Delayed posthypoxic demyelination - Association with arylsulfatase A deficiency and lactic acidosis on proton MR spectroscopy

被引:60
作者
Gottfried, JA
Mayer, SA
Shungu, DC
Chang, Y
Duyn, JH
机构
[1] NYU, MED CTR, DEPT PHYSIOL, NEW YORK, NY 10016 USA
[2] NYU, MED CTR, DEPT NEUROSCI, NEW YORK, NY 10016 USA
[3] COLUMBIA PRESBYTERIAN MED CTR, DEPT NEUROL, NEW YORK, NY 10032 USA
[4] COLUMBIA PRESBYTERIAN MED CTR, DEPT RADIOL, NEW YORK, NY 10032 USA
[5] COLUMBIA PRESBYTERIAN MED CTR, DEPT PATHOL, NEW YORK, NY 10032 USA
[6] NIH, LAB DIAGNOST RADIOL RES, BETHESDA, MD 20892 USA
关键词
D O I
10.1212/WNL.49.5.1400
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Delayed demyelination is a rare and poorly understood complication of hypoxic brain injury. A previous case report has suggested an association with mild-to-moderate deficiency of arylsulfatase A. We describe a 36-year-old man who recovered completely from an episode of hypoxia related to drug overdose, and 2 weeks later progressed from a confusional state to deep coma. MRI showed diffuse white matter signal changes, and brain biopsy demonstrated a noninflammatory demyelinating process. Proton magnetic resonance spectroscopy revealed elevated choline and lactate and reduced N-acetyl aspartate signal in the affected white matter, consistent with demyelination and a shift to anaerobic metabolism. Arylsulfatase A activity from peripheral leukocytes was approximately 50% of normal, consistent with a ''pseudodeficiency'' phenotype. These findings confirm the hypothesis that relative arylsulfatase A deficiency predisposes susceptible individuals to delayed posthypoxic leukoencephalopathy and implicates lactic acidosis in the pathogenesis of this disorder.
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页码:1400 / 1404
页数:5
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