Mildner R J, Kiraly L, Sreeram N
Heart Unit, Birmingham Children's Hospital.
Heart. 1997 Feb;77(2):173-5. doi: 10.1136/hrt.77.2.173.
In muscular pulmonary atresia, major aortopulmonary collateral arteries are characteristic of pulmonary atresia with ventricular septal defect and are rarely seen in pulmonary atresia with intact ventricular septum. Two unusual cases of muscular pulmonary atresia are reported, one with an intact septum and one with a perimembranous ventricular septal defect, closed in utero by aneurysmal tricuspid tissue. In both cases the pulmonary blood supply came entirely from aortopulmonary collaterals. In case 1 a collateral artery connected the left subclavian artery and hypoplastic pulmonary arteries, and several aortopulmonary collaterals arose from the descending aorta, without overlap between these two circulations. In case 2 the pulmonary trunk and arterial duct were absent and the pulmonary blood supply came entirely from collateral arteries. The right ventricle was of normal size and tripartite with a closed perimembranous ventricular septal defect, discovered only at postmortem examination. These observations suggest right ventricular outflow tract obstruction early in fetal development, with involution of the pulmonary trunk and sixth arch derivatives, and persistence of primitive aortopulmonary connections. The morphology in case 1 is at odds with the theoretical division of pulmonary atresia with intact septum and pulmonary atresia with ventricular septal defect into two separate pathological entities that occur at different stages in fetal development.
在肌性肺动脉闭锁中,主肺动脉侧支动脉是室间隔缺损型肺动脉闭锁的特征性表现,而在室间隔完整型肺动脉闭锁中则很少见。本文报告了两例不寻常的肌性肺动脉闭锁病例,一例室间隔完整,另一例为膜周部室间隔缺损,在子宫内由动脉瘤样三尖瓣组织闭合。两例病例的肺血供应均完全来自主肺动脉侧支。病例1中,一条侧支动脉连接左锁骨下动脉和发育不全的肺动脉,数条主肺动脉侧支起源于降主动脉,这两个循环之间无重叠。病例2中,肺动脉干和动脉导管缺如,肺血供应完全来自侧支动脉。右心室大小正常,呈三部分结构,膜周部室间隔缺损闭合,仅在尸检时发现。这些观察结果提示,在胎儿发育早期存在右心室流出道梗阻,肺动脉干和第六弓衍生物退化,原始主肺动脉连接持续存在。病例1的形态学表现与将室间隔完整型肺动脉闭锁和室间隔缺损型肺动脉闭锁分为两个在胎儿发育不同阶段出现的独立病理实体的理论划分不一致。