Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.
Haslam Family Endowed Chair in Cardiovascular Medicine, Department of Cardiovascular Medicine, Medical Director, Aorta Center, Heart and Vascular Institute, Cleveland Clinic, Cleveland, OH, USA.
Cleve Clin J Med. 2018 Jun;85(6):481-492. doi: 10.3949/ccjm.85a.17039.
Thoracic aortic aneurysm (TAA) is usually clinically silent and progresses slowly until a tipping point is reached, after which the aortic diameter can expand more rapidly and the condition can potentially end in aortic dissection or rupture. Causes include bicuspid aortic valve and genetic syndromes (Marfan, Loeys-Dietz, and Ehlers-Danlos syndromes) and familial associations, but many cases are idiopathic. Clinicians should therefore be alert for clues on chest imaging, and consider screening in first-degree relatives of patients known to have aortic disease. Early referral to a cardiologist specializing in aortic disease is key.
胸主动脉瘤(TAA)通常临床无症状,且进展缓慢,直到达到临界点,此后主动脉直径扩张速度加快,病情可能最终导致主动脉夹层或破裂。病因包括二叶式主动脉瓣和遗传综合征(马凡综合征、Loeys-Dietz 综合征和埃勒斯-当洛斯综合征)以及家族相关性,但许多病例为特发性。因此,临床医生应警惕胸部影像学检查中的线索,并考虑对已知患有主动脉疾病的患者的一级亲属进行筛查。早期转介至专门治疗主动脉疾病的心脏病专家是关键。