Okuyama Yurika, Kikuchi Koki, Stephenson Samuel David, Nishioka Naritomo, Doi Takahiro, Yamagishi Junya, Yuda Satoshi
Department of General Internal Medicine, Teine Keijinkai Hospital, Sapporo, Japan.
Department of Infectious Diseases, Teine Keijinkai Hospital, Sapporo, Japan.
BMC Infect Dis. 2025 May 8;25(1):682. doi: 10.1186/s12879-025-10913-7.
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.
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.
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.
嗜沫聚集杆菌(A. aphrophilus)是感染性心内膜炎(IE)的罕见病因,但却是公认的血培养阴性IE的病因。瓣膜病或人工瓣膜患者发生IE的风险增加。据我们所知,此前从未有过A. aphrophilus导致腰椎小关节关节炎合并IE的报道。
我们报告首例无既往心脏病史患者,血培养阴性的A. aphrophilus天然瓣膜IE以小关节关节炎为首发症状。一名58岁无已知心脏病史的日本男性,出现高热、寒战和下背部疼痛。初始实验室检查显示白细胞增多和转氨酶升高。经胸超声心动图显示主动脉瓣赘生物伴中度主动脉瓣反流。磁共振成像(MRI)显示右髂腰肌和L4/L5小关节有高强度区域,提示有液体聚集和播散性病变。多组血培养均未发现细菌生长。对血液和肝细胞(由于患者急性肝损伤)进行的16S核糖体RNA的广谱聚合酶链反应(br-PCR)也未能鉴定出病原体。患者出现心力衰竭,经食管超声心动图显示严重主动脉瓣反流以及主动脉瓣无冠瓣处有穿孔形成的动脉瘤。他接受了主动脉瓣置换术,症状迅速改善。尽管切除瓣膜的培养物为阴性,但对瓣膜组织进行的br-PCR最终证实存在嗜沫聚集杆菌。
这是首例报道的由嗜沫聚集杆菌引起的血培养阴性天然瓣膜IE,在无已知心脏病史的患者中表现为小关节关节炎。我们的病例强调了在发热和不明原因肌肉骨骼疼痛患者中考虑IE的重要性,即使没有已知心脏病史。当传统诊断测试无定论时,对切除的瓣膜组织进行br-PCR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。