recently, MRI-visible perivascular spaces (or Virchow-Robin spaces) have been associated with both deep and lobar intracerebral hemorrhage (ICH),3 and have therefore garnered increasing attention. Although classically thought of as extensions of the subarachnoid space coursing with penetrating cerebral vessels, evolving data suggest that Virchow-Robin spaces may actually be interstitial fluid-filled cavities and not contiguous with the subarachnoid space.4 While it is not yet clear whether all MRI-visible perivascular spaces carry the same risk implications across patient populations, their frequent coexistence on MRI and spatial association with incident ICH raise the hypothesis that they represent another imaging marker of cerebral small vessel disease and may therefore provide clues regarding the initiation and progression of related clinical and imaging phenotypes.

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  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the editorial.

  • See page 2045

  • © 2015 American Academy of Neurology
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