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室间隔缺损合并单侧肺动脉狭窄及对侧肺动脉高压

[Combination of ventricular septal defect with unilateral pulmonary artery stenoses and contralateral pulmonary hypertension].

作者信息

Barth H, Schmaltz A A, Steil E, Apitz J

出版信息

Z Kardiol. 1984 Nov;73(11):710-6.

PMID:6543069
Abstract

The clinical features and hemodynamics of the triad ventricular septal defect, unilateral stenoses of the pulmonary artery and contralateral pulmonary hypertension are illustrated by means of 2 case histories. At the time of cardiac catheterization the discovery of severe pulmonary vascular disease of the left lung with inoperable multiple peripheral stenoses of the right pulmonary artery in the first patient, a 4-year old girl, meant that corrective surgery could no longer be undertaken. The second patient, a 10-month old infant with embryofetal alcohol syndrome, suffered from peripheral and two central stenoses of the right pulmonary artery with a total systolic pressure gradient of 62 mm Hg. In our opinion, if the contralateral pulmonary vascular bed has to cope largely single-handed with the increased cardiac output of the right ventricle as a result of additional unilateral pulmonary artery stenosis, the hemodynamic impact of a ventricular septal defect is considerably increased and the development of pulmonary vascular disease accelerated. Since there are strong indications that unilateral pulmonary artery stenosis has more than a mere mechanical effect causing regulative (humorally?, neurogenically?) pulmonary hypertension due also to increased resistance, we are in favour of early closure of the ventricular septal defect and additionally, if technically possible, of an angioplasty or a bypass operation of the stenosis. Since, to the best of our knowledge, an association between proved pulmonary artery stenoses and embryofetal alcohol syndrome has not yet been reported, we feel that our findings are worth sharing.

摘要

通过两个病例史阐述了室间隔缺损、单侧肺动脉狭窄和对侧肺动脉高压三联征的临床特征及血流动力学情况。在心脏导管插入术时,第一位患者是一名4岁女孩,发现左肺存在严重的肺血管疾病且右肺动脉有无法手术治疗的多处外周狭窄,这意味着无法再进行矫正手术。第二位患者是一名患有胚胎酒精综合征的10个月大婴儿,右肺动脉存在外周及两处中央狭窄,总收缩压梯度为62毫米汞柱。我们认为,如果由于额外的单侧肺动脉狭窄,对侧肺血管床不得不主要独自应对右心室增加的心输出量,那么室间隔缺损的血流动力学影响会显著增加,肺血管疾病的发展也会加速。由于有充分迹象表明单侧肺动脉狭窄不仅具有单纯的机械作用,还会因阻力增加导致调节性(体液性?神经性?)肺动脉高压,我们赞成早期关闭室间隔缺损,此外,如果技术上可行,还赞成对狭窄进行血管成形术或旁路手术。据我们所知,尚未有已证实的肺动脉狭窄与胚胎酒精综合征之间关联的报道,我们觉得我们的发现值得分享。

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