Abstract

Posterior reversible encephalopathy syndrome (PRES) is a rare complication of a sudden rise in blood pressure. It is seen in hypertensive patients. It is a clinical–radiological entity characterized by the association of neurological clinical signs and bilateral posterior cerebral edema usually reversible in neuroimaging. According to the literature, it is quite common in adults than in children. The most common causes are hypertensive encephalopathy, renal failure, central nervous system vasculitis, electrolyte disturbances, or when using cytotoxic or immunosuppressive therapies. It is clinically manifested as headache, seizures, coma, or visual disturbances. Imaging plays an undeniable role in the diagnosis and surveillance and cerebral magnetic resonance imaging (MRI) reveals bilateral and asymmetrical lesions affecting the basal ganglia, the left frontal lobe and the parietal lobes, in the form of hyperintensities in sequences. T2 and fluid-attenuated inversion recovery (FLAIR) imaging lead to vasogenic edema. The treatment of the basic pathology is the key to the reversibility of this syndrome. We report this article with the aim of retrieving and demonstrating the interest of imaging as part of a diagnostic approach and monitoring of PRES in a 54-year-old subject followed for schizophrenia and arterial hypertension under neuroleptic treatment having presented seizures with high blood pressure after 10 days of this neuroleptic treatment. The clinical course is favorable without recurrence of crisis with disappearance of the lesions on the imaging of the control after the interruption of the neuroleptics and the normalization of the arterial tension, living and asymptomatic patient on a retreat of one year.

Highlights

  • Posterior reversible encephalopathy syndrome (PRES) is an entity described for about 20 years

  • Posterior reversible encephalopathy (RPE) is a clinicoradiological entity associating a reversible damage of the central nervous system with a typical encephalic imaging [magnetic resonance imaging (MRI) or computed tomography (CT)]

  • Several etiologies may be at the origin of this syndrome, they are dominated by hypertensive encephalopathy [7], pre-eclampsia, eclampsia [2], immunosuppressive therapies, and renal disorders [2]

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Summary

INTRODUCTION

Posterior reversible encephalopathy syndrome (PRES) is an entity described for about 20 years. This clinical and neuroradiological condition was first reported by Hinchey in 1996 [1]. Even if endothelial function plays a major role, with loss of cerebrovascular autoregulation and rupture of the blood–brain barrier (BBB) leading to cerebral edema This diagnosis is mainly evoked in patients with neurological symptoms, in the context of renal failure, International Journal of Case Reports and Images, Vol 11, 2020. Cerebral MRI demonstrated T1 hypointensity and proton density hyperintensity in T2 and FLAIR in the subcortical white matter was reflected in bilateral and symmetrical hypersignals of interest to the left frontal lobe and posterior parietal lobes and basal ganglia, which led to vasogenic edema (Figure 1). Autoimmune encephalitis and metabolic encephalopathies, such as deranged serum glucose, sodium (including central pontine myelinolysis), uremia, or drug toxicity (e.g., cyclosporine) can have similar

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