一种罕见的急性胸主动脉夹层表现。

MacKenzie Barton, Hao Wang
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引用次数: 1

摘要

我们报告一例40岁的白人男性,既往有多种药物滥用史(可卡因和甲基苯丙胺),他到急诊科(ED)主诉间歇性咳嗽并伴有胸部不适和呼吸急促2周。最初的生命体征表现为边缘性心动过速(每分钟98次)、呼吸急促(每分钟37次)和缺氧(室内空气氧饱和度89%),体检结果一般。初步检查包括计算机断层血管造影(CTA)显示A型主动脉夹层,累及胸部和腹部,患者入院。该患者行了升主动脉切除术合并移植物置放、体外循环、复合假体主动脉根置换术和左右冠状动脉重建和再植,并度过了复杂的住院过程。这个病例证明了娱乐性药物使用,特别是兴奋剂如可卡因和安非他明与急性主动脉夹层(AAD)之间存在的典型联系。然而,在多物质使用的情况下,这种边缘性亚急性无痛性夹层的表现提出了进一步的问题,因为罕见的AAD通常在高危人群中发现,如结缔组织疾病(Marfan综合征、ehers - danlos综合征、loeyss - dietz综合征)、二尖瓣主动脉瓣、慢性高血压或既往主动脉病变。因此,我们建议临床医生强烈考虑将不常见的AAD作为其已知或高度怀疑的多药物滥用患者鉴别诊断的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Uncommon Presentation of Acute Thoracic Aortic Dissection.

An Uncommon Presentation of Acute Thoracic Aortic Dissection.

An Uncommon Presentation of Acute Thoracic Aortic Dissection.

An Uncommon Presentation of Acute Thoracic Aortic Dissection.

We present a case of a 40-year-old Caucasian male with past medical history of polysubstance abuse (cocaine and methamphetamine), who presented to the emergency department (ED) complaining of intermittent cough with associated chest discomfort and shortness of breath for 2 weeks. Initial vital signs demonstrated borderline tachycardia (98 beats per minute), tachypnea (37 times per minutes), and hypoxia (oxygen saturation 89% on room air), and his physical exam was grossly unremarkable. A preliminary workup including a computed tomography angiography (CTA) revealed a type A aortic dissection with both thoracic and abdominal involvement for which the patient was admitted. This patient had resection of the ascending aorta with graft placement, cardiopulmonary bypass, aortic root replacement using composite prosthesis and left and right coronary reconstruction and reimplantation and survived a complicated hospital course. This case demonstrates the classic association known to exist between recreational drug use, specifically stimulants such as cocaine and amphetamines, and acute aortic dissection (AAD). However, such a presentation of borderline subacute, painless dissection in the setting of polysubstance use raises further questions, since uncommon AAD is typically found in higher-risk populations such as those with connective tissue disorders (Marfan syndrome, Ehlers-Danlos syndrome, Loeys-Dietz syndrome), bicuspid aortic valve, chronic hypertension, or previous aortic pathology. We therefore suggest clinicians strongly consider uncommon AAD as part of their differential diagnosis in patients with known or highly suspected polysubstance abuse.

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