Pediatric Neurology
Volume 24, Issue 5 , Pages 361-364, May 2001

Clinical spectrum of reversible posterior leukoencephalopathy syndrome

  • Soonhak Kwon, MD

      Affiliations

    • Department of Pediatrics; Kyungpook National University Hospital; Taegu, South Korea
    • Corresponding Author InformationCommunications addressed to: Dr. Kwon; Department of Pediatrics; Kyungpook National University Hospital; Samdeok 2-50; Joong-Gu; Taegu,700-721, South Korea
  • ,
  • Jahoon Koo, MD

      Affiliations

    • Department of Pediatrics; Kyungpook National University Hospital; Taegu, South Korea
  • ,
  • Sangkwon Lee, MD

      Affiliations

    • Department of Radiology; Kyungpook National University Hospital; Taegu, South Korea

Received 10 October 2000; accepted 14 February 2001.

Abstract 

Reversible posterior leukoencephalopathy syndrome is a recently recognized disorder with characteristic radiologic findings that mainly involve the white/gray matter of the parieto-occipital lobes. This complex syndrome is associated with cyclosporine A therapy or a variety of other conditions in which blood pressure rises acutely. Twelve patients from a variety of conditions who met the diagnostic criteria for this syndrome were studied. Interestingly, three of these patients had intra-abdominal neurogenic tumors, which have rarely been reported. Initial cranial magnetic resonance imaging scans revealed fairly symmetric areas of increased T2 signal involving both white and gray matter of parieto-occipital lobes in the majority of the patients. However, the lesions were often located outside the parieto-occipital regions. Four patients had occipital region magnetic resonance spectroscopy during the acute phase, which revealed high lactate peak and normal N-acetyl aspartate/creatine and choline peaks. With appropriate treatment, most patients recovered from this syndrome and experienced almost complete resolution of brain lesions on follow-up magnetic resonance imaging. One patient, however, continued to have small residual hemosiderin deposits on a follow-up magnetic resonance imaging with neurologic sequellae. In conclusion, a better understanding of this complex syndrome may obviate unnecessary investigations and allow management of the associated problems in prompt and appropriate ways.

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PII: S0887-8994(01)00265-X

Pediatric Neurology
Volume 24, Issue 5 , Pages 361-364, May 2001