Posterior Leukoencephalopathy Syndrome in Children and Adolescents

Author:

Alehan Füsun1,Erol Ilknur2,Agildere A. Muhtesem3,Ozcay Figen4,Baskin Esra5,Cengiz Nurcan5,Alioglu Bülent6,Haberal Mehmet7

Affiliation:

1. Pediatrics (Divisions of Neurology), Başkent University of Medicine Ankara, Turkey

2. Pediatrics (Divisions of Neurology), Başkent University of Medicine Ankara, Turkey,

3. Departments of Pediatrics (Division of Radiology), Başkent University Faculty of Medicine Ankara, Turkey

4. Pediatric Gastroenterology and Hepatology, Başkent University of Medicine Ankara, Turkey

5. Nephrology, Başkent University Faculty of Medicine Ankara, Turkey

6. Hematology, Başkent University Faculty of Medicine Ankara, Turkey

7. General Surgery, Başkent University Faculty of Medicine Ankara, Turkey

Abstract

Posterior leukoencephalopathy syndrome is a recently identified clinical and radiologic entity. The characteristic radiologic findings are bilateral gray and white matter edema in the posterior regions of the cerebral hemispheres. This article reports clinical and radiologic findings in 10 consecutive episodes of posterior leukoencephalopathy syndrome that were diagnosed in 9 children and adolescents. The causes were immunosuppressive therapy in 7 patients and a combination of renal failure and hypertension in 3. The most common presenting symptoms were seizure and altered consciousness; others included headache, sixth nerve palsy, and cortical blindness. Imaging demonstrated abnormalities in the parietal and occipital lobes in all 10 episodes. The signs and symptoms resolved after immunosuppressive agents were reduced or discontinued, or after uremia and hypertension were corrected. Four patients underwent follow-up cranial imaging, and the images showed nearly complete or complete resolution. The syndrome was clinically reversible in all patients.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

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