Harris Birthright Centre for Fetal Medicine, Fetal Medicine Research Institute, King's College Hospital, London, UK.
Department of Congenital Heart Disease, Evelina London Children's Hospital, London, UK.
Prenat Diagn. 2018 Dec;38(13):1055-1061. doi: 10.1002/pd.5388.
To define the associations of a prenatally diagnosed, apparently isolated right aortic arch (RAA) with chromosomal or genetic abnormalities and tracheal compression.
This was a retrospective study of apparently isolated RAA assessed by fetal cardiologists and fetal medicine specialists at Kings College Hospital, London between 2000 and 2017.
The search identified 138 cases of apparently isolated RAA. Invasive testing was performed in 75, and chromosomal or genetic anomalies were identified in 16 (22%), and the most common was 22q11 microdeletion. An aberrant left subclavian artery was seen in 51% of cases. Symptoms of a vascular ring were present in 24 of 97 (25%) children who were reviewed after birth. Bronchoscopy was performed in 33 children, and significant tracheal compression was diagnosed in 28, including 18 of 19 symptomatic and 10 of 14 asymptomatic children.
An apparently isolated RAA is associated with a high incidence of chromosomal or genetic abnormalities and a high incidence of tracheal compression in symptomatic and asymptomatic patients. Prenatal counselling for genetic associations and postnatal airway assessment in the context of the vascular anatomy is recommended.
明确产前诊断的孤立性右位主动脉弓(RAA)与染色体或遗传异常以及气管压迫之间的关联。
这是一项回顾性研究,对 2000 年至 2017 年期间在伦敦国王学院医院由胎儿心脏病专家和胎儿医学专家评估的孤立性 RAA 进行评估。
搜索确定了 138 例孤立性 RAA。对 75 例进行了有创性检查,发现 16 例(22%)存在染色体或遗传异常,最常见的是 22q11 微缺失。51%的病例存在异常的左锁骨下动脉。97 例(25%)出生后接受复查的患儿中有 24 例存在血管环症状。对 33 例患儿进行了支气管镜检查,28 例患儿存在明显的气管压迫,其中 19 例有症状患儿中有 18 例,14 例无症状患儿中有 10 例。
孤立性 RAA 与染色体或遗传异常的发生率较高以及有症状和无症状患者的气管压迫发生率较高相关。建议进行遗传相关性的产前咨询以及血管解剖结构背景下的气道出生后评估。