弯曲杆菌胎儿假瓣膜心内膜炎表现为中风。

JMM case reports Pub Date : 2018-04-06 eCollection Date: 2018-05-01 DOI:10.1099/jmmcr.0.005147
Christina Petridou, Lenka Strakova, Ruan Simpson
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引用次数: 5

摘要

导读:弯曲杆菌是一种常见的胃肠道病原体,但侵袭性疾病罕见。弯曲杆菌胎儿可在骨髓炎、脑膜炎和关节感染中发挥作用,对血管内皮有预测作用,可引起真菌性动脉瘤、血栓性静脉炎和心内膜炎。在此,我们报告一例由C.胎儿引起的人工瓣膜心内膜炎,并复习文献。病例介绍:一名85岁妇女,因组织主动脉瓣置换术和心房颤动,因强直阵挛发作,右侧偏瘫,面部下垂和偏视入院。脑磁共振成像显示多发脑栓塞。血培养培养C.胎儿,超声心动图显示主动脉瓣增厚和运动受限,与2个月前再次在血培养中分离同一生物时所做的超声心动图有显著差异。经6周阿莫西林联合2周庆大霉素治疗人工瓣膜心内膜炎后病情好转。结论:既往仅有5例C.胎儿人工瓣膜心内膜炎报道,这是唯一一例表现为中风的患者。大多数存活的患者需要更换受影响的瓣膜,只有另外一名患者在没有手术的情况下存活。目前尚无关于c型胎儿心内膜炎最佳治疗的指南,本病例报告增加了对这种罕见且潜在毁灭性疾病的适当治疗的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Campylobacter fetus prosthetic valve endocarditis presenting as a stroke.

Introduction: Campylobacter is a common pathogen of the gastrointestinal tract, but invasive disease is rare. Campylobacter fetus can play a role in osteomyelitis, meningitis and joint infection and has a prediliction for the vascular endothelium, causing mycotic aneurysms, thrombophlebitis and endocarditis. Here we present a case of prosthetic valve endocarditis caused by C. fetus and a review of the literature.

Case presentation: An 85-year-old woman with a tissue aortic valve replacement and atrial fibrillation was admitted to hospital with tonic-clonic seizures, right-sided hemiparesis, facial droop and hemianopia. Multiple cerebral emboli were seen on magnetic resonance imaging of the brain. Blood cultures grew C. fetus and an echocardiogram showed thickening and restricted movement of the aortic valve, a significant difference from an echocardiogram done 2 months before when the same organism was again isolated in blood cultures. She improved after treatment with 6 weeks of amoxicillin and 2 weeks of synergistic gentamicin for prosthetic valve endocarditis.

Conclusion: There have only been five previously reported cases of C. fetus prosthetic valve endocarditis and this is the only patient who presented as a stroke. The majority of surviving patients required replacement of the affected valve with only one other patient surviving in the absence of surgery. No guidelines exist on the optimum treatment of C. fetus endocarditis and this case reports adds to the growing literature on the appropriate management for this rare and potentially devastating disease.

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