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感染性心内膜炎继发霉菌性胸主动脉瘤合并主动脉食管瘘的快速形成。

Rapid formation of aortoesophageal fistula complicated by mycotic thoracic aortic aneurysm secondary to infective endocarditis.

作者信息

Setake Maki, Uechi Yasuhiro, Kinjo Yuzuru, Miyazato Masaru, Nakachi Noriya, Tomiyama Ryosaku, Higa Namio, Hokama Akira

机构信息

Gastroenterology, Naha City Hospital, Japan.

Gastroenterology, Naha City Hospital.

出版信息

Rev Esp Enferm Dig. 2025 Apr;117(4):223-224. doi: 10.17235/reed.2024.10397/2024.

Abstract

A 73-year-old man was admitted with four weeks of intermittent fever. He had a history of total aortic arch replacement for aortic arch aneurysm four years prior. CT scans showed no abnormalities before admission. Repeated blood cultures yielded Streptococcus anginosus and Prevotella melaninogenica, suggesting infective endocarditis (IE). Transesophageal echocardiography revealed a vegetation on the aortic valve, confirming IE. He suddenly presented with massive hematemesis and hypotension. Endoscopy revealed an elevated lesion with a laceration but no active bleeding in the esophagus. CT scans showed a thoracic aneurysm involving the esophagus. A diagnosis of aortoesophageal fistula (AEF) complicated by mycotic thoracic aortic aneurysm (MTAA) was made, and he underwent stent graft interpolation followed by minimally invasive esophagectomy. MTAAs are more prone to rupture than arteriosclerotic aneurysms as they are usually not true but pseudoaneurysms. Antecedent infection, including endocarditis, sepsis, predisposes to MTAA. AEF is a rare but life-threatening cause of gastrointestinal bleeding characterized by Chiari's triad. There have been no reports of such rapid formation of AEF after the graft replacement, as shown here. A recent article reported a rapid formation (16 days) of AEF after thoracic endovascular aortic repair, emphasizing prosthetic infection as the most important risk factor. Our case underscores the importance of suspecting AEF and conducting repeated appropriate examinations even if initial examinations do not reveal any aneurysms.

摘要

一名73岁男性因持续四周的间歇性发热入院。他四年前曾因主动脉弓动脉瘤接受全主动脉弓置换术。入院前CT扫描未显示异常。多次血培养结果显示为咽峡炎链球菌和产黑色素普雷沃菌,提示感染性心内膜炎(IE)。经食管超声心动图显示主动脉瓣上有赘生物,确诊为IE。他突然出现大量呕血和低血压。内镜检查发现食管有一个隆起性病变伴一处撕裂伤,但无活动性出血。CT扫描显示一个累及食管的胸段动脉瘤。诊断为主动脉食管瘘(AEF)合并霉菌性胸主动脉瘤(MTAA),他接受了支架植入术,随后进行了微创食管切除术。MTAA比动脉硬化性动脉瘤更容易破裂,因为它们通常不是真性动脉瘤而是假性动脉瘤。包括心内膜炎、败血症在内的先前感染易引发MTAA。AEF是一种罕见但危及生命的胃肠道出血原因,其特征为Chiari三联征。如此处所示,移植置换术后如此迅速形成AEF尚无报道。最近一篇文章报道了胸段血管腔内主动脉修复术后AEF的快速形成(16天),强调人工瓣膜感染是最重要的危险因素。我们的病例强调了即使初始检查未发现任何动脉瘤,也需怀疑AEF并进行反复适当检查的重要性。

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