ArticleRadiology case reports2019
Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease.
Article in Radiology case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 18 citations in OpenAlex.
- Clinical outcomes of liver transplantation in Caroli syndrome: a retrospective analysis.Orphanet journal of rare diseases · 2025Article
- Prenatal diagnosis and molecular characterization ofFrontiers in genetics · 2025Article
- A Unique Case of Caroli Disease in Kenya's Medical Landscape.The American journal of case reports · 2024Article
- Caroli syndrome associated with atrial septal defect and polydactyly: a case report.Journal of medical case reports · 2023Article
- Diagnostic Value and High-Risk Factors of Two-Dimensional Ultrasonography Combined with Four-Dimensional Ultrasonography in Prenatal Ultrasound Screening of Fetal Congenital Malformations.Computational and mathematical methods in medicine · 2022Article
- Autosomal Recessive Polycystic Kidney Disease-The Clinical Aspects and Diagnostic Challenges.Journal of pediatric genetics · 2021Review
- Imaging of fetal cystic kidney disease: multicystic dysplastic kidney versus renal cystic dysplasia.Pediatric radiology · 2020Review
- Diagnostic value of four-dimensional ultrasonography with STIC combined with two-dimensional ultrasonography for fetal cardiac malformation and chromosomal abnormalities in early pregnancy.Experimental and therapeutic medicine · 2020Article
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Caroli syndrome, which is characterized by saccular and fusiform dilatation of the biliary ducts, is usually observed in association with autosomal recessive polycystic kidney disease (ARPKD). Although the diagnosis of ARPKD is generally easy to make in postnatal ultrasound, the diagnosis of Caroli syndrome may be challenging in prenatal ultrasound. Herein, we present a case of a 29-week fetus with ARPKD associated with Caroli syndrome in whom fetal magnetic resonance imaging was essential to identify the "central dot sign" within the dilated biliary ducts to confirm the prenatal diagnosis of Caroli syndrome and to increase our level of confidence in this diagnosis.
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