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一名男性自发性左冠状动脉主干夹层

Spontaneous Left Main Coronary Artery Dissection in a Male.

作者信息

Chopra Lakshay, Maenza Joseph, Chang Chih-Chiun, Rashid Syed Muhammad Ibrahim, Kanei Yumiko

机构信息

Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.

Cardiology, Icahn School of Medicine at Mount Sinai, New York, USA.

出版信息

Cureus. 2024 May 19;16(5):e60587. doi: 10.7759/cureus.60587. eCollection 2024 May.

Abstract

Spontaneous coronary artery dissection (SCAD) is one of the causes of acute coronary syndrome (ACS) that is increasingly recognized in young to middle-aged women without typical coronary risk factors. This case report describes a 46-year-old male with a rare presentation of SCAD involving the left main (LM) coronary artery. The patient underwent an emergency coronary angiogram for high-risk ACS and had percutaneous coronary intervention (PCI) of LM due to active ischemia and hemodynamic instability. The extension of intramural hematoma after the LM coronary artery stent confirmed the initial suspicion of SCAD. The diagnosis of SCAD is crucial, as its management differs from other causes of ACS. Coronary angiography is the gold standard for diagnosing SCAD, with adjunctive imaging using optical coherence tomography (OCT) and intravascular ultrasound (IVUS). In this patient, his physical examination findings and further imaging raised a suspicion for systemic connective tissue disease. Genetic analysis was executed, but no reportable variants in any of the 29 genes studied were identified. This case highlights the importance of recognizing SCAD as a potential cause of ACS even in men and emphasizes the findings during coronary angiography that can aid in an accurate diagnosis and appropriate management.

摘要

自发性冠状动脉夹层(SCAD)是急性冠状动脉综合征(ACS)的病因之一,在无典型冠状动脉危险因素的中青年女性中越来越受到认可。本病例报告描述了一名46岁男性,其SCAD表现罕见,累及左主干(LM)冠状动脉。该患者因高危ACS接受了急诊冠状动脉造影,并因活动性缺血和血流动力学不稳定对LM进行了经皮冠状动脉介入治疗(PCI)。LM冠状动脉支架置入术后壁内血肿的扩展证实了最初对SCAD的怀疑。SCAD的诊断至关重要,因为其治疗方法与ACS的其他病因不同。冠状动脉造影是诊断SCAD的金标准,辅助成像可使用光学相干断层扫描(OCT)和血管内超声(IVUS)。在该患者中,其体格检查结果和进一步的影像学检查引发了对系统性结缔组织病的怀疑。进行了基因分析,但在所研究的29个基因中均未发现可报告的变异。本病例强调了即使在男性中也应认识到SCAD是ACS潜在病因的重要性,并强调了冠状动脉造影检查中有助于准确诊断和适当治疗的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/427f/11184538/8d6a873000df/cureus-0016-00000060587-i01.jpg

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