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DOI 10.1002/pd.456

Медицинская библиотека · Prenatal diagnosis · 2002

Prenatal diagnosis of ductus venosus agenesis and its association with cytogenetic/congenital anomalies.

Volpe Paolo, Marasini Maurizio, Caruso Gilda, Lituania Mario, Marzullo Andrea, Volpe Gennaro, Gentile Mattia

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

We present an observational study of 12 cases of anomalies of the umbilical and portal vein systems associated with absence of the ductus venosus (DV) diagnosed over the past 5 years. The hemodynamic implications of each pattern of umbilico-portal system anomalies associated with absence of the DV have been investigated, as well as the frequency and types of associated anomalies and their embryological origin.

METHODS

In all cases ultrasound, color Doppler, and cytogenetic investigations were performed.

RESULTS

Four main patterns of abnormal venous circulation were documented: (1). the umbilical vein (UV) bypasses the liver and drains into the right atrium directly or through a dilated coronary sinus (three cases); (2). the UV bypasses the liver, with an infrahepatic or suprahepatic connection directly to the inferior vena cava (IVC) (two cases); (3). the UV bypasses the liver and drains directly into the iliac or renal veins (four cases); and (4). the UV drains directly into the portal veins (three cases). Among seven cases with other associated anomalies (58%), there were three cases of Turner's and Noonan's syndromes. Two fetuses and two neonates died and there were two terminations of pregnancy (TOP).

CONCLUSIONS

In utero diagnosis of ultrasound patterns associated with DV anomalies is feasible. Fetal karyotyping should be considered, serial ultrasound examinations recommended and, in the presence of heart failure, delivery can be anticipated.

Для цитирования: Volpe Paolo, Marasini Maurizio, Caruso Gilda, Lituania Mario, Marzullo Andrea, Volpe Gennaro, Gentile Mattia. Prenatal diagnosis of ductus venosus agenesis and its association with cytogenetic/congenital anomalies.. Prenatal diagnosis. 2002. DOI: 10.1002/pd.456.

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