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胸主动脉瘤的病因、发病机制及治疗

Etiology, pathogenesis and management of thoracic aortic aneurysm.

作者信息

Ince Hüseyin, Nienaber Christoph A

机构信息

Division of Cardiology, University Hospital Rostock, Rostock School of Medicine, Rostock, Germany.

出版信息

Nat Clin Pract Cardiovasc Med. 2007 Aug;4(8):418-27. doi: 10.1038/ncpcardio0937.

Abstract

Given the growing proportion of elderly people in Western societies and the increasing prevalence of chronic hypertension, the management of aneurysmal aortic disease is an ever growing challenge. Although degenerative changes in the aortic wall are common to thoracic aortic aneurysm (TAA) and to various types of dissection in general, TAA can result from specific heritable disorders of connective tissues. Today, increased awareness of vascular diseases and access to tomographic imaging equipment facilitate the diagnosis of TAA, even when asymptomatic. While most TAA cases with ascending aortic involvement are treated with surgical repair (primarily valve-preserving techniques), aneurysms of the distal arch and descending thoracic aorta are amenable to alternatives to classic open repair such as the emerging endovascular treatment techniques. In this Review, we provide a comprehensive overview of the etiology, pathophysiology and clinical management of patients with TAA, and discuss the most recent literature on the condition.

摘要

鉴于西方社会老年人口比例不断增加以及慢性高血压患病率不断上升,动脉瘤性主动脉疾病的管理面临着日益严峻的挑战。尽管主动脉壁的退行性变是胸主动脉瘤(TAA)和一般各种类型夹层的共同特征,但TAA可能由结缔组织的特定遗传性疾病引起。如今,对血管疾病认识的提高以及断层成像设备的普及,即使在无症状的情况下也有助于TAA的诊断。虽然大多数累及升主动脉的TAA病例采用手术修复治疗(主要是保留瓣膜技术),但远端主动脉弓和降主动脉的动脉瘤适合采用经典开放修复的替代方法,如新兴的血管内治疗技术。在本综述中,我们全面概述了TAA患者的病因、病理生理学和临床管理,并讨论了有关该疾病的最新文献。

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