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用于洛伊斯-迪茨综合征的两阶段全主动脉置换术。

Two-stage total aortic replacement for Loeys-Dietz syndrome.

作者信息

Williams Matthew L, Wechsler Stephanie Burns, Hughes G Chad

机构信息

Division of Thoracic and Cardiovascular Surgery, Department of Surgery, Duke University, Durham, North Carolina 27710, USA.

出版信息

J Card Surg. 2010 Mar;25(2):223-4. doi: 10.1111/j.1540-8191.2009.00956.x.

Abstract

Loeys-Dietz syndrome (LDS) is a recently described connective tissue disorder characterized by generalized arterial tortuosity and aggressive aortopathy that untreated leads to early death even at aortic dimensions as small as 4 cm. We report the case of a young man with LDS successfully treated for aortic root, arch, and thoracoabdominal pathology.

摘要

洛伊迪茨综合征(LDS)是一种最近才被描述的结缔组织疾病,其特征为全身性动脉迂曲和侵袭性主动脉病变,未经治疗即使在主动脉直径小至4厘米时也会导致早期死亡。我们报告了一例患有LDS的年轻男性,其主动脉根部、主动脉弓及胸腹段病变均得到成功治疗。

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