Absence of the ductus venosus is a rare vascular anomaly. We report a late
onset of a hydrops fetalis seen in a fetus at 34 completed weeks of gestati
on. A persistence of the cranial parts of the left and right umbilical vein
s and of the paired cranial vitelline veins with an absent ductus venosus l
ed to a bilateral hydrothorax, ascites and skinedema. Postnatally the hydro
ps resolved within 7 days most probably due to the change from the fetal to
the adult circulation. The abnormal venous system was confirmed by angiogr
aphy. Agenesis of the ductus venosus can manifest in two different morpholo
gic patterns: The umbilical vein drains exclusively into the left branch of
the intrahepatic portal vein or the umbilical vein drains into the inferio
r vena cava or directly into the right atrium by-passing the liver complete
ly. In both patterns, the preferential direction of the flow towards the fo
remen ovale is not present. While the first pattern leads to hyperperfusion
of the liver parenchyma, the latter would result in reduced perfusion and
oxygenation. Our findings suggest that agenesis of ductus venosus might ind
uce hydrops fetalis. We conclude, that in every case of hydrops fetalis the
venous system should be evaluated by ultrasonography prenatally and/or imm
ediately postnatally.