| Title | Indications for Magnetic Resonance Imaging in Patients With Behcet Uveitis |
| Creator | Anna Borelli; Jordan Behr; Maria Ruggeri; Mini Han; Yujia Zhou; C. Stephen Foster |
| Affiliation | Massachusetts Eye Research and Surgery Institution (AB, JB, MR, MH, YZ, CSF), Waltham, Massachusetts; The Ocular Immunology and Uveitis Foundation (AB, JB, MR, MH, YZ, CSF), Waltham, Massachusetts; and Department of Ophthalmology (CSF), Harvard Medical School, Boston, Massachusetts |
| Abstract | Background: Behcet disease is a systemic vasculitis, which may involve the eyes and central nervous system. The true prevalence of neurological involvement is not precisely known but may be associated with ocular involvement. This study investigates the association between Behcet uveitis and neuro-Behcet disease. Methods: A retrospective single-center analysis was conducted for consecutive patients with Behcet uveitis at the Massachusetts Eye Research and Surgery Institution. Uveitis characteristics, neurological symptoms, fluorescein fundus angiography, and MRI results were recorded. Results: Our population included 108 patients with Behcet uveitis, and 26 (24.1%) were found to have neurological involvement associated with Behcet disease. Optic nerve leakage on fundus angiography and neurological symptoms were associated with an increased risk of neurological involvement. Three cases (11.5%) were nonparenchymal, while 23 (88.5%) were parenchymal with lesions in the cortex, subcortical white matter, thalamus, basal ganglia, and brainstem. Conclusions: There is a high comorbidity between ocular and neurological involvement in Behcet disease. Careful assessment of neurological symptoms and baseline fluorescein fundus angiography are recommended for patients with Behcet disease. MRI has a high diagnostic yield and should be pursued if there is concern for progressive or pre-existing neurological involvement. |
| Subject | Adult; Behcet Syndrome / complications; Behcet Syndrome / diagnosis; Female; Fluorescein Angiography; Humans; Magnetic Resonance Imaging / methods; Male; Middle Aged; Retrospective Studies; Uveitis / diagnosis; Uveitis / etiology; Young Adult |
| Date | 2024-12 |
| Date Digital | 2024-12 |
| References | Behcet's Disease Research Committee of Japan. Behçet's disease: guide to diagnosis of Behçet's disease. Jpn J Ophthalmol. 1974;18:291-294. Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease. Lancet. 1990;335:1078-1080.Davatchi F, Assaad-Khalil S, Calamia KT, et al. The International Criteria for Behçet's Disease (ICBD): a collaborative study of 27 countries on the sensitivity and specificity of the new criteria. J Eur Acad Dermatol Venereol. 2014;28:338-347. Yazici H, Seyahi E, Hatemi G, Yazici Y. Behçet syndrome: a contemporary view. Nat Rev Rheumatol. 2018;14:107-119. Borhani-Haghighi A, Kardeh B, Banerjee S, et al. Neuro-Behcet's disease: an update on diagnosis, differential diagnoses, and treatment. Mult Scler Relat Disord. 2020;39:101906. |
| Language | eng |
| Format | application/pdf |
| Type | Text |
| Publication Type | Journal Article |
| Source | Journal of Neuro-Ophthalmology, December 2024, Volume; 44, Issue 4 |
| Collection | Neuro-Ophthalmology Virtual Education Library: Journal of Neuro-Ophthalmology Archives: https://novel.utah.edu/jno/ |
| Publisher | Lippincott, Williams & Wilkins |
| Holding Institution | Spencer S. Eccles Health Sciences Library, University of Utah |
| Rights Management | © North American Neuro-Ophthalmology Society |
| ARK | ark:/87278/s6wa438k |
| Setname | ehsl_novel_jno |
| ID | 2932959 |
| Reference URL | https://collections.lib.utah.edu/ark:/87278/s6wa438k |