Literature DB >> 11979570

Quantitative MRI assessment of leukoencephalopathy.

Wilburn E Reddick1, John O Glass, James W Langston, Kathleen J Helton.   

Abstract

Quantitative MRI assessment of leukoencephalopathy is difficult because the MRI properties of leukoencephalopathy significantly overlap those of normal tissue. This report describes the use of an automated procedure for longitudinal measurement of tissue volume and relaxation times to quantify leukoencephalopathy. Images derived by using this procedure in patients undergoing therapy for acute lymphoblastic leukemia (ALL) are presented. Five examinations from each of five volunteers (25 examinations) were used to test the reproducibility of quantitated baseline and subsequent, normal-appearing images; the coefficients of variation were less than 2% for gray and white matter. Regions of leukoencephalopathy in patients were assessed by comparison with manual segmentation. Two radiologists manually segmented images from 15 randomly chosen MRI examinations that exhibited leukoencephalopathy. Kappa analyses showed that the two radiologists' interpretations were concordant (kappa = 0.70) and that each radiologist's interpretations agreed with the results of the automated procedure (kappa = 0.57 and 0.55). The clinical application of this method was illustrated by analysis of images from sequential MR examinations of two patients who developed leukoencephalopathy during treatment for ALL. The ultimate goal is to use these quantitative MR imaging measures to better understand therapy-induced neurotoxicity, which can be limited or even reversed with some combination of therapy adjustments and pharmacological and neurobehavioral interventions. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 11979570      PMCID: PMC2396564          DOI: 10.1002/mrm.10124

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  23 in total

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2.  Parameter estimation and tissue segmentation from multispectral MR images.

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3.  Acute neurotoxicity in children with B-precursor acute lymphoid leukemia: an association with intermediate-dose intravenous methotrexate and intrathecal triple therapy--a Pediatric Oncology Group study.

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4.  Automated segmentation and classification of multispectral magnetic resonance images of brain using artificial neural networks.

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Journal:  IEEE Trans Med Imaging       Date:  1997-12       Impact factor: 10.048

5.  Correspondence of closest gradient voxels--a robust registration algorithm.

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Journal:  J Magn Reson Imaging       Date:  1997 Mar-Apr       Impact factor: 4.813

6.  Conventional compared with individualized chemotherapy for childhood acute lymphoblastic leukemia.

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7.  Improved intracranial lesion characterization by tissue segmentation based on a 3D feature map.

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8.  Age-related changes in proton T1 values of normal human brain.

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9.  Multiple sclerosis lesion quantification using fuzzy-connectedness principles.

Authors:  J K Udupa; L Wei; S Samarasekera; Y Miki; M A van Buchem; R I Grossman
Journal:  IEEE Trans Med Imaging       Date:  1997-10       Impact factor: 10.048

10.  Intellectual function in long-term survivors of childhood acute lymphoblastic leukemia: protective effect of pre-irradiation methotrexate? A Childrens Cancer Study Group study.

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  13 in total

1.  The relationship between working memory and cerebral white matter volume in survivors of childhood brain tumors treated with conformal radiation therapy.

Authors:  Lisa M Jacola; Jason M Ashford; Wilburn E Reddick; John O Glass; Robert J Ogg; Thomas E Merchant; Heather M Conklin
Journal:  J Neurooncol       Date:  2014-05-22       Impact factor: 4.130

2.  Attention and working memory abilities in children treated for acute lymphoblastic leukemia.

Authors:  Jason Ashford; Corrie Schoffstall; Wilburn E Reddick; Christina Leone; Fred H Laningham; John O Glass; Deqing Pei; Cheng Cheng; Ching-Hon Pui; Heather M Conklin
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3.  A quantitative MR imaging assessment of leukoencephalopathy in children treated for acute lymphoblastic leukemia without irradiation.

Authors:  Wilburn E Reddick; John O Glass; Kathleen J Helton; James W Langston; Chin-Shang Li; Ching-Hon Pui
Journal:  AJNR Am J Neuroradiol       Date:  2005-10       Impact factor: 3.825

4.  Brain volume in pediatric patients with sickle cell disease: evidence of volumetric growth delay?

Authors:  R Grant Steen; Temitope Emudianughe; Michael Hunte; John Glass; Shengjie Wu; Xiaoping Xiong; Wilburn E Reddick
Journal:  AJNR Am J Neuroradiol       Date:  2005-03       Impact factor: 3.825

5.  Improving the segmentation of therapy-induced leukoencephalopathy in children with acute lymphoblastic leukemia using a priori information and a gradient magnitude threshold.

Authors:  John O Glass; Wilburn E Reddick; Cara Reeves; Ching-Hon Pui
Journal:  Magn Reson Med       Date:  2004-12       Impact factor: 4.668

Review 6.  Prevalence of leukoencephalopathy in children treated for acute lymphoblastic leukemia with high-dose methotrexate.

Authors:  Wilburn E Reddick; John O Glass; Kathleen J Helton; James W Langston; Xiaoping Xiong; Shengjie Wu; Ching-Hon Pui
Journal:  AJNR Am J Neuroradiol       Date:  2005-05       Impact factor: 3.825

7.  Evaluation of memory impairment in aging adult survivors of childhood acute lymphoblastic leukemia treated with cranial radiotherapy.

Authors:  Gregory T Armstrong; Wilburn E Reddick; Ronald C Petersen; Aimee Santucci; Nan Zhang; Deokumar Srivastava; Robert J Ogg; Claudia M Hillenbrand; Noah Sabin; Matthew J Krasin; Larry Kun; Ching-Hon Pui; Melissa M Hudson; Leslie L Robison; Kevin R Krull
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8.  Regional brain glucose metabolism and neurocognitive function in adult survivors of childhood cancer treated with cranial radiation.

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Review 9.  Quantitative morphologic evaluation of magnetic resonance imaging during and after treatment of childhood leukemia.

Authors:  Wilburn E Reddick; Fred H Laningham; John O Glass; Ching-Hon Pui
Journal:  Neuroradiology       Date:  2007-07-26       Impact factor: 2.804

10.  Cerebellocerebral diaschisis is the likely mechanism of postsurgical posterior fossa syndrome in pediatric patients with midline cerebellar tumors.

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