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成人期首次诊断为冠状动脉左主干起源异常综合征:心脏骤停的罕见原因

[First diagnosis of ALCAPA syndrome in adulthood: a rare cause of cardiac arrest].

作者信息

Urban Tim, Grundmann Sebastian, Klein Franziska, Wengenmayer Tobias, Müller-Peltzer Katharina, Busch Hans-Jörg

机构信息

Zentrum für Notfall- und Rettungsmedizin, Universitätsklinikum Freiburg, Sir-Hans-A.-Krebs-Straße, 79106, Freiburg, Deutschland.

Klinik für Kardiologie und Angiologie, Universitäts-Herzzentrum Freiburg - Bad Krozingen, Freiburg, Deutschland.

出版信息

Inn Med (Heidelb). 2025 Jan;66(1):124-128. doi: 10.1007/s00108-024-01782-4. Epub 2024 Sep 20.

Abstract

A 42-year-old patient with return of spontaneous circulation (ROSC) following an out-of-hospital cardiac arrest was referred to the authors' emergency department. The initial rhythm was ventricular fibrillation. A computed tomography scan and subsequent coronary angiography revealed anomalous left coronary artery from the pulmonary artery (ALCAPA) syndrome as the cause of this condition. A thickened right coronary artery with significant collateral blood flow to the left coronary artery was observed. After initial treatment in the authors' intensive care unit, surgical intervention was performed. The patient was discharged from hospital without any neurological damage.

摘要

一名42岁院外心脏骤停后恢复自主循环(ROSC)的患者被转诊至作者所在的急诊科。初始心律为室颤。计算机断层扫描及随后的冠状动脉造影显示,肺动脉起源的异常左冠状动脉(ALCAPA)综合征是导致该病情的原因。观察到右冠状动脉增厚,向左冠状动脉有大量侧支血流。在作者所在的重症监护病房进行初始治疗后,实施了手术干预。患者出院时无任何神经损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8457/11761830/f18495fea4a2/108_2024_1782_Fig1_HTML.jpg

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