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- W2087653001 abstract "Behçet syndrome is a multisystemic autoimmune disease with vascular manifestations, oral and genital aphthous ulcers, skin lesions, ocular involvement, and pathergy phenomenon as defined by the 2006 International Criteria for Behçet's Disease, which has been deemed the most sensitive diagnostic criterion. [1] Davatchi F. Diagnosis/classification criteria for Behçet disease. Patholog Res Int. 2012; 2012: 607921 Crossref PubMed Scopus (93) Google Scholar Therapy typically involves immunosuppression aimed at dampening the autoimmune response to the disease with agents such as colchicine, which inhibits neutrophil chemotaxis; disease-modifying compounds, such as azathioprine; the alkylating agent cyclophosphamide; anti–tumor necrosis factor α agents, and surgical intervention for issues such as arterial aneursyms. [2] Alpsoy E. New evidence-based treatment approach in Behçet disease. Patholog Res Int. 2012; 2012: 871019 PubMed Google Scholar Reports exist of patients successfully treated with intravenous immunoglobulin (IVIG) for ocular manifestations of the disease. [3] Seider N. Beiran I. Scharf J. Miller B. Intravenous immunoglobulin therapy for resistant ocular Behçet's disease. Br J Ophthalmol. 2001; 85: 1287-1288 Crossref PubMed Scopus (54) Google Scholar" @default.
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- W2087653001 date "2012-07-01" @default.
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- W2087653001 title "Optimal use of ivig in a patient with Behçet syndrome and common variable immunodeficiency" @default.
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- W2087653001 doi "https://doi.org/10.1016/j.anai.2012.05.014" @default.
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