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Oya Demirci, Güher Bolat, Mucize Özdemir, Ayşenur Celayir

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Presentation on theme: "Oya Demirci, Güher Bolat, Mucize Özdemir, Ayşenur Celayir"— Presentation transcript:

1 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

2 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

3 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.

4 Amniotic fluid digestive enzyme activities
gamma-glutamyl transpeptidase (GGTP) value : At the 10 th percentile Intestinal alkaline phosphatase : Low value.

5 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

6 Conclusion Non-visualization of the fetal gallbladder Associated with:
Gallbladder agenesis Biliary atresia Cystic fibrosis Chromosomal abnormalities

7 Genetic consultation Amniocentesis for fetal karyotyping Screening for a CFTR gen mutation Analysis of digestive enzymes GGTP and intestinal alkaline phosphatase

8 Before 22 weeks' gestation
Low amniotic fluid digestive enzyme activities →Biliary atresia After 22 weeks’ gestation Low amniotic fluid digestive enzyme activities →Physiological

9 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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