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

Innere Medizin (Heidelberg, Germany) Pub Date : 2025-01-01 Epub Date: 2024-09-20 DOI:10.1007/s00108-024-01782-4
Tim Urban, Sebastian Grundmann, Franziska Klein, Tobias Wengenmayer, Katharina Müller-Peltzer, Hans-Jörg Busch
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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.

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[成年后首次诊断出 ALCAPA 综合征:心脏骤停的罕见病因]。
一名 42 岁的患者在院外心脏骤停后恢复了自主循环(ROSC),被转诊到作者所在的急诊科。最初的心律是心室颤动。计算机断层扫描和随后的冠状动脉造影显示,肺动脉左冠状动脉异常(ALCAPA)综合征是导致这种情况的原因。观察到右冠状动脉增粗,左冠状动脉有明显的侧支血流。在作者所在的重症监护室进行初步治疗后,进行了手术干预。患者出院时未受到任何神经损伤。
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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