Abnormalities of the fetal central veins and umbilico-portal system: prenatal ultrasonographic diagnosis and proposed classification

Citation
R. Achiron et al., Abnormalities of the fetal central veins and umbilico-portal system: prenatal ultrasonographic diagnosis and proposed classification, ULTRASOUN O, 16(6), 2000, pp. 539-548
Citations number
45
Categorie Soggetti
Reproductive Medicine
Journal title
ULTRASOUND IN OBSTETRICS & GYNECOLOGY
ISSN journal
09607692 → ACNP
Volume
16
Issue
6
Year of publication
2000
Pages
539 - 548
Database
ISI
SICI code
0960-7692(200011)16:6<539:AOTFCV>2.0.ZU;2-4
Abstract
Objectives Anomalies of the fetal venous system are poorly documented and t heir pathogenesis is not well understood. The present study was undertaken to review the spectrum of fetal central veins and umbilico-portal system an omalies, and to propose a classification system. Methods A 7-year restrospective survey was conducted. Results Nineteen fetuses showed abnormal connection between central veins a nd the fetal heart. Three fetuses showed abnormal connections of the cardin al veins, two of which had interruption of the inferior vena cava, and one had isolated Persistent left superior vena cava. Anomalies of pulmonary vei ns were seen in four fetuses: in two with asplenia syndrome, a vertical con fluent pulmonary artery was observed. In a further two cases total anomalou s pulmonary venous connections were found. Abnormalities of the umbilical v ein (UV) were seen in 10 cases; seven had persistent right UV and three had a spectrum of anomalies: One had abnormal connections of the UV to the lef t iliac vein associated with agenesis of the ductus venosus (DV) and hydrop s fetalis. One case showed in utero occlusion of the DV by echogenic foci t hat resulted in a persistent left proximal UV and porto-systemic shunt. One case had obliteration of the DV secondary to in utero fetal hepatic fibros is. Abnormalities of the vitelline veins or portal system were demonstrated in two cases. One had a left portosystemic shunt which resolved spontaneou sly at 3 months of age, and one had secondary partial occlusion of the left portal system with liver echogenicities and direct communication of the UV with the right atrium. None of the 19 cases had an abnormal karyotype or e vidence of in utero infection. Conclusions Detection of various fetal vein anomalies in utero is feasible. The anomalies vary according to embryologic precursors or etiology. Two ma jor mechanisms seem to be involved in the genesis of fetal vein anomalies: in most cases primary maldevelopment of the venous system occurs, while in the minority secondary, anomalies from possible thromboembolic events or sy stemic disease may play a role.