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法洛四联症合并肺动脉瓣缺如和肺动脉不融合:一个管理难题。

Tetralogy of Fallot With Absent Pulmonary Valve and Nonconfluent Pulmonary Arteries: A Management Conundrum.

机构信息

Division of Pediatric Cardiology, Department of Pediatrics, Holtz Children's Hospital, Jackson Memorial Medical Center, University of Miami Miller School of Medicine, Miami, FL, USA.

Department of Radiology, Holtz Children's Hospital, Jackson Memorial Medical Center, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2020 Jul;11(4):NP168-NP171. doi: 10.1177/2150135118775661. Epub 2018 Aug 27.

Abstract

Tetralogy of Fallot with absent pulmonary valve syndrome is a rare form of congenital heart disease. Among the different variations with this rare anomaly is nonconfluent pulmonary artery branches with anomalous origin of the left pulmonary artery from the ductus arteriosus. The authors present one such case which was diagnosed prenatally to have tetralogy of Fallot with absent pulmonary valve and identified postnatally to have nonconfluent pulmonary artery branches in addition. We discuss the conundrum of respiratory management in this patient pre- and postoperatively due to a unique ventilation perfusion mismatch problem, which varies between the two lungs.

摘要

法洛四联症合并肺动脉瓣缺如综合征是一种罕见的先天性心脏病。在这种罕见异常的不同变异中,有一种是肺动脉分支未融合,而左肺动脉异常起源于动脉导管。作者报告了这样一个病例,该病例在产前被诊断为法洛四联症合并肺动脉瓣缺如,并在产后发现除了法洛四联症外,还有肺动脉分支未融合。我们讨论了由于两个肺之间存在独特的通气-灌注不匹配问题,该患者在术前和术后的呼吸管理难题。

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