起源于肺动脉的右冠状动脉异常(ARCAPA):近十年来罕见的表现。

IF 1.1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-03-01 DOI:10.1177/21501351221141437

V Sharma, F Doig, Ryan Maxwell, D Grout, U Saeed, D Wall

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引用次数: 0

摘要

本文报告一名54岁男性耶和华见证会信徒，诊断为右冠状动脉异常，起源于肺动脉主动脉，最初表现为间歇性疲劳、胸痛、心悸和身体虚弱。在升主动脉上再植异常冠状动脉。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Anomalous Right Coronary Artery Originating From the Pulmonary Artery (ARCAPA): A Rare Presentation in the Fifth Decade.

Presented is a case report of a 54-year-old male Jehovah's Witness diagnosed with an anomalous right coronary artery originating from the main pulmonary artery with the initial presentation with a history of episodic fatigue, chest pain, palpitation, and bodily weakness. The patient was managed with reimplantation of the anomalous coronary artery onto the ascending aorta.

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来源期刊

World Journal for Pediatric and Congenital Heart Surgery CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

1.80

自引率

11.10%

发文量

128