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Posterior Reversible Encephalopathy Syndrome in the Postpartum Period: A Rare Entity With Atypical Presentation.

Auriane Leslie Kouam Djembi, Marie-Anne Labaisse, Thibault Warlop, Valery Bogne Kamdem

Cureus April 1, 2025 DOI: 10.7759/cureus.82728 via PubMed

Summary

AI-generated from the abstract

Posterior reversible encephalopathy syndrome (PRES) is a rare brain condition that can occur after childbirth, even in women with normal blood pressure. A case is reported of a first-time mother who developed severe neurological symptoms, including temporary blindness and memory loss, after delivery. Brain imaging showed swelling in unusual areas such as the temporal lobes, hippocampi, and thalami. Special MRI techniques helped distinguish PRES from early stroke, which is critical for proper treatment. The case demonstrates that PRES should be considered in postpartum patients with serious neurological symptoms, regardless of blood pressure or protein levels. Early recognition is important because the syndrome is reversible with timely care.

Study at a glance

Characteristics Case study Case report Peer reviewed
Sample size 1
Population Primiparous patient in the postpartum period
Keywords Diffusion-weighted image dwi Neurologic disorder Postpartum preeclampsia Preeclampsia-eclampsia Postpartum neurological disorders
Citations 1
Key finding PRES can occur in normotensive postpartum patients, presenting with severe neurological symptoms and atypical brain lesions, and can be distinguished from early cerebral ischemia using DWI and ADC MRI mapping.

Abstract

Posterior reversible encephalopathy syndrome (PRES) is a rare condition characterized by clinical and brain imaging criteria. It is most often associated with pregnancy in the postpartum period and has a higher incidence in primiparous patients. Its presentation includes headaches, altered consciousness, seizures, visual disturbances, and specific radiological signs, particularly vasogenic edema of the subcortical white matter, primarily located in the posterior cerebral hemispheres. While PRES in obstetrics is most commonly associated with preeclampsia or, more frequently, eclampsia, we report a case occurring in a normotensive patient. Our case involves a primiparous patient in the postpartum period who presented with a wide range of severe neurological symptoms, including transient cortical blindness and severe memory loss correlated to lesions in atypical regions, such as the temporal lobes and bilateral hippocampi and thalami. The distribution of lesions, the apparent diffusion coefficient (ADC) and diffusion-weighted imaging (DWI) MRI mapping allowed a differentiation of PRES from early cerebral ischemia, thus playing an essential role in management. This case highlights the need to consider PRES in postpartum patients with significant neurological symptoms, regardless of blood pressure or proteinuria status. Early recognition and diagnosis are essential for optimal outcomes, given the reversible nature of the syndrome with timely intervention.

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