1.Introduction to the recommendations from the European Association for the Study of the Liver clinical practice guidelines on the management of cystic liver disease.
Chen LIANG ; Su Jun ZHENG ; Zhong Ping DUAN
Chinese Journal of Hepatology 2022;30(9):931-933
The diagnosis of cystic liver disease has made great progress with the advent of enhanced imaging techniques. At the same time, its management has gradually improved over the past few decades, providing the basis for the development of appropriate diagnostic and treatment guidelines. To this end, the European Association for the Study of the Liver has developed clinical guidelines for the diagnosis and treatment of non-infectious cystic liver disease. This guideline put forward recommendations based on an in-depth review of the relevant literature for addressing clinical issues, including the diagnosis and treament of hepatic cysts, hepatic mucocystic tumors, biliary hamartomas, polycystic liver disease, Caroli disease or Caroli syndrome, biliary hamartomas, and peribiliary cyst.
Humans
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Liver Diseases/pathology*
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Cysts/pathology*
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Caroli Disease/diagnosis*
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Liver Neoplasms/therapy*
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Hamartoma
3.Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant.
Jeong Tae KIM ; Yoon Jeong HUR ; Jee Min PARK ; Myung Joon KIM ; Young Nyun PARK ; Jae Seung LEE
Yonsei Medical Journal 2006;47(1):131-134
Caroli's syndrome is a rare congenital disorder that involves intrahepatic bile duct ectasia and congenital hepatic fibrosis, frequently seen with concomitant autosomal recessive polycystic kidney disease (ARPKD). Literature on infants with ARPKD is rare. Here, we present a case of a two month old boy who was diagnosed with Caroli's syndrome and ARPKD.
Polycystic Kidney, Autosomal Recessive/complications/*diagnosis/pathology
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Male
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Kidney/ultrasonography
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Infant
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Humans
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Hepatic Duct, Common/pathology/ultrasonography
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Caroli Disease/complications/*diagnosis/pathology
4.A Case of Simple Type Caroli's Disease Confined to Right Lobe of the Liver.
Ho KIL ; Eun Young CHOI ; Jee In JEONG ; Chan Sun PARK ; Seon Mee PARK ; Seok Hyung KIM ; Kil Sun PARK ; Lee Chan JANG
The Korean Journal of Gastroenterology 2007;50(4):271-276
Caroli's disease is a rare congenital hepatobiliary disease characterized by multifocal segmental dilatation of intrahepatic bile ducts affecting all or parts of the liver. Two forms of Caroli's disease are described, the pure form and that associated with periportal fibrosis. The disease may diffusely affect the liver or be localized to one lobe or segment. Less than 20% of all reported cases of Caroli's disease are monolobar type. We report a case of simple type Caroli's disease confined to right lobe of the liver in a 22 year old man. He was admitted due to right upper abdominal pain and diagnosed by magnetic resonance cholangiopancreatography. He was treated with right hepatic lobectomy and recovered completely.
Adult
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Bile Ducts, Intrahepatic/pathology
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Caroli Disease/diagnosis/pathology/*surgery
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Common Bile Duct/surgery
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Diagnosis, Differential
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Hepatectomy
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Humans
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Liver/*pathology
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Magnetic Resonance Imaging
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Male
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Tomography, X-Ray Computed
5.Caroli's disease misdiagnosed as intraductal papillary neoplasm of the bile duct.
Dae Hoe GU ; Min Seon PARK ; Chang Ho JUNG ; Yang Jae YOO ; Jae Young CHO ; Yun Ho LEE ; Yeon Seok SEO ; Hyung Joon YIM ; Soon Ho UM ; Ho Sang RYU
Clinical and Molecular Hepatology 2015;21(2):175-179
Caroli's disease is a rare autosomal-recessive disorder caused by malformation of the ductal plate during embryonic development. Although it is present at birth, Caroli's disease is typically not diagnosed until between the second and fourth decades of life, as it was in the present patient. Here we report a rare case of Caroli's disease limited to one liver segment, which was initially misdiagnosed as an intraductal papillary neoplasm of the bile duct. The asymptomatic patient was treated with liver segmentectomy.
Adult
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Bile Duct Neoplasms/diagnosis/pathology
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Bile Ducts, Intrahepatic
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Caroli Disease/*diagnosis/pathology
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Diagnostic Errors
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Humans
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Magnetic Resonance Imaging
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Male
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Tomography, X-Ray Computed
6.Caroli Syndrome with Autosomal Recessive Polycystic Kidney Disease.
The Korean Journal of Gastroenterology 2011;57(1):51-53
No abstract available.
Caroli Disease/complications/*diagnosis
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Child
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Cholangiopancreatography, Magnetic Resonance
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Creatinine/blood
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Female
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Humans
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Liver/pathology
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Liver Transplantation
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Polycystic Kidney, Autosomal Recessive/complications/*diagnosis/ultrasonography
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Tomography, X-Ray Computed
7.Congenital hepatic fibrosis with Caroli's disease: report of three cases.
Ya-dong WANG ; Wen-ge SHAO ; Cai-yan ZHAO
Chinese Journal of Hepatology 2009;17(8):634-635
Adult
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Bile Ducts, Intrahepatic
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diagnostic imaging
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pathology
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Biopsy, Needle
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Caroli Disease
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complications
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diagnosis
;
pathology
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Child
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Diagnosis, Differential
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Female
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Humans
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Liver
;
diagnostic imaging
;
pathology
;
Liver Cirrhosis
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complications
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congenital
;
diagnosis
;
pathology
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Male
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Spleen
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diagnostic imaging
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pathology
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Tomography, X-Ray Computed
8.Diagnosis and differential diagnosis of intrahepatic bile duct lesions.
Chinese Journal of Pathology 2011;40(1):56-59
Adenocarcinoma
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metabolism
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pathology
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Adenoma
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pathology
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Bile Duct Neoplasms
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metabolism
;
pathology
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Bile Ducts, Intrahepatic
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CA-19-9 Antigen
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metabolism
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Cadherins
;
metabolism
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Caroli Disease
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pathology
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Cholangiocarcinoma
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pathology
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Cystadenocarcinoma
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metabolism
;
pathology
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Cystadenoma
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metabolism
;
pathology
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Cysts
;
pathology
;
Diagnosis, Differential
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Hamartoma
;
pathology
;
Humans
;
Keratin-19
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metabolism
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Keratin-20
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metabolism
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Keratin-7
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metabolism
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Liver Diseases
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pathology