Abstract
Posterior reversible encephalopathy syndrome was described in 1996 as a clinical-neuroimaging entity characterized by parietooccipital watershed-region edema without overt infarction. It has been linked to hypertension, eclampsia, immunosuppressive therapies, infections, and autoimmune disorders. The condition usually has an acute onset, presents with seizures, and ameliorates within days. There have been few neuropathological studies, but in some cases, tissue damage may be more permanent.
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Willard, N., Honce, J. M., & Kleinschmidt-DeMasters, B. K. (2018, February 1). PRES: Review of histological features. Journal of Neuropathology and Experimental Neurology. Oxford University Press. https://doi.org/10.1093/jnen/nlx112
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