Alibaz-Oner Fatma, Direskeneli Haner
Division of Rheumatology, School of Medicine, Marmara University, Istanbul, Turkey.
Int J Rheum Dis. 2019 Jan;22 Suppl 1:105-108. doi: 10.1111/1756-185X.13298. Epub 2018 Apr 17.
Behçet's disease (BD) is a chronic, multisystemic, inflammatory disease characterized by recurrent attacks of mucocutaneous, ocular, musculoskeletal, vascular, central nervous system and gastrointestinal manifestations. Treatment of BD changes according to organ involvement, gender and age of the patient with no golden standard therapeutic regimen. Vascular involvement is observed in up to 40% of the patients with BD, especially in young males and is one of the major causes of mortality and morbidity. Glucocorticoids, azathioprine and cyclophosphamide are still recommended as the first-line treatments in vascular BD. However, increasing data with the tumor necrosis factor inhibitors suggest that these agents may also be acceptable options for the management of refractory vascular BD in daily practice. Anticoagulant usage for vascular BD is also still controversial with limited data coming from retrospective studies. There is a clear need for randomized, controlled studies for the management of VBD.
白塞病(BD)是一种慢性、多系统炎症性疾病,其特征为黏膜皮肤、眼部、肌肉骨骼、血管、中枢神经系统和胃肠道反复出现症状。BD的治疗方案会根据患者的器官受累情况、性别和年龄而有所不同,目前尚无金标准治疗方案。高达40%的BD患者会出现血管受累,尤其是年轻男性,这是导致死亡和发病的主要原因之一。糖皮质激素、硫唑嘌呤和环磷酰胺仍被推荐为血管型BD的一线治疗药物。然而,越来越多关于肿瘤坏死因子抑制剂的数据表明,在日常实践中,这些药物也可能是治疗难治性血管型BD的可接受选择。血管型BD使用抗凝剂也仍存在争议,回顾性研究的数据有限。显然需要进行随机对照研究来管理血管型BD。