Revision 50 for 'Posterior reversible encephalopathy syndrome'

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Posterior reversible encephalopathy syndrome

Posterior reversible encephalopathy syndrome (PRES), also known as hypertensive encephalopathy, is a neurotoxic state that occurs secondary to the inability of posterior circulation to auto-regulate in response to acute changes in blood pressure. Hyperperfusion with resultant disruption of the blood brain barrier results in vasogenic oedema, but no infarction, most commonly in the parieto-occipital regions.

It should not be confused with chronic hypertensive encephalopathy, also know as hypertensive microangiopathy, which results in microhemorrhages in the basal ganglia, pons and cerebellum.


The syndrome can be precipitated by various clinical settings. The mechanism is not well understood but is thought to be related to altered integrity of the blood brain barrier.

There are two main theories:

  1. High blood pressure leads to loss of self-regulation, hyper-perfusion with endothelial damage and vasogenic edema.
  2. Endothelial dysfunction leads to vasoconstriction and hypo-perfusion resulting in cerebral ischemia and subsequent vasogenic edema.

Hypertension is not present or not reach the upper limits to self-regulation ( 150-160 mmHg ) in 25% of patients.


Radiographic features

Most commonly there is vasogenic oedema within the occipital and parietal regions (~95% of cases), perhaps relating to the posterior cerebral artery supply. The oedema is usually symmetrical. Despite being termed posterior, PRES can be found in a non posterior distribution, mainly in watershed areas, including within the frontal, inferior temporal, cerebellar and brainstem regions 2. Both cortical and subcortical locations are affected.

There are three main imaging patterns:

  1. holohemispheric at watershed zones
  2. superior frontal sulcus
  3. parieto-occipital dominance

Parenchymal infarctions and hemorrhage are associated with PRES in respectively 10-25% and 15% of cases.


Affected regions are hypoattenuating.

  • T1: hypo intense in affected region(s)
  • C+ (Gd): patchy variable enhancement
  • T2:  hyperintense in affected region(s)
  • DWI: usually normal
  • ADC: signal increased in affected regions due to increased diffusion
  • GRE: may show hypointense signal in cases of haemorrhage

Differential diagnosis

General imaging differential considerations include:

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