妊娠早期诊断肺动脉瓣缺失(APV): 1例产前治疗报告,并回顾波兰国家胎儿心脏病理登记处的文献和数据

Prenatal Cardiology Pub Date : 2014-09-01 DOI:10.12847/09143
A. Nawara, Beata Radzymińska-Chruściel, Maria Respondek Liberska, K. Januszewska, E. Malec
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引用次数: 2

摘要

摘要:肺动脉瓣缺失综合征是一种罕见的先天性心脏缺陷,根据波兰国家胎儿心脏异常登记处的数据,先天性心脏缺陷胎儿的产前诊断率为0.8%。我们提出一个病例的孕妇和胎儿与心脏缺陷,这是在妊娠早期发现和治疗地高辛,羊膜还原,胎解和类固醇后,在新生儿期心脏手术。尽管进行了强化治疗,婴儿还是在3个月大时死亡。我们认为结局不佳的主要原因是妊娠第35周早产。我们提出了独特的心脏图像证明这种类型的异常变化的特点,自1孕早期
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First trimester diagnosis of Absent Pulmonary Valve (APV): a case report of prenatal treatment with a review of literature and data from The Polish National Registry of Fetal Cardiac Pathology
Abstract Absent of pulmonary valve syndrome is a rare congenital heart defect, which is diagnosed prenataly in 0,8% of fetuses with congenital heart defect based on the data from National Polish Registry Of Fetal Cardiac Anomalies. We present a case of pregnat woman and fetus with that heart defect, which was detected in the 1st trimester and treated prenatally with digoxin, amnioreduction, tocolysis and steroids following by the cardiac sugery in the neonatal period. Despite an intensive therapy, the infant died on the 3rd month of age. We belive that the main reason of poor outcome was premature delivery at the 35th week of gestation. We present unique cardiac images proving the changing characterists of this type anomay since 1 st trimester
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