Kordzadeh Ali, Rhodes Karen May, Hanif Muhammad Asad, Scott Harriet, Panayiotopoulos Yiannis
Department of Vascular Surgery, Mid Essex Hospitals Services NHS Trust, Broomfield Hospital, Essex, UK.
Ann Vasc Surg. 2013 Oct;27(7):973.e9-17. doi: 10.1016/j.avsg.2012.08.016. Epub 2013 May 22.
The aim of this study is to describe a case of ruptured cryptogenic mycotic abdominal aortic aneurysm by Salmonella enteritidis (SE) and present a comprehensive review of the literature.
A 66-year-old man with a past medical history of coronary artery bypass graft (CABG) and polymylagia rheumatica (PMR) presented with a 2-day history of right-flank-to-groin pain and fever. He was found to have tenderness on the right of the umbilical region and laboratory data showed leukocytosis, raised C-reactive protein, and a significant drop in hemoglobin level as compared with his first visit 17 days earlier, with no hemodynamic instability. An immediate computed tomography angiogram (CTA) was performed, which showed a 4-cm, fusiform, ruptured infrarenal aortic aneurysm. Exploratory laparatomy was performed and the aorta was isolated and excised from the infrarenal level to the common iliac bificuration. A straight silver Dacron graft soaked in rifampicin was placed with an end-to-end anastomosis. The excised aorta and the lymph nodes were sent for histologic and microbiologic assessment.
Blood culture and specimen microbiology grew Salmonella enteritidis (SE). The histology exhibited atherosclerosis at the rupture point with decreasing neutrophil deposition from the intima to the adventitia layer, respectively.
Infrarenal abdominal mycotic aneurysm (MA) by SE was observed and showed vague, nonspecific signs and symptoms. We recommend a high index of suspicion and low threshold for use of CT imaging in any infected patient of age >60 years with fever and abdominal pain on a background of diabetes and connective tissue disease. A comprehensive review of the literature was performed due to a lack of consensus on the best surgical treatment and limited information on the path of SE-induced aortitis or MA from presentation to final outcome.
本研究旨在描述一例由肠炎沙门氏菌(SE)引起的隐源性霉菌性腹主动脉瘤破裂病例,并对相关文献进行全面综述。
一名66岁男性,有冠状动脉旁路移植术(CABG)和风湿性多肌痛(PMR)病史,出现右侧腹至腹股沟疼痛及发热2天。发现其脐区右侧有压痛,实验室检查显示白细胞增多、C反应蛋白升高,与17天前首次就诊时相比血红蛋白水平显著下降,无血流动力学不稳定。立即进行了计算机断层扫描血管造影(CTA),显示一个4厘米的梭形肾下腹主动脉瘤破裂。进行了剖腹探查术,将主动脉从肾下水平至髂总分叉处分离并切除。放置了一段浸泡在利福平中的直银聚酯人工血管,进行端端吻合。切除的主动脉和淋巴结送去进行组织学和微生物学评估。
血培养和标本微生物学检查培养出肠炎沙门氏菌(SE)。组织学显示破裂点处有动脉粥样硬化,中性粒细胞沉积从内膜到外膜层逐渐减少。
观察到由SE引起的肾下腹霉菌性动脉瘤(MA),其症状和体征模糊且不具特异性。我们建议,对于任何年龄>60岁、有糖尿病和结缔组织病背景、发热且腹痛的感染患者,应高度怀疑并降低使用CT成像的阈值。由于对于最佳手术治疗缺乏共识,且关于SE引起的主动脉炎或MA从发病到最终结局的病程信息有限,因此进行了全面的文献综述。