CLINICOPATHOLOGICAL CORRELATIONS IN CONGENITAL HEART-SURGERY - THE SURGICAL ANATOMY OF TETRALOGY OF FALLOT WITH PULMONARY ATRESIA RATHER THAN PULMONARY STENOSIS

被引:20
作者
ANDERSON, RH
DEVINE, WA
DELNIDO, P
机构
[1] Divisions of Cardiology, Cardiac Surgery and Pathology, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania
关键词
D O I
10.1111/j.1540-8191.1991.tb00562.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We examined the pertinent surgical features of the anatomy of 56 hearts having tetralogy of Fallot with pulmonary atresia instead of stenosis, or malformations with pulmonary atresia closely related to tetralogy. We took particular cognizance of the pulmonary arterial supply in 15 hearts in which this was derived through systemic-to-pulmonary collateral arteries, dissecting, as far as possible, the bronchopulmonary segmental distribution of the collateral arteries compared to the intrapericardial pulmonary arteries in 11 of these hearts. Two of the hearts had absence of intrapericardial pulmonary arteries, so that a solitary arterial trunk left the base of the heart. Evidence of an atretic subpulmonary infundibulum was found in 40 of the hearts, while such an infundibulum was lacking in the remainder. The pulmonary atresia was muscular in 43 hearts, valvar in 11, while the pulmonary trunk was absent in the other two hearts. In the hearts with collateral arteries, on average 2.6 collaterals were found in each case, varying from two to five per case. Only one of these arose from a brachiocephalic artery, the others all arising from the descending aorta. The distribution of collateral arteries in two cases was remarkably reminiscent of the arrangement of bronchial arteries. As far as could be judged, 16.5 bronchopulmonary segments on average were supplied in each heart, 5.1 exclusively by collateral arteries, 11.8 by intrapericardial pulmonary arteries and an average of 0.64 segments per case having a shared supply.
引用
收藏
页码:41 / 59
页数:19
相关论文
共 22 条
[1]  
Alfieri O, Blackstone EH, Kirklin JW, Et al., Surgical treatment of tetralogy of Fallot with pulmonary atresia, J Thorac Cardiovasc Surg, 76, (1978)
[2]  
Puga FJ, Leoni FE, Julstrud PR, Et al., Complete repair of pulmonary atresia, ventricular septal defect, and severe peripheral arborization abnormalities of the oentral pulmonary arteries. Experience with preliminary unifocalization procedures in 38 patients, J Thorac Cardiovasc Surg, 98, (1989)
[3]  
Matsuda H, Hirose H, Nakano S, Et al., Management of large aortopulmonary collateral arteries in patients with ventricular septal defect and pulmonary atresia: Simultaneous ligation through median sternotomy during intracardiac repair, Ann Thorac Surg, 40, (1985)
[4]  
Barbero-Marcial M, Rizzo A, Et al., New techniques for correction of pulmonary atresia with ventricular septal defect and severe vascular anomalies, Perspectives in Pediatric Cardiology Volume 2 Pediatric Cardiac Surgery Part 1. Mount Kisco, (1989)
[5]  
Haworth SG, Macartney FJ, Growth and development of pulmonary circulation in pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries, Br Heart J, 44, (1980)
[6]  
Thiene G, Bortolotti U, Gallucci V, Et al., Pulmonary atresia with ventricular septal defect, Br Heart J, 39, (1977)
[7]  
Rabinovitch M, deLeon Herrera V, Et al., Growth and development of the pulmonary vascular bed in patients with tetralogy of Fallot with or without pulmonary atresia, Circulation, 64, (1981)
[8]  
Liao PK, Edwards WD, Julstrud PR, Et al., Pulmonary blood supply in patients with pulmonary atresia and ventricular septal defect, J Am Coll Cardiol, 6, (1985)
[9]  
Griffin ML, Sullivan ID, Anderson RH, Et al., Doubly committed subarterial ventricular septal defect: New morphological criteria with echocardiographic and angiocardiographic correlation, Br Heart J, 59, (1988)
[10]  
Marino B, Calabro R, Gagliardi MG, Et al., Patterns of pulmonary arterial anatomy and blood supply in complex congenital heart disease with pulmonary atresia, J Thorac Cardiovasc Surg, 94, (1987)