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室间隔缺损合并肺动脉闭锁的体肺循环动脉供血:尸检血管造影及组织学研究

Systemic-pulmonary arterial supply in pulmonary atresia with ventricular septal defect: postmortem angiograms and histologic survey.

作者信息

Daliento L, Stritoni P, Chioin R, Frescura C, Thiene G

出版信息

Chest. 1978 Dec;74(6):685-7. doi: 10.1378/chest.74.6.685.

Abstract

Postmortem angiographic and histologic studies of the pulmonary arterial circulation were performed in a patient with pulmonary atresia and a ventricular septal defect. While the left lung was supplied by a closing ductus arteriosus, the right lung was supplied by two systemic pulmonary arteries arising from the descending aorta. The examination disclosed that systemic pulmonary arteries lead into the pulmonary vascular bed and the capillaries of the alveolar walls. According to these observations, such collateral circulation is to be considered functional. The pulmonary vascular bed, supplied by the ductus arteriosus and the stenotic systemic pulmonary artery, showed a thin muscular layer in the small arteries and arterioles. On the contrary, medial hypertrophy and severe intimal proliferation were observed in the pulmonary segments perfused by the other large unobstructed systemic pulmonary artery, thus proving that asymmetric pulmonary vascular disease may complicate the natural history of this malformation.

摘要

对一名患有肺动脉闭锁和室间隔缺损的患者进行了肺动脉循环的尸检血管造影和组织学研究。左肺由闭合的动脉导管供血,而右肺由发自降主动脉的两条体肺动脉供血。检查发现,体肺动脉通向肺血管床和肺泡壁的毛细血管。根据这些观察结果,这种侧支循环应被视为具有功能。由动脉导管和狭窄的体肺动脉供血的肺血管床,在小动脉和微动脉中显示出较薄的肌层。相反,在由另一条通畅的大的体肺动脉灌注的肺段中观察到中层肥厚和严重的内膜增生,从而证明不对称性肺血管疾病可能使这种畸形的自然病程复杂化。

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