Stanford Type A Aortic Dissection Masquerading as Acute Ischemic Stroke: A Case Report.

IF 2.9 Q1 EMERGENCY MEDICINE
Archives of Academic Emergency Medicine Pub Date : 2024-11-21 eCollection Date: 2025-01-01 DOI:10.22037/aaem.v13i1.2409
Chao Liu, Jiangrong Ma, Bo Zhang, Ji Xie, Liyu Lu, Shinan Nie
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引用次数: 0

Abstract

Aortic dissection (AD), a life-threatening cardiovascular emergency, is characterized by the separation of the aorta's inner and middle layers due to a tear in the intima. It is classified as Stanford type A or B based on the tear's location and extent. Symptoms vary but commonly include severe pain in the chest, back, or abdomen, along with atypical presentations such as shock, heart failure, or syncope. End-organ ischemia, including stroke and limb necrosis, may occur. Timely diagnosis and intervention are crucial for survival. Here, we report a 31-year-old male patient who presented with acute neurological symptoms, initially suspected of having a stroke, but was ultimately diagnosed with Stanford type A AD upon computed tomography (CT) angiography. This case underscores the importance of considering AD in the differential diagnosis of patients with neurological symptoms for accurate and prompt management.

斯坦福A型主动脉夹层伪装成急性缺血性中风1例报告。
主动脉夹层(Aortic dissection, AD)是一种危及生命的心血管急症,其特征是由于内膜撕裂导致主动脉内层和中间层分离。根据撕裂的位置和程度将其分为斯坦福A型或B型。症状各不相同,但通常包括胸部、背部或腹部的剧烈疼痛,并伴有非典型症状,如休克、心力衰竭或晕厥。终末器官缺血,包括中风和肢体坏死,可能发生。及时诊断和干预对生存至关重要。在这里,我们报告了一位31岁的男性患者,他表现出急性神经系统症状,最初怀疑有中风,但最终通过计算机断层扫描(CT)血管造影诊断为斯坦福a型AD。本病例强调了在神经系统症状患者鉴别诊断中考虑AD的重要性,以获得准确和及时的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of Academic Emergency Medicine
Archives of Academic Emergency Medicine Medicine-Emergency Medicine
CiteScore
8.90
自引率
7.40%
发文量
0
审稿时长
6 weeks
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