法洛四联症合并肺动脉瓣缺失综合征并左肺动脉缺失-一种罕见的表现

A. Shamsuddin, P. Biswas, Muhammad Ishtiaque Sayeed Al Manzoo, M. Azad, Md Nurul Akhtar Hasan, Jasmin Hosain, Mohammad Sharifuzzaman Shamsuddin
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引用次数: 1

摘要

左肺动脉缺失伴法洛四联症(TOF)合并肺动脉瓣缺失综合征(APVS)是一种罕见的先天性心脏异常。在这里,我们提出这样一个2岁11个月的女孩与紫绀,用力呼吸困难。超声心动图和CT血管造影证实了她的诊断。迄今为止报道的病例很少,术后死亡率高。尽管每次手术决策都是关于肺动脉瓣和RPA大小的挑战,但我们成功地进行了ICR和RPA复位成形术并创建了单尖瓣肺动脉瓣。由于这是一种罕见的关联,我们已经克服了我们在手术中遇到的障碍,我们报告了这个病例。孟加拉国心脏杂志2020;35(1): 74-77
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tetralogy of Fallot with Absent Pulmonary Valve Syndrome with Absent Left Pulmonary Artery - A Rare Presentation
Absent left pulmonary artery with Tetralogy of Fallot (TOF) with absent pulmonary valve syndrome (APVS), is a rare congenital cardiac anomaly. Here we present such a case of A 2 year 11 month old girl with cyanosis, exertional dyspnoea. Her diagnosis is confirmed by echocardiography and CT angiogram. There are very few cases have been reported till date with high postoperative mortality. Although per operative decision making was challenging regarding pulmonary valve and size of the RPA, we performed ICR with RPA reductionplasty and creation of monocuspid pulmonary valve with success. As it is a rare association and we have overcome the hindrance we came across per operatively, we are reporting this case. Bangladesh Heart Journal 2020; 35(1) : 74-77
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