Abstract
Objective: When the fetal gallbladder is not seen at ultrasound (US) scan, to propose a diagnostic method of differentiating fetuses who are healthy or have minor anomalies from fetuses with severe anomalies requiring intensive management. Method: We present four clinical cases illustrating this variability, together with additional examinations: karyotyping, screening for cystic fibrosis mutations, amniotic fluid digestive enzyme activities. Results: The four examples we present-biliary duct atresia, biliary agenesis, gallbladder reveal at birth, and cystic fibrosis-illustrate the difficulties of making both diagnosis and prognosis prenatally when the gallbladder is not visualized. Laboratory assays allowed prenatal management. Conclusion: Failure to visualize the gallbladder prenatally may indicate fetal diseases of highly variable prognosis, but may also sometimes be followed by postnatal visualization in a child free of any disease. Prenatal management could help in defining diagnosis and prognosis. Copyright © 2008 John Wiley & Sons, Ltd.
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Boughanim, M., Benachi, A., Dreux, S., Delahaye, S., & Muller, F. (2008). Nonvisualization of the fetal gallbladder by second-trimester ultrasound scan: Strategy of clinical management based on four examples. Prenatal Diagnosis, 28(1), 46–48. https://doi.org/10.1002/pd.1912
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