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先天性肺动脉瓣缺如合并肺动脉狭窄、动脉导管未闭及室间隔完整。病例报告。

Congenital absence of the pulmonary valve associated with pulmonary stenosis, large ductus arteriosus and intact ventricular septum. Case report.

作者信息

Yurdakul Y, Atasoy S, Sariosmanoğlu N, Ozer S, Bilgiç A

机构信息

Departments of Thoracic and Cardiovascular Surgery, Hacettepe University Faculty of Medicine, Ankara.

出版信息

Turk J Pediatr. 1994 Apr-Jun;36(2):163-9.

PMID:8016919
Abstract

A six-day-old neonate was diagnosed with a severe form of the syndrome of absent pulmonary valve associated with pulmonary stenosis, aneurysmal dilatation of the pulmonary artery and rare findings including an intact ventricular septum and large ductus arteriosus. The patient underwent surgical repair by closed technique. Cardiac catheterization data, hemodynamic and clinical findings, and surgical technique are reported. Congenital absence of the pulmonary valve is a rare cardiac anomaly. An especially severe form occurs with ventricular septal defect and pulmonary stenosis. The usual findings are respiratory distress, aneurysmal dilatation of the pulmonary arteries and pulmonary stenosis.

摘要

一名6日龄新生儿被诊断患有严重形式的肺动脉瓣缺如综合征,伴有肺动脉狭窄、肺动脉瘤样扩张,罕见的表现包括室间隔完整和动脉导管粗大。该患者通过闭式技术接受了手术修复。报告了心导管检查数据、血流动力学和临床发现以及手术技术。先天性肺动脉瓣缺如是一种罕见的心脏异常。一种特别严重的形式伴有室间隔缺损和肺动脉狭窄。常见表现为呼吸窘迫、肺动脉瘤样扩张和肺动脉狭窄。

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