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[二尖瓣闭锁合并正常主动脉瓣及肺动脉闭锁。一例由体循环肺动脉进行肺侧支血管灌注的病例]

[Mitral valve atresia with normal aortic valve and pulmonary atresia. A case with pulmonary collateral vascular perfusion by systemic pulmonary arteries].

作者信息

Hofbeck M, Singer H, Taylor J F

机构信息

Abteilung für Kardiologie, Universität Erlangen-Nürnberg.

出版信息

Herz. 1987 Dec;12(6):413-8.

PMID:3428846
Abstract

A case of mitral atresia with normal aortic valve, situs solitus, d-loop, ASD, VSD, DORV and atresia of the pulmonary valve is presented. Systemic-pulmonary collateral arteries were the single source of collateral lung perfusion. These vessels are often found in patients with tetralogy of Fallot and pulmonary atresia with VSD. The case favours the idea that these vessels are not specific for the above mentioned cardiac anomalies. It supports the theory that they represent true embryonal vessels which can persist in cases of an inadequate or completely missing connection of the sixth aortic arch derivates with the pulmonary vascular bed.

摘要

本文报告一例二尖瓣闭锁合并主动脉瓣正常、心房正位、心室右袢、房间隔缺损、室间隔缺损、右心室双出口及肺动脉瓣闭锁的病例。体肺侧支动脉是肺灌注的唯一侧支来源。这些血管常见于法洛四联症和室间隔缺损合并肺动脉闭锁的患者。该病例支持以下观点,即这些血管并非上述心脏畸形所特有。它支持这样一种理论,即它们代表真正的胚胎血管,在第六主动脉弓衍生物与肺血管床连接不足或完全缺失的情况下可持续存在。

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