Patrick Eisenberg Austin, Pearce Brenden, Anders Casey, Collier Victor
Internal Medicine, Grand Strand Medical Center, Myrtle Beach, USA.
Cureus. 2024 Jul 9;16(7):e64159. doi: 10.7759/cureus.64159. eCollection 2024 Jul.
Behcet's disease (BD) is a variable-vessel vasculitis commonly presenting in early adulthood with painful oral aphthous ulcers, genital ulcers, uveitis, pathergy, and skin lesions. The diagnosis of BD is made clinically based on criteria from the International Study Group (ISG) and the International Criteria for Behcet's Disease (ICBD). Due to the wide constellation of symptoms BD can cause, it can be challenging to diagnose in an acute setting. Here, we discuss a patient who presented with a clinical picture of sepsis, with profound ulcerated vulvar and herpetiform oral mucosal lesions, that led us to a presumptive diagnosis of Behcet's disease.
白塞病(BD)是一种累及多系统的血管炎,常见于成年早期,表现为疼痛性口腔溃疡、生殖器溃疡、葡萄膜炎、针刺反应及皮肤损害。BD的诊断基于国际研究组(ISG)标准及国际白塞病诊断标准(ICBD)进行临床诊断。由于BD可引发多种症状,在急性期诊断具有挑战性。在此,我们讨论一位表现为脓毒症临床症状的患者,其有严重的外阴溃疡及疱疹样口腔黏膜损害,这使我们初步诊断为白塞病。