A case series of prenatal hepatic hilar cyst in the presence of a gallbladder - navigating the dilemma between biliary atresia and choledochal cyst
The spectrum of disease from CC to BA in the setting of a prenatally discovered hepatic hilar cyst is emphasized. Even if cholangiogram differentiates most patients with BA from those with CC, caution is advised for transitional types.
Authors
- Valérie A. McLin (ORCID: https://orcid.org/0000-0002-0711-687X)
- Céline Habre (ORCID: https://orcid.org/0000-0003-2853-4349)
- Ana M. Calinescu (ORCID: https://orcid.org/0000-0002-3813-8991)
- Nathalie Rock (ORCID: https://orcid.org/0000-0001-5315-9267)
- Anne‐Laure Rougemont (ORCID: https://orcid.org/0000-0002-1785-792X)
- Barbara Elisabeth Wildhaber (ORCID: https://orcid.org/0000-0003-4548-382X)
Institutions
- University of Geneva (CH)
- University Hospital of Geneva (CH)
- Geneva College (US)
Publication Details
- Journal
- BMC Pediatrics
- Published
- 2024-09-13
- DOI
- https://doi.org/10.1186/s12887-024-05043-z
- Citations
- 1
- Primary Topic
- Pediatric Hepatobiliary Diseases and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.57
Funders
- Hôpitaux Universitaires de Genève
- Université de Genève