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一例罕见的高位起始右冠状动脉偶然发现:病例报告。

An incidental encounter of a rare high take-off right coronary artery: A case report.

作者信息

Deng Xicheng, Huang Peng, Chen Wenjuan, Yang Xiaohui, Liu Qianjun, Xiao Yunbin, He Cheng

机构信息

Heart Center Department of Ultrasound and Echocardiography, Hunan Children's Hospital, Hunan, China Department of Cardiothoracic Surgery, Alfred Hospital, Melbourne, Victoria, Australia.

出版信息

Medicine (Baltimore). 2017 Nov;96(45):e8614. doi: 10.1097/MD.0000000000008614.

Abstract

RATIONALE

High take-off of the coronary arteries is a rare cardiac anatomic anomaly, which may occur independently or with other congenital heart defects. In the clinical setting, it is noteworthy as a cause of sudden cardiac death. Further, it is vital to identify such anomalies to avoid intraoperative catastrophes in surgeries for congenital heart defects.

PATIENT CONCERNS

A II/6 systolic heart murmur on physical examination was incidentally found in a 9-year-old boy; he was confirmed to have a secundum-type atrial septal defect on echocardiography. He was referred to our institution for elective surgery.

DIAGNOSES

The preoperative echocardiogram confirmed the presence of an atrial septal defect, and during the surgical procedure, a high take-off right coronary artery was found.

INTERVENTIONS

The atrial septal defect was closed surgically, and care was taken to avoid clamping the anomalous right coronary artery when placing the aortic cross-clamp.

OUTCOMES

Postoperative echocardiogram verified the presence of the high take-off right coronary artery and a satisfactory repair of the atrial septal defect. The postoperative course was uneventful, and the patient was discharged on postoperative day 5.

LESSONS

This case suggests that it is critical to perform echocardiography to assess the anatomy of the coronary arteries, especially in pediatric cardiac patients. In addition, multi-detector computed tomography may be considered if appropriate. Care should be taken to assess the coronary anatomy for anomalies during interventional therapy or surgery, especially in congenital cases.

摘要

理论依据

冠状动脉高位起始是一种罕见的心脏解剖异常,可单独出现或与其他先天性心脏缺陷并存。在临床环境中,它作为心源性猝死的一个原因值得关注。此外,识别此类异常对于避免先天性心脏缺陷手术中的术中灾难至关重要。

患者情况

一名9岁男孩在体格检查时偶然发现II/6级收缩期心脏杂音;超声心动图证实他患有继发孔型房间隔缺损。他被转诊至我院进行择期手术。

诊断

术前超声心动图证实存在房间隔缺损,手术过程中发现右冠状动脉高位起始。

干预措施

通过手术闭合房间隔缺损,在放置主动脉交叉钳夹时注意避免钳夹异常的右冠状动脉。

结果

术后超声心动图证实右冠状动脉高位起始存在,房间隔缺损修复满意。术后过程顺利,患者于术后第5天出院。

经验教训

该病例表明,进行超声心动图检查以评估冠状动脉解剖结构至关重要,尤其是在小儿心脏患者中。此外,如有必要可考虑使用多排螺旋计算机断层扫描。在介入治疗或手术期间,尤其是先天性病例,应注意评估冠状动脉解剖结构是否存在异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0341/5690786/81fab105cb37/medi-96-e8614-g001.jpg

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