Elmassry Marawan, Matar Sayed, Thongpiya Jerapas, Yingchoncharoen Pitchaporn, Abohelwa Mostafa, Islam Sameer
Department of Internal Medicine Texas Tech university Health Sciences Centre Lubbock Texas USA.
Department of Pathology Brigham and Women Hospital, Harvard Medical School Boston Massachusetts USA.
Clin Case Rep. 2023 May 18;11(5):e7359. doi: 10.1002/ccr3.7359. eCollection 2023 May.
Behçet's disease (BD) or syndrome is a chronic, recurrent, multisystem, inflammatory vasculitis disorder with findings of oral aphthous ulcers, genital ulcers, and uveitis. Gastrointestinal (GI) involvement can be the initial presentation as presented in this case.
Behçet's disease (BD) or syndrome is a chronic, recurrent, multisystem, inflammatory vasculitis disorder of unknown etiology with classical findings of oral aphthous ulcers, genital ulcers, and ocular involvements including chronic anterior, intermediate, posterior, and even panuveitis. Gastrointestinal involvement in BD usually presents with chronic diarrhea, hematochezia as the disease affects ileocecal area which might be similar to presentation of inflammatory bowel diseases. Here, we report a case of undiagnosed BD who presented with chronic diarrhea for 4 months, leading to the diagnosis of BD and responded well to corticosteroid therapy.
白塞病(BD)或白塞综合征是一种慢性、复发性、多系统炎症性血管炎疾病,表现为口腔阿弗他溃疡、生殖器溃疡和葡萄膜炎。胃肠道受累可能是如本病例所示的首发表现。
白塞病(BD)或白塞综合征是一种病因不明的慢性、复发性、多系统炎症性血管炎疾病,具有口腔阿弗他溃疡、生殖器溃疡以及眼部受累(包括慢性前葡萄膜炎、中间葡萄膜炎、后葡萄膜炎甚至全葡萄膜炎)等典型表现。白塞病的胃肠道受累通常表现为慢性腹泻、便血,因为该病累及回盲部,这可能与炎症性肠病的表现相似。在此,我们报告一例未确诊的白塞病患者,该患者出现慢性腹泻4个月,最终诊断为白塞病,且对皮质类固醇治疗反应良好。