Posterior reversible encephalopathy syndrome (PRES)

Case contributed by Yari Anahi Ramos
Diagnosis almost certain

Presentation

Acute post-infectious glomerulonephritis secondary to streptococcal pharyngotonsillitis, where he reported blood pressure levels of 150/100 mmHg post-antibiotic therapy and antihypertensives. New-onset seizures and altered mental status.

Patient Data

Age: 2 years
Gender: Female

In the cuneus of the occipital cortex, there is heterogeneous signal intensity, predominantly demonstrating low signal on T1 and high signal on T2/FLAIR, without diffusion restriction.

There is a susceptibility artifact on SWI with cortical and subcortical involvement. On post-contrast images, there is significant gyriform enhancement, which extends from the tentorium to the inferior parietal lobes.

Case Discussion

Children with posterior reversible encephalopathy syndrome typically present with a sudden onset of neurological symptoms, such as seizures, visual disturbances, headaches, and altered mental status. Focal or generalized seizures are the most common symptom, accounting for approximately 90% of children with PRES.

Posterior reversible encephalopathy syndrome is a complex clinical-radiological syndrome characterized by acute neurological symptoms such as seizures and potentially reversible parieto-occipital vasogenic edema in brain MRI. It is caused by cerebral endotheliopathy with subsequent disruption of vasogenic edema. It occurs in specific settings such as abrupt hypertension, renal disorders, the use of immunosuppressive drugs, or following organ transplantation. Brain MRI is crucial for diagnosing PRES, but validated diagnostic criteria have yet to be established. If the underlying cause is removed in the early phase.

How to use cases

You can use Radiopaedia cases in a variety of ways to help you learn and teach.

Creating your own cases is easy.

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.