Eur J Pediatr Surg 2023; 33(01): 090-095
DOI: 10.1055/s-0042-1760379
Original Article

Correlation of Prenatal and Postnatal Diagnosis in Umbilical-Portal-Systemic Venous Shunts

Javier Jimenez-Gomez
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Javier Roberto Güizzo
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Josue Betancourth Alvarenga
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Saioa Santiago Martínez
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Mireia Gaspar Perez
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Silvia Pina Perez
2   Department of Obstetrics and Gynecology, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Viviana Patricia Beltrán
3   Department of Radiology, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Inés Loverdos
4   Deparment of Pediatrics, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Clara Esteva Miró
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Paula Jimenez Arribas
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Begoña Sanchez Vazquez
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Begoña San Vicente Vela
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
Natalia Álvarez García
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
,
1   Department of Pediatric Surgery, Hospital de Sabadell, Sabadell, Barcelona, Spain
› Author Affiliations
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Abstract

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.



Publication History

Received: 03 June 2022

Accepted: 04 November 2022

Article published online:
07 January 2023

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