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Posterior reversible encephalopathy syndrome (PRES): diagnosis and management
James D Triplett1, Mansur Amirovich Kutlubaev2, Allan G Kermode3,4
1Neurology, Concord Hospital, Concord, New South Wales, Australia James.triplett@health.nsw.gov.au.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) may present with diverse clinical symptoms including visual disturbance, headache, seizures and impaired consciousness. MRI shows oedema, usually involving the posterior subcortical regions. Triggering factors include hypertension, pre-eclampsia/eclampsia, renal failure, cytotoxic agents and autoimmune conditions. The mechanism underlying PRES is not certain, but endothelial dysfunction is implicated. Treatment is supportive and involves correcting the underlying cause and managing associated complications, such as seizures. Although most patients recover, PRES is not always reversible and may be associated with considerable morbidity and even mortality.
Insights
Posterior reversible encephalopathy syndrome (PRES) presents with varied symptoms like seizures and vision loss, often linked to high blood pressure. While typically reversible, PRES can lead to serious complications.
Area of Science:
- Neurology
- Radiology
- Internal Medicine
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition with diverse clinical presentations.
- It is characterized by brain edema, predominantly in posterior subcortical areas, visible on MRI.
- PRES is associated with various conditions including hypertension, pre-eclampsia, renal failure, and autoimmune disorders.
Purpose of the Study:
- To summarize the clinical presentation, radiological findings, triggering factors, and outcomes of Posterior Reversible Encephalopathy Syndrome (PRES).
- To highlight the implicated mechanisms and current treatment strategies for PRES.
Main Methods:
- Review of clinical symptoms such as visual disturbance, headache, seizures, and impaired consciousness.
- Magnetic Resonance Imaging (MRI) findings focusing on characteristic edema patterns.
- Analysis of common triggering factors and implicated pathophysiological mechanisms, particularly endothelial dysfunction.
Main Results:
- PRES manifests with a range of neurological deficits and characteristic posterior brain edema on MRI.
- Identified triggers include hypertension, pre-eclampsia/eclampsia, renal failure, cytotoxic agents, and autoimmune diseases.
- Endothelial dysfunction is a key implicated mechanism, though not fully understood.
Conclusions:
- PRES is a syndrome with varied clinical and radiological features, often triggered by specific medical conditions.
- While supportive treatment and management of underlying causes can lead to recovery, PRES carries risks of significant morbidity and mortality.
- Further research into the precise mechanisms may improve diagnostic and therapeutic approaches for PRES.
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