Clinical Presentation and Management of Primary Mycotic Aortic Aneurysms: A Single Center Experience and Review of the Literature

Badreldin Mohamed, S. Taha, L. Navaro, M. Cusso, T. Barakat, S. Babikir, D. Taran, C. Marson, T. Ojimba, D. Mirghani, S. Naqvi, R. Eifell
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Abstract

Background: Primary mycotic aortic aneurysm (PMAA) is a localized dilation of the aortic wall caused by direct spread of bacteria via the bloodstream to the aortic wall and subsequent development of an aneurysm. The term mycotic aortic aneurysm was first used to describe a patient with four aortic aneurysms which have a mushroom-like appearance, and the term has since been used. Aim: To conduct a literature review and to report a series of cases of infra-renal mycotic aortic aneurysms, their presentation and subsequent outcome and management. Methods: Information was gathered retrospectively from medical records for patients who were over the age of 18 and who had presented with PMAAs at Cumberland infirmary o from April 2016 to July 2022. Results: A total of six patients were assessed in our study, mean age was 57-88 years. Presenting complains were: Back pain (n=2), abdominal pain (n=1), fever (n=4), collapsed (n=2), confusion (n=1) and other clinical presentations were leg pain, feeling unwell and malaise each reported in one patient each. Potential risk factors for PMAA identified were malignancy (n=2), diabetes mellitus (n=2), chronic kidney disease (n=2), immunosuppressive medication (n=2) and alcohol misuse (n=1). Potential sources of infection were retroperitoneal inflammation (n=1), pyelonephritis (n=1), retroperitoneal /psoas infection (n=2), duodenitis (n=1), systemic sepsis (n=1). Management can be surgical intervention such as Endovascular aortic repair (EVAR) (n=2), or axillo-bifemoral bypass (n=2) all of them had post-operative antibiotics or only antibiotics (n=3), however two patients of them died. Conclusion: PMAAs are rare but they have high risk of morbidity and mortality. The diagnosis is challenging but CT A-abdomen and pelvis remains valuable for diagnosis. Surgery, either bypass or EVAR with antibiotics, is a cornerstone for management, however other alternatives can be considered.
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原发性真菌性主动脉瘤的临床表现和治疗:单中心经验和文献回顾
背景:原发性真菌性主动脉瘤(PMAA)是一种由细菌通过血流直接传播到主动脉壁并随后发展成动脉瘤引起的局部主动脉壁扩张。霉菌性主动脉瘤一词最初用于描述有四个呈蘑菇样外观的主动脉瘤的患者,并且该术语已被使用。目的:对肾下真菌性主动脉瘤的临床表现、预后及治疗进行文献回顾和报道。方法:回顾性收集2016年4月至2022年7月在Cumberland医院就诊的18岁以上PMAAs患者的病历资料。结果:本研究共纳入6例患者,平均年龄57 ~ 88岁。主诉为:背部疼痛(n=2)、腹痛(n=1)、发热(n=4)、虚脱(n=2)、精神错乱(n=1),其他临床表现为腿部疼痛、感觉不适和不适,各有1例。PMAA的潜在危险因素为恶性肿瘤(n=2)、糖尿病(n=2)、慢性肾病(n=2)、免疫抑制药物(n=2)和酒精滥用(n=1)。潜在感染源为腹膜后炎症(n=1)、肾盂肾炎(n=1)、腹膜后/腰肌感染(n=2)、十二指肠炎(n=1)、全身性败血症(n=1)。治疗可采取手术干预,如血管内主动脉修复术(EVAR) (n=2)或腋双侧搭桥术(n=2),所有患者术后均使用抗生素或仅使用抗生素(n=3),但其中2例死亡。结论:PMAAs虽少见,但有较高的发病率和死亡率。诊断是具有挑战性的,但CT a -腹部和骨盆仍然是有价值的诊断。手术,无论是搭桥手术还是使用抗生素的EVAR,都是治疗的基础,但也可以考虑其他选择。
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