Investigating the Frequency and Outcome of Central Vein Sign and Paramagnetic Rim Lesions in Children With MOGAD

医学 放射科 病变 神经组阅片室 符号(数学) 磁共振成像 病理 血管疾病 静脉 外科 回顾性队列研究
作者
Riccardo Nistri,Laura Cacciaguerra,Simone Sacco,Akash Virupakshaiah,Ermelinda De Meo,Nico Papinutto,Roland Henry,Hadas Meirson,Cheryl Hemingway,Dr Thomas Rossor,Evangeline Wassmer,Liat Bensira,Li-tal Pratt,Asthik Biswas,Sniya Sudhakar,Kshitij Mankad,John J. Chen,S J Pittock,Frederik Barkhof,Olga Ciccarelli
出处
期刊:Neurology [Lippincott Williams & Wilkins]
卷期号:106 (3): e214410-e214410 被引量:1
标识
DOI:10.1212/wnl.0000000000214410
摘要

BACKGROUND AND OBJECTIVES: Central vein sign (CVS) is a common feature in multiple sclerosis (MS) lesions, but its frequency in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) varies significantly across studies. Paramagnetic rim lesions (PRLs) are described in MS, but not in MOGAD. Our goals were to evaluate the prevalence of PRLs and CVS in a large multicenter cohort of pediatric MOGAD. We compared CVS frequencies between acute vs remission phases, as well as with longitudinal dynamics of lesion evolution. METHODS: In this longitudinal retrospective multicenter study, clinical MRIs were assessed from pediatric patients with MOGAD, who had (1) ≥1 brain lesion, (2) susceptibility-based imaging (SBI), and (3) follow-up MRI at least 3 months apart. T2-weighted and fluid-attenuated inversion recovery sequences were analyzed for lesion detection and resolution. SBI was used to assess CVS and PRLs following North American Imaging in MS Cooperative criteria. RESULTS: < 0.001). No PRLs were identified. DISCUSSION: Lesion pathobiology in MOGAD is heterogeneous. CVS identified persistent rather than transient lesions, with resolution more common among CVS- lesions. The high frequency of confluent or multivein lesions limited the proportion suitable for CVS analysis. MRI timing influenced CVS detection, which was higher in remission, suggesting that time of acquisition contributes to variability across MOGAD studies. No PRLs were found, supporting their potential as biomarkers distinguishing MOGAD from MS.
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