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[完全性肺静脉异位引流中肺静脉狭窄。是相关异常还是医源性异常?]

[Stenosis of the pulmonary veins in total anomalous pulmonary venous drainage. Associated or iatrogenic abnormality?].

作者信息

Toulemonde V, Sidi D, Kachaner J, Le Bidois J, Cohen L, Guarnera S, Piéchaud J F, Planché C, Vouhé P

机构信息

Service de cardiologie pédiatrique, hôpital Necker-Enfants Malades, Paris.

出版信息

Arch Mal Coeur Vaiss. 1990 May;83(5):633-9.

PMID:2114076
Abstract

Obstruction of total anomalous pulmonary venous drainage (TAPVD) is sometimes observed in neonates, usually at the site where the collector drains into the caval system. Stenosis of the pulmonary veins themselves before joining the collector is less common. This was observed in 6 cases of intra- and supracardiac TAPVD; the prognosis is usually very bad due to postoperative pulmonary hypertension (PHT) which is difficult to treat. Three of our cases had TAPVD into the coronary sinus with obstruction presenting at birth. Conventional surgery did not reduce the PHT of the first 2 children because the congenital stenosis of the pulmonary veins was not corrected. In the first case, the pulmonary veins resembled fibrous cords and in the second case, the collector was stenosed at its junction with the coronary sinus. These two children died despite surgery. The third child, however, was cured because the obstruction was diagnosed preoperatively and successfully treated when the TAPVD was corrected. In the other three cases, TAPVD to the superior vena caval system was not obstructed but the pulmonary veins retracted progressively after surgery causing PHT and right ventricular failure. After unsuccessful percutaneous dilatation, reoperation revealed obstruction due to exuberant scar tissue with retraction at the site of anastomosis and (or) reconstruction of the pulmonary veins by incision or enlargement with a pericardial patch. One of these children survived after pneumonectomy of the obstructed lung which relieved reflex PHT of the contralateral lung.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

新生儿有时会出现完全性肺静脉异位引流(TAPVD)梗阻,通常发生在肺静脉总干汇入腔静脉系统的部位。肺静脉在汇入总干之前自身狭窄较少见。在6例心内型和心上型TAPVD中观察到这种情况;由于术后难以治疗的肺动脉高压(PHT),预后通常很差。我们的3例病例为TAPVD引流至冠状窦,出生时即出现梗阻。前2例患儿接受传统手术未能降低PHT,因为肺静脉先天性狭窄未得到纠正。第1例中,肺静脉类似纤维索条;第2例中,总干在与冠状窦交界处狭窄。这2例患儿尽管接受了手术仍死亡。然而,第3例患儿治愈了,因为术前诊断出梗阻并在纠正TAPVD时成功进行了治疗。另外3例病例中,TAPVD引流至上腔静脉系统未梗阻,但术后肺静脉逐渐回缩,导致PHT和右心室衰竭。经皮扩张失败后,再次手术发现梗阻是由于吻合口和(或)肺静脉重建部位的吻合口处有大量瘢痕组织回缩,通过心包补片切开或扩大来处理。其中1例患儿在切除梗阻肺叶后存活,这缓解了对侧肺的反射性PHT。(摘要截断于250字)

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