双腔右心室合并室间隔缺损及先天性肺动脉瓣缺失一例。

IF 1 Q4 RESPIRATORY SYSTEM Clinical Medicine Insights-Circulatory Respiratory and Pulmonary Medicine Pub Date : 2014-03-20 eCollection Date: 2014-01-01 DOI:10.4137/CCRPM.S11174
Georges Khoueiry, Tariq Bhat, Mohmad Tantray, Mustafain Meghani, Nidal Abi Rafeh, Mokhtar Abdallah, Wissam Hoyek
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引用次数: 2

摘要

双室右心室(DCRV)是一种罕见的先天性心脏疾病,涉及两个不同的右心室(RV)压力室,通常与室间隔缺损(VSD)相关。通常,梗阻是由从室间隔穿过右心室到右心室游离壁的异常肌束引起的。我们报告一例双室右心室合并室间隔缺损和先天性肺动脉瓣缺失,这是一种罕见的先天性肺漏斗狭窄。除了室间隔缺损外,我们的患者还有先天性肺动脉瓣缺失,这是非常罕见的,据我们所知从未有过报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A rare case of double-chambered right ventricle associated with ventricular septal defect and congenital absence of the pulmonary valve.

Double-chambered right ventricle (DCRV) is a rare congenital heart disorder involving 2 different right ventricle (RV) pressure compartments that is often associated with ventricular septal defect (VSD). Usually, the obstruction is caused by an anomalous muscle bundle crossing the RV from the interventricular septum to the RV free wall. We are reporting a case of double-chambered right ventricle associated with ventricular septal defect and congenital absence of the pulmonary valve, a rare form of congenital infundibular pulmonary stenosis. In addition to ventricular septal defect, our patient had congenital absence of the pulmonary valve, which is very unusual and has never been reported to our knowledge.

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CiteScore
4.20
自引率
0.00%
发文量
9
审稿时长
8 weeks
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