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

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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Abstract

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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起源于肺动脉的右冠状动脉异常(ARCAPA):近十年来罕见的表现。
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。
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来源期刊
CiteScore
1.80
自引率
11.10%
发文量
128
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