Butt Sabeeh-Ur-Rehman, McNeil Julian
Department of Medicine, Lyell McEwin Hospital, Elizabeth Vale, SA, 5112, Australia.
Present Address: Ballarat Base Hospital, Drummond Street North, Ballarat Central, VIC, 3350, Australia.
J Med Case Rep. 2016 Apr 19;10:102. doi: 10.1186/s13256-016-0890-y.
Behçet's disease is a progressive diffuse inflammatory vasculitis characterized by recurrent oral and genital ulceration and ocular inflammation. Cardiac involvement is a rare but well-documented manifestation of Behçet's disease. Complete heart block in non-Caucasian populations has been reported previously; however, in this report, we describe a unique case of complete heart block in a Caucasian woman with Behçet's disease.
A 48-year-old Caucasian woman presented to our hospital with symptomatic complete heart block requiring a pacemaker implant on a background of recurrent oral and genital ulcers and oligoarthritis of 10 months' duration. She also had a history of recurrent diarrhea with a single episode of ocular inflammation in the recent past. She had no evidence of cardiac ischemia, and her autoimmune antibodies were within normal ranges. She was diagnosed with Behçet's disease according to international study group criteria and was commenced on prednisolone and sulfasalazine, to which she responded very well.
Cardiac complications should be considered when making a diagnosis of Behçet's disease, even in Caucasian patients. While mucocutaneous ulceration is indeed the most common manifestation of Behçet's disease, cardiovascular involvement tends to cause the most morbidity and mortality.
白塞病是一种进行性弥漫性血管炎,其特征为复发性口腔和生殖器溃疡以及眼部炎症。心脏受累是白塞病一种罕见但有充分文献记载的表现。此前已有非白种人群发生完全性心脏传导阻滞的报道;然而,在本报告中,我们描述了一例患白塞病的白种女性发生完全性心脏传导阻滞的独特病例。
一名48岁的白种女性因有症状的完全性心脏传导阻滞入住我院,需要植入起搏器,其背景是有持续10个月的复发性口腔和生殖器溃疡以及少关节炎。她近期还有复发性腹泻病史及单次眼部炎症发作史。她没有心脏缺血的证据,自身免疫抗体在正常范围内。根据国际研究组标准,她被诊断为白塞病,并开始使用泼尼松龙和柳氮磺胺吡啶治疗,她对此反应良好。
即使在白种患者中,诊断白塞病时也应考虑心脏并发症。虽然黏膜皮肤溃疡确实是白塞病最常见的表现,但心血管受累往往导致最高的发病率和死亡率。