Landin-Rey Elisa, Toubes-Navarro Maria Elena, Dominguez-Robla Miguel, Rey-Bascuas Maria, Valdes-Cuadrado Luis
Pneumology Department, Hospital Clínico Universitario de Santiago de Compostela, Spain.
Radiology Department, Hospital Clínico Universitario de Santiago de Compostela, Spain.
Multidiscip Respir Med. 2025 Jan 8;20(1):1004. doi: 10.5826/mrm.2025.1004.
Infective thoracic aortic aneurysms are uncommon, especially presenting with haemoptysis.
We report the case of an 81-year-old male who presented with fever and pleuritic chest pain and was initially misdiagnosed with community-acquired pneumonia. A CT scan later revealed a saccular, ruptured thoracic aortic aneurysm. Despite antibiotic therapy, the patient developed haemoptysis, necessitating thoracic endovascular aortic repair (TEVAR). Post-procedure, the patient showed significant clinical improvement and was discharged in stable condition 45 days later.
Infected thoracic aortic aneurysms presenting as haemoptysis are exceptionally rare but life-threatening. Early clinical suspicion (manifested by haemoptysis, fever and thoracic pain) is essential, particularly in patients with risk factors such as immunosuppression or previous infections. This case emphasizes the importance of prompt diagnosis and intervention, along with the use of appropriate imaging techniques to reduce morbidity and mortality associated with this rare yet severe condition.
感染性胸主动脉瘤并不常见,尤其是以咯血为表现的情况。
我们报告一例81岁男性患者,其表现为发热和胸膜炎性胸痛,最初被误诊为社区获得性肺炎。随后的CT扫描显示为囊状破裂胸主动脉瘤。尽管进行了抗生素治疗,患者仍出现咯血,需要进行胸主动脉腔内修复术(TEVAR)。术后,患者临床症状明显改善,45天后病情稳定出院。
以咯血为表现的感染性胸主动脉瘤极为罕见但危及生命。早期临床怀疑(表现为咯血、发热和胸痛)至关重要,尤其是对于有免疫抑制或既往感染等危险因素的患者。本病例强调了及时诊断和干预的重要性,以及使用适当的成像技术以降低与这种罕见但严重疾病相关的发病率和死亡率。