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经胸超声心动图诊断在完全无症状的患者中升主动脉内悬挂团块。

A hanging mass in the ascending aorta diagnosed by transthoracic echocardiography in a totally asymptomatic subject.

机构信息

Cardiology Division, Spedali Riuniti, Livorno, Italy.

出版信息

J Am Soc Echocardiogr. 2009 Oct;22(10):1197.e5-7. doi: 10.1016/j.echo.2009.04.017.

DOI:10.1016/j.echo.2009.04.017
PMID:19801313
Abstract

Aortic mural thrombosis is generally associated with several diseases, including coagulopathies, aortic dissection or trauma, tumors, and complicated atherosclerotic plaques. The development of a friable mobile thrombus, especially in the ascending aorta or proximal aortic arch, is a rare event with potentially ominous consequences because of a life-threatening risk of stroke and peripheral embolization. The treatment of choice of this condition is still controversial. We report a case of an absolutely asymptomatic 57-year-old patient with a mobile, pedunculated mass attached to the posterior wall of an otherwise normal ascending aorta. The aortic mass, identified by transthoracic echocardiography, was surgically removed and demonstrated to be a thrombus, and the aortic wall specimen was microscopically normal.

摘要

主动脉壁血栓形成通常与多种疾病相关,包括凝血障碍、主动脉夹层或创伤、肿瘤以及复杂的粥样硬化斑块。易碎的活动性血栓的形成,特别是在升主动脉或主动脉弓近端,是一种罕见的事件,具有潜在的严重后果,因为有发生中风和外周栓塞的致命风险。这种情况的治疗选择仍然存在争议。我们报告了一例 57 岁的绝对无症状患者,其升主动脉的后壁附着有一个活动性的、带蒂的肿块。经胸超声心动图发现的主动脉肿块被手术切除,证实为血栓,主动脉壁标本显微镜下正常。

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A hanging mass in the ascending aorta diagnosed by transthoracic echocardiography in a totally asymptomatic subject.经胸超声心动图诊断在完全无症状的患者中升主动脉内悬挂团块。
J Am Soc Echocardiogr. 2009 Oct;22(10):1197.e5-7. doi: 10.1016/j.echo.2009.04.017.
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Use of three dimensional-printing in the management of floating aortic thrombus due to occult aortic dissection: A case report.三维打印技术在隐匿性主动脉夹层所致漂浮性主动脉血栓管理中的应用:一例报告
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Aortic Mural Thrombus in Association with Occult Aortic Dissection.
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CASE (Phila). 2017 Apr 24;1(2):62-64. doi: 10.1016/j.case.2017.01.001. eCollection 2017 Apr.
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Non-atherosclerotic aortic mural thrombus: a rare source of embolism.非动脉粥样硬化性主动脉壁血栓:一种罕见的栓子来源。
BMJ Case Rep. 2017 Aug 1;2017:bcr-2017-220592. doi: 10.1136/bcr-2017-220592.