静脉导管发育不全与胎儿畸形4例报告

A. Matias, Diana Pacheco, O. Brandão, N. Montenegro
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For each case, we access the patient’s files in order to extract the following information: gestational age, umbilical vein connection, pre-natal imaging findings, gestational age at delivery or at pregnancy termination, fetal outcomes, post-natal imaging findings, post-mortem findings and karyotype.Results From the four cases included, two were diagnosed in the first trimester and the other two cases in the second trimester of gestation. Prenatal ultrasound studies revealed an intrahepatic shunt in one case and an extrahepatic shunt in three cases. In one case, the karyotype was not performed, whereas the other three had a normal karyotype. Cardiac anomalies were found in three of the four fetuses. All but one case presented with extracardiac abnormalities. None of the cases developed hydrops. 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摘要

背景:静脉导管发育不全(DVA)是一种罕见的疾病,预后多变,部分依赖于相关疾病的存在。因此,产前评估应包括胎儿循环的仔细检查,特别是脐静脉和门静脉畸形。方法在本研究中,我们描述了在本院诊断的4例DVA病例。对于每个病例,我们访问患者的档案,以提取以下信息:胎龄,脐静脉连接,产前影像学结果,分娩或终止妊娠时的胎龄,胎儿结局,产后影像学结果,尸检结果和核型。结果本组4例中,2例在妊娠早期诊断,2例在妊娠中期诊断。产前超声检查显示肝内分流1例,肝外分流3例。在一个案例中,核型没有进行,而其他三个有一个正常的核型。四个胎儿中有三个发现心脏异常。除一例外,其余病例均表现为心外异常。所有病例均未出现水肿。2例目前存活良好,1例妊娠25周终止妊娠,1例因复杂心脏畸形手术纠正14天死亡。结论临床医生应注意胎儿检查中不同的重要发现,这可能是DVA的指示,当怀疑时,应安排一系列的重新评估,以确定任何畸形。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ductus Venosus Agenesis and Fetal Malformations: Report of Four Cases
Background: The agenesis of the ductus venosus (DVA) is a rare condition with a variable prognosis that relies partly on the presence of associated conditions. Therefore, the prenatal evaluation should include a careful examination of fetal circulation, particularly the umbilical and portal venous malformations.Methods In this study, we describe four cases of DVA diagnosed at our institution. For each case, we access the patient’s files in order to extract the following information: gestational age, umbilical vein connection, pre-natal imaging findings, gestational age at delivery or at pregnancy termination, fetal outcomes, post-natal imaging findings, post-mortem findings and karyotype.Results From the four cases included, two were diagnosed in the first trimester and the other two cases in the second trimester of gestation. Prenatal ultrasound studies revealed an intrahepatic shunt in one case and an extrahepatic shunt in three cases. In one case, the karyotype was not performed, whereas the other three had a normal karyotype. Cardiac anomalies were found in three of the four fetuses. All but one case presented with extracardiac abnormalities. None of the cases developed hydrops. Two cases are currently alive and well, one termination of pregnancy occurred at 25 weeks of gestation and one case died at 14 days during surgical correction of a complex cardiac malformation.Conclusions Clinicians should be aware of different and important findings during the fetal examination, which can be indicative of a DVA, and, when suspected, serial revaluations should be scheduled in order to identify any malformation.
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