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Leukoaraiosis

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Encyclopedia of Clinical Neuropsychology
  • 31 Accesses

Synonyms

Periventricular leukoencephalopathy (PVL); Small vessel disease; White matter disease; White matter hyperintensity (WMH)

Definition

Leukoaraiosis is a radiological diagnosis referring to rarefaction of white matter and describes brain pathology characterized by diffuse, confluent white matter abnormalities, typically in the periventricular regions of the brain. Most associated with disease of the small vessels, leukoaraiosis is thought to reflect chronic low-level ischemia in combination with blood-brain barrier dysfunction. Additionally, it may be associated with blood vessel abnormalities, other ischemic events, edema, and cerebral amyloid angiopathy. The underlying pathology includes myelin pallor, enlargement of perivascular spaces, gliosis, axonal loss, and ischemic demyelination. Vascular risk factors, such as hypertension, heart disease, or diabetes, and increasing age are risk factors for developing leukoaraiosis. Leukoaraiosis is detectable by high-frequency CT and...

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References and Readings

  • Grueter, B. E., & Schulz, U. G. (2012). Age-related cerebral white matter disease (leukoaraiosis): A review. Postgraduate Medical Journal, 88, 79–87.

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  • Miki, Y., & Sakamoto, S. (2013). Age-related white matter lesions (Leukoaraiosis): An update. Brain and Nerve, 65(7), 789–799.

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  • O’Sullivan, M. (2008). Leukoaraiosis. Practical Neurology, 8, 26–38.

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  • Pantoni, L., & Garcia, J. H. (1995). The signficance of cerebral white matter abnormalities 100 years after Binswanger’s report: A review. Stroke, 26, 1293–1301.

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  • Pantoni, L., & Garcia, J. H. (1997). Pathogenesis of leukoaraiosis: A review. Stroke, 28, 652–659.

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  • Pantoni, L., & Inzitari, D. (1998). New clinical relevance of leukoaraiosis. Stroke, 29(2), 543.

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Correspondence to Yana Suchy .

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Suchy, Y., Eastvold, A. (2017). Leukoaraiosis. In: Kreutzer, J., DeLuca, J., Caplan, B. (eds) Encyclopedia of Clinical Neuropsychology. Springer, Cham. https://doi.org/10.1007/978-3-319-56782-2_499-2

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  • DOI: https://doi.org/10.1007/978-3-319-56782-2_499-2

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