Service of Internal Medicine, Department of Medicine, Geneva University Hospitals, Geneva, Switzerland.
Department of Pathology and Immunology, University of Geneva, Faculty of Medicine, Geneva, Switzerland.
BMC Infect Dis. 2019 Apr 16;19(1):326. doi: 10.1186/s12879-019-3953-z.
Endograft infection is a rare but extremely dangerous complication of aortic repair (25-100% of mortality). We describe here the first case of Listeria monocytogenes abdominal periaortitis associated with a vascular graft. We also discuss the differential diagnosis of periaortitis and provide a literature review of L. monocytogenes infectious aortitis.
Nine months after endovascular treatment of an abdominal aortic aneurysm (abdominal stent graft), a 76-year-old man was admitted for severe abdominal pain radiating to the back. Laboratory tests were normal apart from elevated C-reactive protein (CRP). Injected abdominal computed tomography (CT) showed infiltration of the fat tissues around the aortic endoprosthesis and aneurysmal sac expansion; positron emission tomography with 2-deoxy-2-[fluorine-18]fluoro- D-glucose integrated with computed tomography (18F-FDG PET/CT) showed a hypermetabolic mass in contact with the endoprosthesis. Blood cultures were negative. At surgical revision, an infra-renal peri-aortic abscess was evident; post-operative antibiotic therapy with ciprofloxacin and doxycycline was started. Cultures of intraoperative samples were positive for L. monocytogenes. Results were further confirmed by a broad-range polymerase chain reaction (PCR) and next-generation sequencing. Antibiotic treatment was switched to intravenous amoxicillin for 6 weeks. Evolution was uneventful with decrease of inflammatory parameters and regression of the abscess.
An etiologic bacterial diagnosis before starting antibiotic therapy is paramount; nevertheless, culture-independent methods may provide a microbiological diagnosis in those cases where antimicrobials are empirically used and when cultures remain negative.
主动脉修复术后(25-100%的死亡率)发生移植物感染是一种罕见但极其危险的并发症。我们在此描述首例李斯特菌单核细胞增生症腹主动脉旁炎伴血管移植物感染。我们还讨论了腹主动脉旁炎的鉴别诊断,并对李斯特菌感染性动脉炎的文献进行了回顾。
一名 76 岁男性在腹主动脉瘤(腹主动脉支架移植物)血管内治疗 9 个月后,因严重腹痛放射至背部而入院。实验室检查除 C 反应蛋白(CRP)升高外均正常。腹部 CT 平扫和增强扫描显示主动脉内支架周围脂肪组织浸润和动脉瘤囊扩张;正电子发射断层扫描与 2-脱氧-2-[氟-18]氟-D-葡萄糖结合计算机断层扫描(18F-FDG PET/CT)显示与移植物接触的高代谢肿块。血培养阴性。在手术翻修时,发现肾下主动脉旁脓肿;术后开始使用环丙沙星和强力霉素进行抗生素治疗。术中样本的培养结果为李斯特菌阳性。广谱聚合酶链反应(PCR)和下一代测序进一步证实了结果。将抗生素治疗方案改为静脉注射阿莫西林 6 周。炎症参数下降,脓肿消退,病情平稳。
在开始抗生素治疗前进行细菌病因学诊断至关重要;然而,在经验性使用抗生素且培养结果仍为阴性的情况下,非培养方法可能提供微生物学诊断。