Reversible Posterior Leukoencephalopathy Syndrome in Children: MR Imaging Findings.
10.3348/jkrs.2001.44.2.249
- Author:
Sang Kwon LEE
1
;
Soon Hak KWON
;
Yong Sun KIM
Author Information
1. Department of Radiology, College of Medicine, Kyungpook National University.
- Publication Type:Original Article
- Keywords:
Brain,disease;
Brain, MR;
Magnetic resonance (MR), in infants and children
- MeSH:
Basal Ganglia;
Brain;
Cerebellum;
Child*;
Cyclosporine;
Follow-Up Studies;
Frontal Lobe;
Ganglioneuroma;
Hemolytic-Uremic Syndrome;
Hemorrhage;
Humans;
Hypertension;
Lactic Acid;
Magnetic Resonance Imaging*;
Magnetic Resonance Spectroscopy;
Paraganglioma;
Parietal Lobe;
Posterior Leukoencephalopathy Syndrome*;
Protons;
Rabeprazole;
Retrospective Studies
- From:Journal of the Korean Radiological Society
2001;44(2):249-256
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: To find out the characteristic MR findings of reversible posterior leukoen-cephalopathy syndrome (RPLS) due to various causes in children. MATERIALS AND METHODS: Eight children with RPLS underwent MR imaging, and the findings were retrospectively analyzed. All eight were acutely hypertensive at the time of a neurotoxic episode. Three had intra-abdominal tumors (one adrenal pheochromo-cytoma, one para-aortic paraganglioma and one para-aortic ganglioneuroma encasing the left renal artery); three were being treated with cyclosporine; one was being treat-ed with steroid; and one had hemolytic uremic syndrome. Initial cranial MR images were analyzed with particular emphasis on the distribution of the lesions. To assess possible sequelae, follow-up MR images were obtained in seven patients at least one week after the treatment of hypertension. Four underwent proton MR spectroscopy. RESULTS: Characteristic distribution of lesions in the occipital and posterior parietal lobes was identified in all cases regardless of the causes of RPLS. The cerebellum, basal ganglia, anterior parietal, and frontal lobe were involved in four, two, one, and one case, respectively. Cortical gray matter involvement was predominant in six and subcortical white matter involvement predominated in two patients. The distribution of lesions was bilateral and asymmetric. Gyriform enhancement was identified in six cases, and small hemorrhage was noted in one. In seven patients, the clinical and MR findings improved without sequelae on follow-up study. In one, proton MR spectroscopy demonstrated a high lactate peak at the time of the neurologic event. Nearnormal spectra were noted in three children who underwent proton MR spectroscopy after recovery. CONCLUSION: The MR findings of RPLS are characteristic in that lesions are distributed in the posterior region of the brain and they are reversible on follow-up study. In children with RPLS due to unknown causes, the possibility of intra-abdominal tumors should also be considered.
