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无名动脉受累于IV型埃勒斯-当洛综合征。

Innominate artery involvement in type IV Ehlers-Danlos syndrome.

作者信息

Valverde A, Tricot J F, de Crepy B, Bakdach H, Djabbari K

机构信息

Service de Chirurgie Vasculaire et Thoracique, Hôpital André Mignot, Le Chesnay, France.

出版信息

Ann Vasc Surg. 1991 Jan;5(1):41-5. doi: 10.1007/BF02021776.

Abstract

We report two cases of innominate artery involvement in patients with Ehlers-Danlos syndrome. In the first patient, spontaneous dissection of the innominate artery was treated successfully. In the other, the patient died of spontaneous rupture of the innominate artery in the early postoperative course after operation for aneurysm of the celiac artery. Arterial complications occurring in Ehlers-Danlos syndrome are rare but pose difficult diagnostic and therapeutic problems for the vascular surgeon due to arterial wall fragility.

摘要

我们报告两例埃勒斯-当洛综合征患者出现无名动脉受累的病例。第一例患者,无名动脉自发性夹层分离经成功治疗。另一例患者,在接受腹腔动脉动脉瘤手术后的术后早期,因无名动脉自发性破裂死亡。埃勒斯-当洛综合征中出现的动脉并发症罕见,但由于动脉壁脆弱,给血管外科医生带来了诊断和治疗难题。

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