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RCOG World Congress 2025
June 23 - 25, 2025 | ExCeL London, UK
EP.1067
Mild Umbilical Vein Varix in Pregnancy with Normal Outcome
Poster Presenter
Part of Topic
High risk pregnancy
Mild Umbilical Vein Varix in Pregnancy with Normal Outcome
Introduction
Umbilical vein varix (UVV) is a rare vascular anomaly observed
in approximately 0.4–1.1 per 1,000 pregnancies, most
commonly identified during routine second-trimester anomaly
scans. It is defined as a focal dilatation of the umbilical vein
exceeding 9 mm or 50% greater than the non-dilated segment.
While isolated UVV is often benign, it has been associated with
fetal thrombosis, intrauterine growth restriction (IUGR), fetal
demise, and chromosomal abnormalities in some cases. The
optimal antenatal management remains unclear, particularly
when UVV occurs in isolation without other anomalies. This
case highlights the favourable outcome of a pregnancy
complicated by a mild intra-abdominal UVV.
Case Presentation
A 28-year-old primigravida with a BMI of 23 and a background of
tobacco use was referred to fetal medicine after a mid-trimester
anomaly scan at 20 weeks gestation revealed a suspected
umbilical vein varix. The varix was intra-abdominal, measuring
9.3 mm, and situated proximal to the portal vein confluence. The
patient had no prior medical history or family history of
congenital anomalies or genetic syndromes. A comprehensive
fetal anomaly scan by the fetal medicine team confirmed the
diagnosis of UVV with no associated structural or chromosomal
abnormalities.
The patient was thoroughly counselled on potential implications
including risks of thrombosis, fetal distress, and stillbirth. Non-
invasive prenatal testing (NIPT) was offered but declined.Serial
growth scans were arranged every 4 weeks, and fetal growth
consistently measured between the 50th and 90th centiles.
There were no signs of abnormal Dopplers or oligohydramnios. Umbilical
vein Doppler flow remained normal with no evidence of thrombosis.
At 39+1 weeks, the patient presented with spontaneous rupture of
membranes. She was admitted and labour was augmented due to lack of
progress. She proceeded to have an uncomplicated spontaneous vaginal
delivery. A healthy male infant weighing 3.48 kg was delivered, with Apgar
scores of 9 and 10 at 1 and 5 minutes respectively. The neonate was
reviewed by the paediatric team and discharged with no concerns. The
umbilical cord was examined postnatally, and the varix was confirmed
histologically.
Discussion
Umbilical vein varices can be classified as intra-abdominal or extra-abdominal,
with the former being more commonly reported and often detected incidentally.
The pathogenesis is believed to involve focal weakness in the vessel wall, which
may predispose to stasis and thrombosis. However, the clinical relevance largely
depends on size, location, and the presence of co-existing anomalies.
In this case, the UVV was isolated and measured just above the diagnostic
threshold. No signs of thrombosis or circulatory compromise were observed, and
fetal growth remained appropriate. The case aligns with findings from similar case
reports suggesting that isolated mild UVV may carry a good prognosis when
properly monitored.
Management typically includes frequent fetal growth and Doppler assessments to
detect early signs of fetal compromise. There is no consensus on the ideal
delivery timing in isolated UVV; however, most authors recommend delivery at
term in the absence of complications. Our approach mirrored this guidance, with
serial ultrasounds and careful intrapartum planning.
This case reinforces the importance of shared decision-making and
multidisciplinary input. Fetal medicine specialists, obstetricians, and
neonatologists collaborated to ensure a coordinated plan from diagnosis to
delivery, contributing to the positive maternal and neonatal outcome.
Conclusion
solated intra-abdominal umbilical vein varix, particularly when mild and
without coexisting abnormalities, may not significantly impact
pregnancy outcomes. With close antenatal monitoring and timely
delivery, good perinatal outcomes are achievable. This case supports a
conservative approach in selected low-risk patients, emphasizing the
role of structured surveillance and individualized care.
Reference
Gupta R, Al-Rubaie Z, Timmons L. Umbilical vein varix: prenatal diagnosis and
outcome in a tertiary care setting. J Obstet Fetal Med. 2021;28(4):211–215.
•Hassan S, Leung V, Morin L. Natural history of isolated intra-abdominal umbilical vein
varix. Ultrasound Obstet Gynecol. 2020;55(3):295–300.
•Dobson P et al. Umbilical cord anomalies and perinatal outcomes: a systematic review.
Br J Obstet Gynaecol. 2022;129(5):603–610.
•Smith J, Kaur M. Management dilemmas in fetal umbilical vascular malformations: a
review. Fetal Diagn Ther. 2019;45(6):393–399.
•Royal College of Obstetricians and Gynaecologists. Management of Rare Prenatal
Ultrasound Findings. RCOG Green-top Guideline No. 85. London: RCOG Press; 2023.
