用TEVAR修复MSSA胸椎真菌性动脉瘤1例。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Umabalan Thirupathy, Vikramaditya Samala Venkata, Viraj Panchal
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引用次数: 0

摘要

背景和临床意义:真菌性主动脉瘤是一种罕见但危及生命的血管疾病,其特征是感染引起的主动脉扩张或假性动脉瘤形成。这种情况具有破裂和死亡的高风险,特别是在患有潜在心血管疾病、近期接受过血管手术或患有免疫损害合并症(如糖尿病)的个体中。由于其非特异性症状,诊断具有挑战性,通常需要高度怀疑,特别是在出现持续发烧和初始影像学阴性的患者中。早期识别和干预至关重要,因为延迟治疗会显著恶化结果。病例介绍:一名68岁男性,有冠状动脉疾病史,近期植入支架,高血压,表现为发热、发冷、僵直和轻度非干咳2天。实验室结果仅对白细胞增多有显著意义。最初的胸部x光片和非对比CT扫描无明显变化。他被确诊为肺炎,并开始静脉注射抗生素。持续发热促使增强CT进一步检查,显示主动脉弓远端假性动脉瘤和轻度纵隔滞留。血液培养培养出甲氧西林敏感金黄色葡萄球菌(MSSA)。经胸超声心动图显示心内膜炎阴性。患者被转移到三级中心,重复成像证实一个1.5厘米的假性动脉瘤和一个4毫米的穿透性动脉粥样硬化性溃疡。在多学科评估后,他接受了胸腔血管内主动脉修复术(TEVAR),并完成了为期四周的头孢唑林静脉注射。随访影像显示动脉瘤修复成功,无并发症。结论:胸腔真菌性动脉瘤是一种快速致命的疾病,尽管介入治疗。鉴于其非特异性表现,临床高度怀疑是必要的。CTA是诊断该病最实用的方法。除抗生素外,TEVAR作为开放式手术修复(OSR)的一种可行且安全的替代方案正在获得关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MSSA Thoracic Mycotic Aneurysm Repaired with TEVAR: A Case Report.

Background and Clinical Significance: Mycotic aortic aneurysm is a rare but life-threatening vascular condition characterized by infection-induced dilation or pseudoaneurysm formation in the aorta. The condition carries a high risk of rupture and mortality, especially in individuals with underlying cardiovascular disease, who have undergone recent vascular procedures, or with immunocompromising comorbidities such as diabetes. Its diagnosis is challenging due to its non-specific symptoms and often requires a high index of suspicion, especially in patients presenting with persistent fever and negative initial imaging. Early recognition and intervention are critical, as delayed treatment significantly worsens outcomes. Case Presentation: A 68-year-old male with a history of coronary artery disease, recent stent placement, and hypertension presented with two days of fever, chills, rigors, and a mild nonproductive cough. The laboratory findings were only significant for leukocytosis. The initial chest X-ray and non-contrast CT scans were unremarkable. He was admitted for presumed pneumonia and started on intravenous antibiotics. Persistent fever prompted further investigation with contrast-enhanced CT, which revealed a distal-aortic-arch pseudoaneurysm and mild mediastinal stranding. Blood cultures grew methicillin-sensitive Staphylococcus aureus (MSSA). Transthoracic echocardiogram was negative for endocarditis. The patient was transferred to a tertiary center, where repeat imaging confirmed a 1.5 cm pseudoaneurysm and a 4 mm penetrating atherosclerotic ulcer. After multidisciplinary assessment, he underwent thoracic endovascular aortic repair (TEVAR) and completed four weeks of intravenous cefazolin. Follow-up imaging showed successful aneurysm repair with no complications. Conclusions: Thoracic mycotic aneurysm is a rapidly fatal entity despite intervention. High clinical suspicion is necessary given its non-specific presentation. It is diagnosed most practically using CTA. In addition to antibiotics, TEVAR is gaining traction as a feasible and a safe alternative to open surgical repair (OSR).

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