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一名儿童因埃勒斯-当洛综合征引发的肱动脉瘤。

A brachial aneurysm in childhood caused by Ehlers-Danlos syndrome.

作者信息

Sayin A G, Bozkurt A K, Cangel U, Köksal C, Oz B

机构信息

Department of Thoracic and Cardiothoracic Surgery, University of Istanbul, Cerrahpaşa Medical Faculty, Istanbul, Turkey.

出版信息

J Cardiovasc Surg (Torino). 2001 Oct;42(5):687-9.

Abstract

A case of an 11-year-old boy with Ehlers-Danlos syndrome (EDS) type IV is presented. He was referred with a pulsatile mass above the right antecubital fossa and Doppler revealed a saccular aneurysm. Excision and ligation of the brachial artery aneurysm was performed. The diagnosis was confirmed by skin fibroblast cultures and histopathologic evaluation. We conclude that arteriography should be avoided in EDS and color-Doppler should be the sole means of diagnosis. Ligation rather than arterial reconstruction should be preferred.

摘要

本文报告一例11岁患有IV型埃勒斯-当洛综合征(EDS)的男孩。他因右肘前窝上方有搏动性肿块前来就诊,多普勒检查显示为囊状动脉瘤。遂对肱动脉动脉瘤进行了切除和结扎。通过皮肤成纤维细胞培养和组织病理学评估确诊。我们得出结论,EDS患者应避免进行动脉造影,彩色多普勒应作为唯一的诊断手段。应首选结扎而非动脉重建。

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