Objective: This study aimed to provide insight about clinical management of ciliated hepatic foregut cysts (CHFC) at a tertiary centre.
Background: CHFC is a rare cystic lesion of the liver with malignant potential according to previous reports. However, the current recommendation to resect all cysts in fit patients is based on limited evidence.
Methods: Retrospective observational single-centre study including all patients with radiological suspicion of CHFC at Karolinska University Hospital during the years 2015-2022. Patients were characterised, mainly descriptively, regarding baseline characteristics, radiological and histopathological data, as well as data on follow-up.
Results: A total of 41 patients with suspected CHFC were identified. Of these, 23 were operated and 18 only diagnosed radiologically. Of the operated, 19 patients (83%) had a histopathological examination confirming CHCF diagnosis. No patient had dysplasia or cancer in the specimen, and no patient developed cancer during a follow-up length (from first radiology) of 82 months (3-215).
Conclusions: CHFC can be diagnosed radiologically with acceptable accuracy. No patient in this study had malignant transformation, neither in the specimens nor during follow-up. Surgical treatment of CHCF for all patients fit for surgery should probably be challenged, but further studies supporting this change of management are needed.
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http://dx.doi.org/10.1080/00365521.2025.2465622 | DOI Listing |
Scand J Gastroenterol
February 2025
Department of Clinical Sciences, Karolinska Institutet, Danderyds Hospital, Stockholm, Sweden.
Objective: This study aimed to provide insight about clinical management of ciliated hepatic foregut cysts (CHFC) at a tertiary centre.
Background: CHFC is a rare cystic lesion of the liver with malignant potential according to previous reports. However, the current recommendation to resect all cysts in fit patients is based on limited evidence.
Ciliated hepatic cyst (CHRC) is a rare, benign hepatic lesion characterized by a pseudostratified ciliated epithelium, distinct from intrahepatic bile ducts. First described in 1984, fewer than 80 cases have been reported. These cysts are often asymptomatic and discovered incidentally during imaging.
View Article and Find Full Text PDFJ Hazard Mater
November 2024
College of Marine Life Sciences, Key Laboratory of Evolution & Marine Biodiversity (Ministry of Education) and Institute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, China; MoE Key Laboratory of Evolution and Marine Biodiversity, Ocean University of China, Qingdao 266003, China. Electronic address:
Bull Cancer
March 2025
Service de chirurgie digestive, hépatobiliaire et endocrinienne, hôpital Cochin, AP-HP Centre, université Paris Cité, Paris, France. Electronic address:
Benign tumors of the liver and biliary tract are rare entities, and some of them require surgical management to prevent their malignant transformation. Tumors from the biliary tract with malignant potential are treated either by hepatic resection, for mucinous cystic neoplasm and ciliated hepatic foregut cysts, or by biliary resections, for biliary papillary neoplasm and type I and IV choledochal cysts. The pathologies requiring prophylactic cholecystectomy are polyps larger than 10 mm, porcelain gallbladder and pancreaticobiliary maljunction.
View Article and Find Full Text PDFCureus
August 2023
General Surgery, Yeni Klinika, Baku, AZE.
A ciliated hepatic foregut cyst (CHFC) is a very uncommon cystic hepatic lesion that arises from an embryonic remnant of the foregut epithelium. CHFC is predominantly asymptomatic and is found incidentally. However, it can show various clinical presentations such as pain and weight loss.
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