Results 1 to 10 of about 4,879,457 (188)

Caroli disease associated with autosomal recessive polycystic kidney disease: CT imaging features of a case report [PDF]

Radiology Case Reports
Caroli disease (CD) is a rare congenital hepatobiliary disorder characterized by multifocal segmental dilatation of the intrahepatic bile ducts, which may involve the entire liver or only a specific region.
Mohammad Tahir Aien, MD, Hashmatullah Osmani, MD, Mohammad Iqbal Haqyar, MD   +2 more
doaj   +3 more sources

Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease. [PDF]

PLoS ONE, 2014
BackgroundMutations in PKHD1 cause autosomal recessive Caroli disease, which is a rare congenital disorder involving cystic dilatation of the intrahepatic bile ducts.
Xiwei Hao, Shiguo Liu, Qian Dong, Hong Zhang, Jing Zhao, Lin Su   +5 more
doaj   +3 more sources

Laparoscopic liver resection in Caroli disease: A single-centre case series [PDF]

Journal of Minimal Access Surgery, 2021
Background: Liver resection is the treatment of choice for patients with localised Caroli disease. While liver resection was traditionally performed as open procedure, this case series aims to evaluate the safety and efficacy of minimally invasive ...
Simon Wabitsch, Wenzel Schoening, Julia-Sophia Bellingrath, Christian Brenzing, Alexander Arnold, Uli Fehrenbach, Moritz Schmelzle, Johann Pratschke   +7 more
doaj   +2 more sources

Findings of cholangitis in a kidney transplant patient with Caroli disease on FDG PET/CT and MRI [PDF]

Radiology Case Reports, 2023
Caroli disease is a rare congenital disorder of segmental cystic dilatations of the intrahepatic biliary ducts that maintain communication with the rest of the biliary tree. Its typical clinical presentation is recurrent episodes of cholangitis.
Mustafa Natout, MD, Madiha M. Hijazi, MD, Mutaz Kassas, MD, Samir Mallat, MD, Mohamad Haidar, MD   +4 more
doaj   +2 more sources

Surgical management of Caroli disease in a low-mid income country: a single-center study and review of literature [PDF]

BMC Surgery
Introduction Caroli disease is an uncommon congenital condition characterized by non-obstructive intrahepatic bile duct dilation. When coupled with liver fibrosis or cirrhosis, it is termed Caroli syndrome.
Soukayna Bourabaa, Talha Laalou, Abderrahman Mansouri, Mohamed Hamid, Abdellatif Settaf   +4 more
doaj   +2 more sources

Clinical outcomes in Caroli disease and Caroli syndrome: a longitudinal observational cohort study [PDF]

Scientific Reports
Caroli’s disease (CD) and Caroli’s syndrome (CS) are rare congenital fibropolycystic liver disorders. While CS is known to be associated with more severe hepatic complications than isolated CD, direct longitudinal comparisons between the two entities ...
Amr Shaaban Hanafy, Eslam Kamal Fahmy, Rania Naguib, Moaz Abulfaraj, Ahmed F. Omar, Hend Naguib, Mohamed Mahmoud Abdelrahman, Hany A. Elkattawy   +7 more
doaj   +2 more sources

Localized cystic dilatation of the intrahepatic bile ducts as a distinct subtype of Caroli disease: a case report [PDF]

Journal of Medical Case Reports
Background Caroli disease encompasses multiple distinct entities. We report two cases of localized cystic dilatation of the intrahepatic bile ducts exhibiting a unique morphology.
Shoko Kato, Kenitiro Kaneko, Takuo Noda, Hiroshi Nouso, Yasuyuki Fukami, Tsuyoshi Sano   +5 more
doaj   +2 more sources

A case of pregnancy complicated by caroli disease [PDF]

BMC Pregnancy and Childbirth
This study reports a rare case of Caroli disease (CD) combined with pregnancy, and analyses and discusses the etiology, differential diagnosis, clinical treatment of CD, and its special characteristics during pregnancy; this study suggests that medical ...
Weiwei Wang, Xiaoteng Qiang, Xiufen Cai, Qing Bai   +3 more
doaj   +2 more sources

Prenatal diagnosis and molecular characterization of PKHD1 variants in two Chinese fetuses with Caroli disease/syndrome [PDF]

Frontiers in Genetics
BackgroundCaroli disease (CD) and Caroli syndrome (CS) are rare inherited disorders characterized by dilatation of intrahepatic bile ducts, caused by PKHD1 pathogenic variants.
Hui Huang, Sheng Zhao, Dan Wang, Shengbao Pan, Fang Liu, Peiwen Chen, Xinlin Chen   +6 more
doaj   +2 more sources

Recommendations for management of pregnancy complicated by Caroli disease: A case report and literature review [PDF]

iLIVER
We investigated the clinical and genetic characteristics of a 28-year-old pregnant Chinese woman with Caroli disease (CD) and systematically reviewed the published literature on pregnancy complicated by CD.
Chen Liang, Li Bai, Wei Hou, Wen-Yan Song, Yun-Xia Zhu, Su-Jun Zheng   +5 more
doaj   +2 more sources