Patterns of Magnetic Resonance Imaging Abnormalities in Symptomatic Patients With Krabbe Disease Correspond to Phenotype

被引:49
作者
Abdelhalim, Ahmed N. [1 ]
Alberico, Ronald A. [2 ]
Barczykowski, Amy L. [2 ]
Duffner, Patricia K. [3 ]
机构
[1] Roswell Pk Canc Inst, Dept Neuroradiol, Buffalo, NY 14263 USA
[2] SUNY Buffalo, Populat Hlth Observ, Dept Biostat, Buffalo, NY USA
[3] SUNY Buffalo, Sch Med, Hunter James Kelly Res Inst, Dept Neurol, Buffalo, NY 14203 USA
关键词
Krabbe disease; MRI; magnetic resonance imaging; Krabbe phenotypes; age-related findings; GLOBOID-CELL LEUKODYSTROPHY; CORTICOSPINAL TRACT INVOLVEMENT; OPTIC-NERVE ENLARGEMENT; PROTON MR SPECTROSCOPY; EARLY-ONSET; SCORING METHOD; INFANTILE; REGISTRY;
D O I
10.1016/j.pediatrneurol.2013.10.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Initial magnetic resonance imaging studies of individuals with Krabbe disease were analyzed to determine whether the pattern of abnormalities corresponded to the phenotype. METHODS: This was a retrospective, nonblinded study. Families/patients diagnosed with Krabbe disease submitted medical records and magnetic resonance imaging discs for central review. Institutional review board approval/informed consents were obtained. Sixty-four magnetic resonance imaging scans were reviewed by two neuroradiologists and a child neurologist according to phenotype: early infantile (onset 0-6 months) = 39 patients; late infantile (onset 712 months) = 10 patients; later onset (onset 13 months-10 years) = 11 patients; adolescent (onset 1120 years) = one patient; and adult (21 years or greater) = three patients. Local interpretations were compared with central review. RESULTS: Magnetic resonance imaging abnormalities differed among phenotypes. Early infantile patients had a predominance of increased intensity in the dentate/cerebellar white matter as well as changes in the deep cerebral white matter. Later onset patients did not demonstrate involvement in the dentate/cerebellar white matter but had extensive involvement of the deep cerebral white matter, parieto-occipital region, and posterior corpus callosum. Late infantile patients exhibited a mixed pattern; 40% had dentate/cerebellar white matter involvement while all had involvement of the deep cerebral white matter. Adolescent/adult patients demonstrated isolated corticospinal tract involvement. Local and central reviews primarily differed in interpretation of the early infantile phenotype. CONCLUSION: Analysis of magnetic resonance imaging in a large cohort of symptomatic patients with Krabbe disease demonstrated imaging abnormalities correspond to specific phenotypes. Knowledge of these patterns along with typical clinical signs/symptoms should promote earlier diagnosis and facilitate treatment.
引用
收藏
页码:127 / 134
页数:8
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