Haworth S G
Br Heart J. 1982 Dec;48(6):513-24. doi: 10.1136/hrt.48.6.513.
To investigate the possibility that pulmonary vascular disease may be present at birth in children presenting with obstructed total anomalous pulmonary venous return in the neonatal period, pulmonary vascular structure was analysed in the lungs of six babies who died during the first week of life. Five babies had infradiaphragmatic total anomalous return and in one the pulmonary veins drained to the right atrium. In all cases mean percentage arterial medial thickness was greater than is normal at 5 hours. The most striking change occurred in the intra- and extrapulmonary veins. Within the lung, in all six cases mean percentage vein wall thickness was significantly increased and in two cases intimal proliferation occurred in preacinar veins. The extrapulmonary veins were generally small in all five cases of infradiaphragmatic total anomalous pulmonary venous return, microscopically were abnormally thick walled in four, and showed intimal proliferation in three cases. In two cases the descending vertical vein was severely narrowed or occluded. A prenatal increase in intrapulmonary arterial and venous muscularity may encourage episodic pulmonary hypertension in the immediate postoperative period. In the infradiaphragmatic type of anomaly, prenatal structural changes in the extrapulmonary veins may predispose to the later development of pulmonary vein stenosis despite a successful surgical repair.
为了研究在新生儿期表现为梗阻性完全性肺静脉异位回流的儿童出生时是否可能存在肺血管疾病,对6例出生后第一周内死亡婴儿的肺脏进行了肺血管结构分析。5例婴儿为膈下型完全性肺静脉异位回流,1例肺静脉引流至右心房。所有病例在出生5小时时动脉中层平均厚度百分比均高于正常。最显著的变化发生在肺内和肺外静脉。在肺内,所有6例病例静脉壁平均厚度百分比均显著增加,2例病例腺泡前静脉出现内膜增生。在5例膈下型完全性肺静脉异位回流病例中,肺外静脉一般较小,4例显微镜下显示壁异常增厚,3例出现内膜增生。2例病例中降垂直静脉严重狭窄或闭塞。产前肺内动脉和静脉肌层增加可能会在术后即刻诱发阵发性肺动脉高压。在膈下型畸形中,尽管手术修复成功,但肺外静脉的产前结构改变可能易导致后期肺静脉狭窄的发生。