Clinical Characteristics, MRI Findings, Disease Progression, and Management of Neuro-Behçet’s Disease: A Retrospective Study in Lebanon
Nadia Chamoun, Martine Elbejjani, Nabil K. El Ayoubi, Taha Hatab, Dana Hazimeh, Michael Ibrahim, Mira Merashli

TL;DR
This study examines the clinical features, MRI findings, and treatment outcomes of Neuro-Behçet’s Disease in a Middle Eastern population.
Contribution
The study provides new insights into the prevalence and management of Neuro-Behçet’s Disease in Lebanon.
Findings
Neuro-Behçet’s Disease affected 10.3% of Behçet’s Disease patients in the study cohort.
Female patients with parenchymal NBD had more severe disease progression compared to males.
Corticosteroids and colchicine were the most commonly used treatments for NBD.
Abstract
Background: Behçet’s Disease (BD) is a complex vasculitis affecting multiple organ systems, with Neuro-Behçet’s Disease (NBD) representing a rare yet severe manifestation. Data on NBD are limited, particularly in Middle Eastern populations. Methods: This retrospective observational study, spanning from 2000 to 2021, involved 262 BD patients at a tertiary medical center in Lebanon. NBD was diagnosed based on International Consensus Recommendation diagnostic criteria. Clinical data, including demographics, manifestations, inflammatory blood markers, genetics, and treatments, were collected. The modified Rankin Scale (mRS) was used to assess disease severity. Results: Among the cohort, 27 (10.3%) had NBD, with headaches, weakness, and dizziness as the most common presenting symptoms. The prevalence of NBD was similar across genders, which differs from some regional studies. HLA-B51…
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Taxonomy
TopicsOcular Diseases and Behçet’s Syndrome · Systemic Lupus Erythematosus Research · Retinal and Optic Conditions
