医学
静脉导管
胎儿
胎龄
产前诊断
胎儿超声心动图
脐静脉
脐动脉
产科
门体分流术
回顾性队列研究
单脐动脉
妊娠期
宫内生长受限
怀孕
门脉高压
儿科
心脏病学
内科学
肝硬化
生物化学
遗传学
化学
体外
生物
作者
J Jiménez Gómez,Javier Roberto Güizzo,Josue Betancourth Alvarenga,S Santiago Martínez,M Gaspar Pérez,Sílvia Pina Pérez,Viviana Patricia Beltrán,Inés Loverdos,C Esteva Miró,Paula Jimenez Arribas,Begoña Sanchez Vazquez,B San Vicente Vela,N Álvarez García,B Núñez García
出处
期刊:European Journal of Pediatric Surgery
[Georg Thieme Verlag KG]
日期:2023-01-07
卷期号:33 (01): 090-095
被引量:2
标识
DOI:10.1055/s-0042-1760379
摘要
Umbilical-portal-systemic venous shunts (UPSVS) are rare anomalies in the development of the fetal venous system. There are several postnatal and prenatal classifications of hepatic venous anomalies but the link between them is missing. We aimed to review the prenatal to postnatal diagnosis correlation in UPSVS at our center. It is a retrospective study of patients diagnosed with UPSVS between 2019 and 2021 at our institution. Demographic, obstetric, genetic, and neonatal data were reviewed with special focus on prenatal and postnatal ultrasounds. A total of seven patients were diagnosed with UPSVS at a median of 24 (20-34) weeks of gestational age. All patients were male and 62% were Caucasian. None of the patients had chromosomopathies or cardiac anomalies. One patient had renal ectopia, another one had a single umbilical artery, and a third one suffered from intrauterine growth retardation. An umbilico-systemic shunt (USS) was found in two patients and a ductus venosus-systemic shunt (DVSS) in the rest. Patients with USS were diagnosed postnatally with intrahepatic portosystemic shunts. One of the DVSS patients was transferred to another hospital and the other four had normal postnatal cardiac ultrasounds, with normal abdominal ultrasounds in two patients and lack of postnatally abdominal control in the other two. All babies were found to be doing well at a median follow-up of 1 month (0-24). There is a knowledge gap in the natural history of UPSVS between fetal and neonatal life. Building bridges between prenatal and postnatal research is mandatory in order to understand these rare anomalies.
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