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法洛四联症中肺动脉变异及其他相关缺陷

Variations of pulmonary arteries and other associated defects in Tetralogy of Fallot.

作者信息

Sheikh Abdul Malik, Kazmi Uzma, Syed Najam Hyder

机构信息

Department of Paediatric Cardiology, The Children Hospital and The Institute of Child Health, Ferozpur Road, Lahore, Punjab, Pakistan.

出版信息

Springerplus. 2014 Aug 26;3:467. doi: 10.1186/2193-1801-3-467. eCollection 2014.

Abstract

BACKGROUND

The objective of study was to determine pulmonary artery variations and other associated cardiac defects in patients with Tetralogy of Fallot. This cross-sectional, descriptive study was carried out at The Children's Hospital and the Institute of Child Health, Lahore, from January 2006 to December 2012. All patients with Tetralogy of Fallot, who underwent cardiac catheterization during this period, were included. Standard cine-angiograms were done to record the pulmonary artery sizes and associated cardiac defects.

DESCRIPTION

A total of 576 patients with Tetralogy of Fallot were catheterized. Pulmonary Artery abnormalities were present in 109 (18.92%) patients. The commonest abnormality was isolated Left Pulmonary Artery stenosis (n = 60, 10.4%) followed by supra-valvular stenosis (n = 9, 1.6%). Left Pulmonary Artery was absent in seven patients(1.2%), while 1 patient (0.2%) had both absent right and left Pulmonary Arteries with segmental branch pulmonary arteries originating directly from Main Pulmonary Artery. Associated cardiac lesions included right aortic arch in 72 (12.5%), additional muscular Ventricular Septal Defect in 31 (5.4%), Patent Ductus Arteriosus in 31 (5.4%), bilateral Superior Vena Cava 36(6.2%), Atrial Septal Defect 4(0.7%) and Major Aortopulmonary Collateral Arteries in 75(13%) patients. Significant coronary artery abnormalities were present in 28(4.9%) children.

CONCLUSION

Pulmonary artery abnormalities were present in 18.92% of patients with Tetralogy of Fallot. Isolated Left Pulmonary Artery origin stenosis was the most common abnormality. Significant associated cardiac lesions including Patent Ductus Arteriosus , additional muscular Ventricular Septal Defect, coronary artery abnormalities, bilateral Superior Vena Cava, Atrial Septal Defect and Major Aortopulmonary Collateral Arteries were present in one-third of the patients.

摘要

背景

本研究的目的是确定法洛四联症患者的肺动脉变异及其他相关心脏缺陷。这项横断面描述性研究于2006年1月至2012年12月在拉合尔儿童医院和儿童健康研究所开展。纳入在此期间接受心导管检查的所有法洛四联症患者。进行标准电影血管造影以记录肺动脉大小及相关心脏缺陷。

描述

共有576例法洛四联症患者接受了心导管检查。109例(18.92%)患者存在肺动脉异常。最常见的异常是孤立性左肺动脉狭窄(n = 60,10.4%),其次是瓣上狭窄(n = 9,1.6%)。7例患者(1.2%)左肺动脉缺如,1例患者(0.2%)左右肺动脉均缺如,节段性分支肺动脉直接起源于主肺动脉。相关心脏病变包括右位主动脉弓72例(12.5%)、额外肌部室间隔缺损31例(5.4%)、动脉导管未闭31例(5.4%)、双侧上腔静脉36例(6.2%)、房间隔缺损4例(0.7%)以及主-肺动脉侧支动脉75例(13%)。28例(4.9%)儿童存在显著冠状动脉异常。

结论

18.92%的法洛四联症患者存在肺动脉异常。孤立性左肺动脉起始部狭窄是最常见的异常。三分之一的患者存在显著相关心脏病变,包括动脉导管未闭、额外肌部室间隔缺损、冠状动脉异常、双侧上腔静脉、房间隔缺损以及主-肺动脉侧支动脉。

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