Prenatal diagnosis of two intrahepatic portosystemic shunts associated with absence of ductus venosus

2020 ◽  
Vol 55 (6) ◽  
pp. 845-847
Author(s):  
R. Bardin ◽  
M. Shapira‐Rotman ◽  
O. Konen‐Cohen ◽  
Y. Mozer‐Glassberg ◽  
E. Bruckheimer ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Ductus Venosus ◽  
Portosystemic Shunts

scholarly journals OP32.09: Prenatal diagnosis of ductus venosus agenesis: anatomic variants, associated anomalies and impact on the postnatal course

2014 ◽  
Vol 44 (S1) ◽  
pp. 141-142
Author(s):  
A. Zamprakou ◽  
A. Geipel ◽  
U. Gembruch ◽  
B.S. Strizek ◽  
I. Gottschalk ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Ductus Venosus ◽  
Associated Anomalies ◽  
Anatomic Variants

OP17.08: Ductus venosus agenesis: prenatal diagnosis and fetoneonatal outcome of 35 cases

2015 ◽  
Vol 46 ◽  
pp. 104-104
Author(s):  
B. Muto ◽  
N. Volpe ◽  
T. Fanelli ◽  
F. Alinovi ◽  
V. De Robertis ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Ductus Venosus

scholarly journals Diagnostic value of systematic ultrasonography for trisomy 18 syndrome in fetuses before 16 weeks gestation

2021 ◽  
Author(s):  
Jie Zhou ◽  
Xiaohui Dai ◽  
Hanmin Liu ◽  
Yiping Li ◽  
Ling Luo ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Birth Rate ◽  
Nuchal Translucency ◽  
Diagnostic Value ◽  
Cystic Hygroma ◽  
Trisomy 18 ◽  
Ductus Venosus ◽  
Research Subjects ◽  
Fetal Ultrasonography ◽  
Cardiac Defects

Abstract Purpose To explore the diagnostic value of systematic fetal ultrasonography for trisomy 18 (T18) syndrome before 16 weeks gestation. Methods A total of 12 fetuses with T18 were selected as research subjects and their nuchal translucency (NT) screening and fetal systematic ultrasonographic images acquired at 11–15 weeks were retrospectively analyzed. Results In the 12 fetuses’ NT screening, ten fetuses showed NT thickening, one showed nuchal cystic hygroma, four showed reversed a-wave ductus venosus flow, and three showed omphalocele. The most common anomalies on the systematic ultrasonography before 16 weeks gestation were cardiac defects (12/12, 100%), omphalocele (4/12, 33.3%), limb anomalies (5/12, 41.7%), and facial anomalies (3/12, 25.0%). Seven of the 12 fetuses had multiple structural malformations: three had two structural malformations (25.0%), three had three structural malformations (25.0%), and one had four structural malformations (8.3%). Conclusion Systematic fetal ultrasonography before 16 weeks gestation can detect most of the structural malformations of T18, effectively shortening the prenatal diagnosis time. It is therefore of great importance for reducing the birth rate of children with T18 and minimizing the physical and mental damage to mothers and their families.

P10.02: Fetal absent ductus venosus associated witht portosystemic shunts

2014 ◽  
Vol 44 (S1) ◽  
pp. 237-237
Author(s):  
R. Rodriguez ◽  
E. Antolin ◽  
H. Beatriz ◽  
J. Encinas ◽  
M. De la Calle ◽  
...  
Keyword(s):  
Ductus Venosus ◽  
Portosystemic Shunts ◽  
Absent Ductus Venosus

Prenatal Diagnosis of Agenesis of Ductus Venosus: A Retrospective Study of Anatomic Variants, Associated Anomalies and Impact on Postnatal Outcome

2017 ◽  
Vol 40 (03) ◽  
pp. 333-339 ◽  
Author(s):  
Brigitte Strizek ◽  
Aikaterini Zamprakou ◽  
Ingo Gottschalk ◽  
Maria Roethlisberger ◽  
Astrid Hellmund ◽  
...  
Keyword(s):  
Retrospective Study ◽  
Prenatal Ultrasound ◽  
Venous System ◽  
Ductus Venosus ◽  
Chromosomal Anomalies ◽  
Portal Venous System ◽  
Associated Anomalies ◽  
Portosystemic Shunts ◽  
Anatomic Variants ◽  
Postnatal Outcome

Abstract Purpose To assess the anatomic variants, associated anomalies and postnatal outcome of fetuses with a prenatally diagnosed agenesis of ductus venosus (ADV). Materials and Methods Retrospective study of 119 cases with agenesis of ductus venosus diagnosed by prenatal ultrasound in two tertiary referral centers from 2006 to 2014. The type and location of the umbilical venous drainage site was noted. Charts were reviewed for associated structural or chromosomal anomalies, pregnancy outcome and postnatal course. Results In 24 cases (20.2 %) ADV was an isolated finding, while 95 cases (79.8 %) had associated anomalies. We identified 84 cases (70.6 %) with intrahepatic and 35 cases (29.4 %) with extrahepatic drainage of the umbilical vein. 58.8 % of neonates were alive at follow-up. There was no statistical association between drainage site and associated anomalies or outcome. Postnatal outcome was determined by the presence and severity of associated anomalies. There was no adverse outcome in the isolated group related to ADV. Overall, there were 6 persistent portosystemic shunts, 3 of them with a spontaneous closure, and one total agenesis of the portal venous system with lethal outcome. Conclusion Postnatal outcome in cases with ADV mainly depends on the presence of associated anomalies. In isolated cases the prognosis is generally good, but neonates with a prenatally diagnosed portosystemic shunt should be followed until its occlusion. Portal venous system agenesis is rare but should be ruled out on prenatal ultrasound.

Prenatal Diagnosis of Abnormal Course of Umbilical Vein and Absent Ductus Venosus – Report of Three Cases

2007 ◽  
Vol 23 (2) ◽  
pp. 136-139 ◽  
Author(s):  
J. Hajdú ◽  
T. Marton ◽  
M. Kozsurek ◽  
B. Pete ◽  
Z. Csapó ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Umbilical Vein ◽  
Ductus Venosus ◽  
Absent Ductus Venosus
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