医学
肺动脉
左冠状动脉
无症状的
心脏病学
左肺动脉
动脉
内科学
怀孕
右肺动脉
胎儿
心源性猝死
右冠状动脉
心肌梗塞
冠状动脉造影
生物
遗传学
作者
Huan Wang,Zhipan Liang,Gen Zhang,Haibing Fang,Dianyuan Li
出处
期刊:Heart Surgery Forum
[Carden Jennings Publishing Co.]
日期:2023-09-20
卷期号:26 (5): E441-E448
摘要
An anomalous left coronary artery originating from the pulmonary artery (ALCAPA) refers to the abnormal origin of the left coronary artery either from the main pulmonary artery, pulmonary artery sinus, or the left and right pulmonary arteries, with the main pulmonary artery or pulmonary artery sinus being the most common sites. If not diagnosed and treated promptly, this condition can result in death within the first year of life in 90% of patients. Asymptomatic children can survive into adulthood, but they are at a high risk of sudden death. In this article, we report a case of a 24-year-old pregnant woman who was diagnosed with ALCAPA during prenatal examination. The pregnancy was successfully maintained until 36 weeks, after which a cesarean section was performed. The patient was then admitted to the cardiac surgery department to improve cardiac function, and six weeks later, a successful left coronary artery transplantation was performed. The patient was discharged and followed up for three months, during which her condition remained stable.
科研通智能强力驱动
Strongly Powered by AbleSci AI