Ujaimi Ziyad, Bjursten Henrik, Vucicevic Sanja, Brunnström Hans, Gilje Patrik, Rasmussen Magnus, Ragnarsson Sigurdur
Department of Cardiothoracic Surgery, Lund University, Skåne University Hospital, Lund, Sweden.
Department of Infection Medicine, Kristianstad Hospital, Sweden.
IDCases. 2023 May 18;32:e01800. doi: 10.1016/j.idcr.2023.e01800. eCollection 2023.
Whipple´s disease is a rare multisystem condition affecting < 1/1.000.000 per year. The condition often presents with polyarthritis, diarrhea, and intestinal malabsorption. Endocarditis is seen in a minority of these patients, and is typically culture negative, as the causative agent does not grow in ordinary culture media. We present the case of a 78-year-old man with a history of seronegative polyarthritis that was refractory to treatment with several biological agents for a duration of 5 years prior to presentation to the emergency department with stroke. Echocardiography revealed aortic valve endocarditis with a 3.6 cm vegetation and multiple smaller vegetations. The patient underwent surgery with aortic valve replacement followed by prolonged antibiotic treatment. 16 S rDNA PCR analysis of the resected valve revealed as the causative agent. Two years after surgery and treatment with antibiotics, the patient's previously longstanding arthritis had totally disappeared and all rheumatological treatment had been discontinued.
惠普尔病是一种罕见的多系统疾病,每年发病率小于百万分之一。该病常表现为多关节炎、腹泻和肠道吸收不良。少数患者会出现心内膜炎,且通常培养结果为阴性,因为病原体无法在普通培养基中生长。我们报告一例78岁男性患者,有血清阴性多关节炎病史,在使用多种生物制剂治疗5年无效后,因中风就诊于急诊科。超声心动图显示主动脉瓣心内膜炎,有一个3.6厘米的赘生物和多个较小的赘生物。患者接受了主动脉瓣置换手术,随后进行了长期抗生素治疗。对切除瓣膜进行的16S rDNA聚合酶链反应分析显示了病原体。手术和抗生素治疗两年后,患者先前长期存在的关节炎完全消失,所有风湿病治疗均已停止。