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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Research ArticlePediatrics

Pediatric Acute Toxic Leukoencephalopathy: Prediction of the Clinical Outcome by FLAIR and DWI for Various Etiologies

K. Ozturk, J. Rykken and A.M. McKinney
American Journal of Neuroradiology August 2020, 41 (8) 1517-1524; DOI: https://doi.org/10.3174/ajnr.A6624
K. Ozturk
aFrom the Department of Radiology, University of Minnesota, Minneapolis, Minnesota.
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J. Rykken
aFrom the Department of Radiology, University of Minnesota, Minneapolis, Minnesota.
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A.M. McKinney
aFrom the Department of Radiology, University of Minnesota, Minneapolis, Minnesota.
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Abstract

BACKGROUND AND PURPOSE: Pediatric acute toxic leukoencephalopathy is a clinicoradiologic entity comprising various etiologies. This study aimed to identify the MR imaging appearance of pediatric acute toxic leukoencephalopathy from various etiologies and determine whether the etiology correlates with clinical outcome.

MATERIALS AND METHODS: We retrospectively reviewed the electronic records of patients with pediatric acute toxic leukoencephalopathy younger than 19 years of age who had MR imaging within <2 weeks of presentation, including DWI and FLAIR sequences. Two neuroradiologists scored the DWI and FLAIR severity and measured the percentage ADC reduction within the visibly affected regions and normal-appearing WM. The percentage ADC reduction and DWI and FLAIR severity were correlated with clinical outcome using the Spearman correlation.

RESULTS: Of 22 children, 3 were excluded due to a nontoxic cause or incomplete examination. Regarding the included 19 children (mean age, 13 years), the etiologies of pediatric acute toxic leukoencephalopathy were the following: methotrexate (n = 6), bone marrow transplantation (n = 4), fludarabine (n = 3), cytarabine (n = 1), carboplatin (n = 1), vincristine (n = 1), cyclosporine (n = 1), uremia (n = 1), and bevacizumab (n = 1). Three subgroups were analyzed (chemotherapy, n = 12; immunosuppression, n = 5; others, n = 2). There was a strong correlation of FLAIR (r = 0.773, P < .001) and DWI (r = 0.851, P < .001) severity with clinical outcome, and patients treated with fludarabine had the worst outcomes. High percentage ADC reduction values were associated with adverse outcomes, and lower percentage ADC reduction values were associated with favorable outcomes (r = 0.570, P = .011).

CONCLUSIONS: The DWI and FLAIR severity scores appear highly prognostic, whereas percentage ADC reduction is moderately prognostic for clinical outcomes in pediatric acute toxic leukoencephalopathy. Immunosuppressive pediatric acute toxic leukoencephalopathy tends toward favorable outcomes, and fludarabine tends toward worse outcomes.

ABBREVIATIONS:

%ADCR
percentage ADC reduction
ATL
acute toxic leukoencephalopathy
BMT
bone marrow transplantation
NAWM
normal-appearing WM
PATL
pediatric acute toxic leukoencephalopathy
PRES
posterior reversible encephalopathy
PVWM
periventricular WM
  • © 2020 by American Journal of Neuroradiology
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American Journal of Neuroradiology: 41 (8)
American Journal of Neuroradiology
Vol. 41, Issue 8
1 Aug 2020
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Cite this article
K. Ozturk, J. Rykken, A.M. McKinney
Pediatric Acute Toxic Leukoencephalopathy: Prediction of the Clinical Outcome by FLAIR and DWI for Various Etiologies
American Journal of Neuroradiology Aug 2020, 41 (8) 1517-1524; DOI: 10.3174/ajnr.A6624

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Pediatric Acute Toxic Leukoencephalopathy: Prediction of the Clinical Outcome by FLAIR and DWI for Various Etiologies
K. Ozturk, J. Rykken, A.M. McKinney
American Journal of Neuroradiology Aug 2020, 41 (8) 1517-1524; DOI: 10.3174/ajnr.A6624
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