TY - JOUR
T1 - Correlation of Prenatal and Postnatal Diagnosis in Umbilical-Portal-Systemic Venous Shunts
AU - Jimenez-Gomez, Javier
AU - Güizzo, Javier Roberto
AU - Alvarenga, Josue Betancourth
AU - Martínez, Saioa Santiago
AU - Perez, Mireia Gaspar
AU - Perez, Silvia Pina
AU - Beltrán, Viviana Patricia
AU - Loverdos, Inés
AU - Miró, Clara Esteva
AU - Arribas, Paula Jimenez
AU - Vazquez, Begoña Sanchez
AU - Vela, Begoña San Vicente
AU - García, Natalia Álvarez
AU - Núñez, Bernardo
PY - 2023/2
Y1 - 2023/2
N2 - Introduction 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. Methods 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. Results 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). Conclusion: 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.
AB - Introduction 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. Methods 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. Results 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). Conclusion: 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.
U2 - 10.1055/s-0042-1760379
DO - 10.1055/s-0042-1760379
M3 - Article
C2 - 36610389
SN - 0939-7248
JO - European Journal of Pediatric Surgery
JF - European Journal of Pediatric Surgery
ER -