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5 个月大婴儿出现不寻常表现并导致致命结局的巨大心腔冠状动静脉瘘:病例报告。

Large cameral coronary artery fistula in a 5 months old infant with unusual presentation and fatal outcome: -case report.

机构信息

Department of Pediatrics and Child Health, School of Medicine, College of Health Sciences Addis Ababa University, Addis Ababa, Ethiopia.

Department of Radiology School of Medicine, College of Health Sciences Addis Ababa University, Addis Ababa, Ethiopia.

出版信息

BMC Pediatr. 2023 Aug 5;23(1):385. doi: 10.1186/s12887-023-04196-7.

Abstract

BACKGROUND

Congenital coronary fistulas (CAFs) are uncommon abnormalities communicating the coronary arteries with the cardiac chambers or portion of the systemic or pulmonary circulation. Over 90% of the cases drain into the right side of the heart with only 3% terminating in the left ventricle. Infants with a large CAFs may develop congestive heart failure.

CASE PRESENTATION

A 5 months old female infant presented with labored breathing and worsening of bluish discoloration of the lips and extremities following a prolonged cry. She had a history of breastfeeding difficulty and noticeable bluish discoloration of the lips and extremities since birth. The infant was wasted and had a fast heart rate, bluish lips, and nail beds with clubbing of fingers and toes. A cardiac murmur was noted during her medical checkup. Chest x-ray showed cardiomegaly. Echocardiography and CT angiography showed large Cameral CAF involving the left main and left anterior descending artery draining into the left ventricle. The tricuspid valve was dysplastic, there was secundum ASD, and VSD with a right to left shunt. The patient developed episode of cyanotic spells after crying excessively following a CT angiographic procedure which culminated in respiratory arrest and her demise. She was managed as a case of hypoxic spells in the ICU before her death.

CONCLUSION

This report unveiled unfamiliar case of Cameral coronary artery fistula with left-to-left shunting, cyanosis, and dysplastic tricuspid valve.

摘要

背景

先天性冠状动脉瘘(CAFs)是一种不常见的异常,它使冠状动脉与心脏腔室或部分体循环或肺循环相通。超过 90%的病例引流至右心,只有 3%的病例终止于左心室。有大瘘的婴儿可能会发展为充血性心力衰竭。

病例介绍

一名 5 个月大的女婴,在长时间哭泣后出现呼吸困难,并出现嘴唇和四肢发绀加重。她有母乳喂养困难的病史,自出生以来嘴唇和四肢就有明显的发绀。婴儿消瘦,心率快,嘴唇发蓝,指甲床有杵状指(趾)。体格检查时发现心脏杂音。胸部 X 线片显示心脏增大。超声心动图和 CT 血管造影显示左主干和前降支的大型心腔 CAF 引流至左心室。三尖瓣发育不良,存在房间隔缺损和室间隔缺损,伴有右向左分流。在 CT 血管造影程序后,由于过度哭泣,患者出现了发绀发作,最终导致呼吸停止和死亡。在她去世前,她在 ICU 被作为缺氧发作进行了治疗。

结论

本报告揭示了一种不常见的左向右分流、发绀和发育不良三尖瓣的心腔冠状动脉瘘病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b18/10403903/ca82fe152283/12887_2023_4196_Fig1_HTML.jpg

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