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7 Tesla MRI of Balo's concentric sclerosis versus multiple sclerosis lesions.
Behrens, Janina R; Wanner, Julia; Kuchling, Joseph; Ostendorf, Lennard; Harms, Lutz; Ruprecht, Klemens; Niendorf, Thoralf; Jarius, Sven; Wildemann, Brigitte; Gieß, René M; Scheel, Michael; Bellmann-Strobl, Judith; Wuerfel, Jens; Paul, Friedemann; Sinnecker, Tim.
Affiliation
  • Behrens JR; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health NeuroCure Cluster of Excellence NeuroCure Clinical Research Center Berlin Germany.
  • Wanner J; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Department of Neurology Humboldt-Universität zu Berlin, and Berlin Institute of Health Berlin Germany.
  • Kuchling J; Berlin Institute of Health Berlin Germany.
  • Ostendorf L; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health NeuroCure Cluster of Excellence NeuroCure Clinical Research Center Berlin Germany.
  • Harms L; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Department of Neurology Humboldt-Universität zu Berlin, and Berlin Institute of Health Berlin Germany.
  • Ruprecht K; Berlin Institute of Health Berlin Germany.
  • Niendorf T; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health NeuroCure Cluster of Excellence NeuroCure Clinical Research Center Berlin Germany.
  • Jarius S; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Department of Neurology Humboldt-Universität zu Berlin, and Berlin Institute of Health Berlin Germany.
  • Wildemann B; Berlin Institute of Health Berlin Germany.
  • Gieß RM; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health NeuroCure Cluster of Excellence NeuroCure Clinical Research Center Berlin Germany.
  • Scheel M; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Department of Neurology Humboldt-Universität zu Berlin, and Berlin Institute of Health Berlin Germany.
  • Bellmann-Strobl J; Berlin Institute of Health Berlin Germany.
  • Wuerfel J; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin Department of Neurology Humboldt-Universität zu Berlin, and Berlin Institute of Health Berlin Germany.
  • Paul F; Clinical and Experimental Multiple Sclerosis Research Center Charite - Universitätsmedizin Berlin Berlin Germany.
  • Sinnecker T; Charité - Universitätsmedizin Berlin Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health NeuroCure Cluster of Excellence NeuroCure Clinical Research Center Berlin Germany.
Ann Clin Transl Neurol ; 5(8): 900-912, 2018 Aug.
Article in En | MEDLINE | ID: mdl-30128315
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 T1-weighted (T1w) magnetization-prepared rapid gradient echo, 2D high spatial resolution T2*-weighted (T2*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 T2*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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Clin Transl Neurol Year: 2018 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Clin Transl Neurol Year: 2018 Type: Article