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复发性多软骨炎所致复杂性胸主动脉瘤的修复

Repair of a complex thoracic aneurysm from relapsing polychondritis.

作者信息

Jacobs Chad E, March Robert J, Hunt Peter J, Rivera Aksim G, Cavanagh Sherry, McCarthy Walter J

机构信息

Division of Vascular Surgery, Rush University Medical Center, Chicago, IL 60612, USA.

出版信息

Vasc Endovascular Surg. 2013 Jul;47(5):387-9. doi: 10.1177/1538574413488459. Epub 2013 May 8.

Abstract

A 29-year-old female with a history of relapsing polychondritis (RP) and open repair of a proximal descending thoracic aneurysm presented with 2 areas of asymptomatic thoracic aortic aneurysmal dilatation. The patient returned 3 months later with symptomatic aneurysm expansion, and she underwent ascending aortic arch replacement. She subsequently underwent staged endovascular repair of the distal descending thoracic aorta. RP is a rare disorder with an incidence of 3.5 per million persons annually, 4% to 7% of whom develop aneurysmal disease. Because of the aneurysmal potential of this disease, it is important for vascular surgeons to be aware of its presentation and treatment. To our knowledge, this is the first reported case describing endovascular technique to treat such a patient.

摘要

一名29岁女性,有复发性多软骨炎(RP)病史且曾接受近端降主动脉瘤开放修复术,此次出现2处无症状性胸主动脉瘤样扩张。患者3个月后因有症状的动脉瘤扩张复诊,接受了升主动脉弓置换术。随后她分期接受了降主动脉远端的血管腔内修复术。RP是一种罕见疾病,年发病率为百万分之3.5,其中4%至7%会发展为动脉瘤疾病。鉴于该疾病有形成动脉瘤的可能性,血管外科医生了解其表现和治疗方法很重要。据我们所知,这是首例报道描述采用血管腔内技术治疗此类患者的病例。

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