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[累及异常右锁骨下动脉的主动脉夹层动脉瘤]

[Dissecting aortic aneurysm involving an aberrant right subclavian artery].

作者信息

Fukushima K, Kamisawa O, Yamaguchi T, Misawa Y, Kato M, Hasegawa T

机构信息

Department of Thoracic and Cardiovascular Surgery, Jichi Medical School, Tochigi, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1992 Feb;40(2):278-81.

PMID:1593169
Abstract

A 51-year-old man was admitted with severe interscapular and chest pain. Chest X-ray showed marked widening of the mediastinum. Aortography demonstrated DeBakey IIIb type dissecting aortic aneurysm and an aberrant right subclavian artery arising from the diverticulum of Kommerell. The intimal tear was repaired with direct suture closure with the aid of femoro-femoral bypass. Although the dissecting lumen was not obliterated completely, the patient has been well for seven years on antihypertensive treatment. This is a rare combination of congenital and acquired disease of the aorta. As far as we know, this is the first report in Japanese literature.

摘要

一名51岁男性因严重的肩胛间区和胸痛入院。胸部X线显示纵隔明显增宽。主动脉造影显示为DeBakey IIIb型主动脉夹层动脉瘤,并有一条异常的右锁骨下动脉起源于Kommerell憩室。在内膜撕裂处借助股-股旁路进行直接缝合修复。尽管夹层腔未完全闭塞,但患者在接受抗高血压治疗后已健康存活7年。这是一种罕见的先天性和后天性主动脉疾病的组合。据我们所知,这是日本文献中的首例报告。

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