Facet joint arthritis as the presenting symptom for culture-negative Aggregatibacter aphrophilus native valve endocarditis in a patient without known cardiac disease: a case report.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Yurika Okuyama, Koki Kikuchi, Samuel David Stephenson, Naritomo Nishioka, Takahiro Doi, Junya Yamagishi, Satoshi Yuda
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Abstract

Background: Aggregatibacter aphrophilus (A. aphrophilus) is a rare cause of infective endocarditis (IE), but is a recognized cause of culture-negative IE. The risk of developing IE is increased in patients with valvular disease or prosthetic valves. To our knowledge, A. aphrophilus has never previously been reported to cause lumbar facet joint arthritis in combination with IE.

Case presentation: We present the first case where facet joint arthritis was the presenting symptom for culture-negative A. aphrophilus native valve IE in a patient with no prior cardiac disease. A 58-year-old Japanese male without known cardiac disease, presented with high fever, chills, and lower back pain. Initial laboratory evaluation showed leukocytosis and transaminitis. Transthoracic echocardiography revealed an aortic valve vegetation with moderate aortic regurgitation. Magnetic resonance imaging (MRI) showed high-intensity areas in the right iliopsoas muscle and L4/L5 facet joint, indicative of fluid accumulation and disseminated lesions. Multiple sets of blood cultures showed no bacterial growth. Broad-range polymerase chain reaction (br-PCR) for 16S ribosomal RNA on both blood and hepatocytes (due to the patient's acute liver damage) also failed to identify the causative organism. The patient developed heart failure, and transesophageal echocardiography showed severe aortic regurgitation and an aneurysm at the noncoronary cusp of the aortic valve with perforation. He underwent aortic valve replacement and his symptoms were promptly improved. Although cultures from the excised valve were negative, br-PCR on the valve tissue eventually confirmed the presence of A. aphrophilus.

Conclusion: This is the first reported case of culture-negative native valve IE caused by A. aphrophilus presenting with facet joint arthritis in a patient without known cardiac disease. Our case emphasizes the importance of considering IE in patients with fever and unexplained musculoskeletal pain, even without known cardiac disease. When conventional diagnostic tests are inconclusive, br-PCR on excised valve tissue is indispensable. Further improvements in non-invasive diagnostic methods are needed to facilitate early diagnosis and treatment.

以小关节关节炎为主要症状的培养阴性嗜aphophilus聚集杆菌原生瓣膜心内膜炎患者无已知心脏疾病:1例报告。
背景:嗜aphrophilus聚集杆菌(a.a aphrophilus)是一种罕见的感染性心内膜炎(IE)的病因,但却是公认的培养阴性IE的病因。患有瓣膜疾病或人工瓣膜的患者发生IE的风险增加。据我们所知,以前从未报道过嗜蚜杆菌引起腰椎小关节关节炎合并IE。病例介绍:我们报告了第一例以小关节关节炎为主要症状的培养阴性假单胞杆菌原生瓣膜IE患者,既往无心脏病。58岁日本男性,无已知心脏病,表现为高热、寒战和下背部疼痛。初步实验室检查显示白细胞增多和转氨炎。经胸超声心动图显示主动脉瓣植被和中度主动脉反流。磁共振成像(MRI)显示右侧髂腰肌和L4/L5小关节高强度区,提示积液和弥散性病变。多组血液培养均未发现细菌生长。血液和肝细胞(由于患者的急性肝损伤)上16S核糖体RNA的广谱聚合酶链反应(br-PCR)也未能识别致病生物。患者出现心力衰竭,经食管超声心动图显示严重的主动脉反流和主动脉瓣非冠状动脉尖端的动脉瘤穿孔。他接受了主动脉瓣置换术,症状迅速改善。虽然切除瓣膜的培养结果为阴性,但对瓣膜组织的br-PCR最终证实了阿佛洛菲菌的存在。结论:这是首次报道的由嗜蚜螨引起的培养阴性的先天性瓣膜IE,在没有已知心脏病的患者中表现为小关节关节炎。我们的病例强调了在有发热和不明原因的肌肉骨骼疼痛的患者中考虑IE的重要性,即使没有已知的心脏疾病。当传统的诊断测试是不确定的,br-PCR对切除的瓣膜组织是必不可少的。需要进一步改进非侵入性诊断方法,以促进早期诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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