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7 Tesla MRI of Balo's concentric sclerosis versus multiple sclerosis lesions

Authors :
Behrens, J.R.
Wanner, J.
Kuchling, J.
Ostendorf, L.
Harms, L.
Ruprecht, K.
Niendorf, T.
Jarius, S.
Wildemann, B.
Gieß, R.M.
Scheel, M.
Bellmann-Strobl, J.
Wuerfel, J.
Paul, F.
Sinnecker, T.
Source :
Annals of Clinical and Translational Neurology
Publication Year :
2018
Publisher :
John Wiley and Sons Inc., 2018.

Abstract

BACKGROUND: Baló's concentric sclerosis (BCS) is a rare condition characterized by concentrically layered white matter lesions. While its pathogenesis is unknown, hypoxia-induced tissue injury and chemotactic stimuli have been proposed as potential causes of BCS lesion formation. BCS has been suggested to be a variant of multiple sclerosis (MS). Here, we aimed to elucidate similarities and differences between BCS and MS by describing lesion morphology and localization in high-resolution 7 Tesla (7 T) magnetic resonance imaging (MRI) scans. METHODS: Ten patients with Baló-type lesions underwent 7 T MRI, and 10 relapsing remitting MS patients served as controls. The 7 T MR imaging protocol included 3D T(1)-weighted (T(1)w) magnetization-prepared rapid gradient echo, 2D high spatial resolution T(2)*-weighted (T(2)*w) fast low-angle shot and susceptibility-weighted imaging. RESULTS: Intralesional veins were visible in the center of all but one Baló-type lesion. Four Baló-type lesions displayed inhomogeneous intralesional T(2)*w signal intensities, which are suggestive of microhemorrhages or small ectatic venules. Eight of 10 BCS patients presented with 97 additional lesions, 36 of which (37%) had a central vein. Lesions involving the cortical gray matter and the U-fibers were not detected in BCS patients. CONCLUSION: Our findings support the hypothesis that BCS and MS share common pathogenetic mechanisms but patients present with different lesion phenotypes.

Details

Language :
English
ISSN :
23289503
Volume :
5
Issue :
8
Database :
OpenAIRE
Journal :
Annals of Clinical and Translational Neurology
Accession number :
edsair.doi.dedup.....9aa4c252d2cde518ffb0884cec2a8280