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Published byLester Henderson Modified over 6 years ago
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Non-visualization of the gallbladder on fetal ultrasound: Prenatal findings and postnatal outcome
Oya Demirci, Güher Bolat, Mucize Özdemir, Ayşenur Celayir Zeynep Kamil Gynecologic and Pediatric Training and Research Hospital, Perinatology Department
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Case 26 years old primigravida woman.
At 22 weeks’ gestation on detailed examination Hyperechogenic fetal bowel was seen. The gallbladder could not be visualized. Amniocentesis was performed at 23 weeks
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Normal karyotype was established.
CFTR gene mutation was not detected. Ƴ-glutamyl transpeptidase and intestinal alkaline phosphatase were investigated. Normal development or bening gallbladder agenesis Severe anomaly such as biliary atresia.
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Amniotic fluid digestive enzyme activities
gamma-glutamyl transpeptidase (GGTP) value : At the 10 th percentile Intestinal alkaline phosphatase : Low value.
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37 weeks, 2780 g female neonate Normal clinical and biochemical findings On postnatal ultrasound examination : The small gallbladder Normal bile duct and common hepatic duct
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Conclusion Non-visualization of the fetal gallbladder Associated with:
Gallbladder agenesis Biliary atresia Cystic fibrosis Chromosomal abnormalities
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Genetic consultation Amniocentesis for fetal karyotyping Screening for a CFTR gen mutation Analysis of digestive enzymes GGTP and intestinal alkaline phosphatase
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Before 22 weeks' gestation
Low amniotic fluid digestive enzyme activities →Biliary atresia After 22 weeks’ gestation Low amniotic fluid digestive enzyme activities →Physiological
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Result Our case, Low intestinal alkaline phosphatase level
Normal bile duct, common hepatic duct This result may be due to Amniosentesis after 22 weeks’ gestation
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