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Acute Magnetic Resonance Imaging Findings in Young Children With Moyamoya Disease.

Authors :
Numoto S
Takasu S
Nakamura T
Takagi M
Kurahashi H
Azuma Y
Okumura A
Source :
Pediatric neurology [Pediatr Neurol] 2024 Jul; Vol. 156, pp. 106-112. Date of Electronic Publication: 2024 Apr 03.
Publication Year :
2024

Abstract

Background: To describe the diffusion-weighted imaging (DWI) findings in young children with moyamoya disease (MMD) during the acute period of the condition.<br />Methods: Clinical data were collected from 12 children with MMD aged less than six years, in whom abnormalities were observed on DWI scans obtained within one week after the appearance of symptoms related to MMD. The DWI abnormalities were classified into gyral, atypical territorial, honeycomb, classical territorial, multiple-dot, border zone, and deep lacunar patterns. The severity of arterial stenosis was graded by angiographic stages that have been previously described.<br />Results: In all but one child, the DWI abnormalities were restricted to the cerebral cortex. The lesions were gyral in nature in seven children and atypical territorial in five; all differed from those of typical arterial strokes. Internal carotid artery stenosis was observed in all 12 children, although the stenosis was mild in 11. The severity of arterial stenosis did not match the regions of ischemic lesions in some children. There was no statistically significant difference in the severity of arterial stenosis according to the presence or absence of ischemic lesions or the pattern of the lesions.<br />Conclusions: Lesions located mainly in the cerebral cortex, i.e., not in arterial territories, are characteristic of young children with MMD.<br />Competing Interests: Declaration of competing interest The authors declare no conflicts of interest associated with this manuscript.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-5150
Volume :
156
Database :
MEDLINE
Journal :
Pediatric neurology
Publication Type :
Academic Journal
Accession number :
38749382
Full Text :
https://doi.org/10.1016/j.pediatrneurol.2024.03.025