Korean J Cerebrovasc Surg.
2004 Sep;6(2):177-180.
Posterior Reversible Encephalopathy Syndrome in Eclamptic Encephalopathy: A Case Report
- Affiliations
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- 1Department of Emergency Medicine, Gachon Medical School, Incheon, Korea. yanghj@gachon.ac.kr
- 2Department of Diagnostic Radiology, Gachon Medical School, Incheon, Korea.
- 3Department of Neurosurgery, Gil Medical Center, Gachon Medical School, Incheon, Korea.
Abstract
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Posterior reversible encephalopathy syndrome (PRES) is characterized by headache, vomiting, confusion, and seizure. In addition, PRES is associated with reversible bilateral cortical and subcortical edema on occipital lobe or parieto-occipital lobe. Eclampsia is a rare condition to pregnant and puerperal women and one of common causes of the PRES. The clinical and radiologic manifestations can be resolved without irreversible complication by early diagnosis and appropriate treatment. The authors report a case of eclamptic encephalopathy associated with PRES, in which an 18-year-old woman had clinical manifestations of visual disturbance, headache, and tonic-clonic seizure at 34 hours after vaginal delivery. High signal intensities are seen in both parieto-occipital lobes and left basal ganglia on fluid attenuated inversion recovery (FLAIR) images and T2 weighted images performed at emergency room. But no significant signal change in both parieto-occipital lobes on diffusion weighted images (DWI). Because seizure was repeated, then anticonvulsant was administered at intensive care unit. On the second day, the clinical manifestations were resolved as blood pressure was normalized. The FLAIR imaging and DWI sequences can play an important role in the diagnosis of PRES.