Calò Lorenzo, Botti Andrea, Carretta Tomas, De Rosa Fabrizio, Fiorini Roberto, Pedrazzini Massimo, Tortorella Giovanni
U.O. Cardiologia-UTIC, Ospedale Vaio, AUSL Parma, Fidenza (PR).
U.O. Radiodiagnostica, Ospedale Vaio, AUSL Parma, Fidenza (PR).
G Ital Cardiol (Rome). 2024 Aug;25(8):608. doi: 10.1714/4309.42930.
Pulmonary artery dissection is a rare and fatal disease. Diagnosis is mainly made during autopsy because most patients die suddenly due to pulmonary artery dissection in the pericardium resulting in pericardial tamponade. The optimum management is not clearly defined because of the paucity of cases in the literature. We describe the case of an 81-year-old man, affected by rheumatoid arthritis and with history of aortic valve replacement surgery, who attended an emergency department for non-specific symptoms, started complaining of chest pain rapidly deteriorated into cardiac shock. Computed tomography scan, performed on suspicion of an acute aortic pathology and/or a pulmonary embolism, allowed the identification of pulmonary artery dissection associated with aorto-pulmonary fistula. Despite early diagnosis in the emergency department, the outcome was unfortunately fatal.
肺动脉夹层是一种罕见的致命疾病。诊断主要在尸检时做出,因为大多数患者因心包内肺动脉夹层导致心包填塞而突然死亡。由于文献中病例稀少,最佳治疗方案尚未明确界定。我们描述了一名81岁男性的病例,他患有类风湿性关节炎且有主动脉瓣置换手术史,因非特异性症状前往急诊科就诊,随后开始抱怨胸痛,并迅速恶化为心源性休克。因怀疑急性主动脉病变和/或肺栓塞而进行的计算机断层扫描,发现了与主肺动脉瘘相关的肺动脉夹层。尽管在急诊科早期诊断,但不幸的是结果仍为致命。