Results 11 to 20 of about 4,879,457 (188)

Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease

Radiology Case Reports, 2019
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).
Amanda Rivas, Monica Epelman, MD, Enrico Danzer, MD, N. Scott Adzick, MD, Teresa Victoria, MD, PhD   +4 more
doaj   +4 more sources

Caroli Disease (Clinical Observation) [PDF]

Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2019
The incidence of Caroli disease is estimated to be 1 case per 1 million people; as a result, there are very few available clinical observations. At the moment, the treatment of Caroli disease is limited to symptomatic therapy and the prevention of ...
I. G. Nikitin, A. A. Karabinenko, A. E. Nikitin, E. I. Dedov, D. G. Zhukova, E. D. Presnova, S. A. Korvyakov, R. H. Azimov, E. V. Reznik   +8 more
doaj   +2 more sources

Pediatric segmental Caroli disease: A case report and review of the literature

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Caroli disease is a rare congenital disorder causing nonobstructive segmental dilatation of intrahepatic bile ducts. Caroli disease can affect the liver diffusely or be confined to a single segment or lobe, although localized Caroli disease
Donna C. Koo, P. Nina Scalise, Andrea Bakker, Sara O. Vargas, Raja Shaikh, Alex G. Cuenca, Heung Bae Kim, Eliza J. Lee   +7 more
doaj   +2 more sources

Open resection of gastroduodenal artery aneurysm with fistulization into the duodenum 17 years after coil embolization in a patient with Caroli disease [PDF]

Journal of Vascular Surgery Cases and Innovative Techniques
Gastroduodenal artery aneurysm (GDAA) is a very rare vascular condition with a high risk of fatal rupture. Coil embolization is the recommended treatment for GDAA.
Shreef Said, MD, Benjamin Crews, BS, Cecilia Lee, BS, Anand Brahmandam, MD, Aditi M. Kapil, MD, Cassius Iyad Ochoa Chaar, MD, MPH, MS, FACS   +5 more
doaj   +2 more sources

Caroli disease combined with Banti syndrome in a woman: a case report [PDF]

Journal of International Medical Research
Caroli disease is a rare congenital malformation that predisposes to segmental cystic dilatation of the intrahepatic bile ducts. Banti syndrome is characterized by persistent splenomegaly due to chronic congestion, resulting in a low hematocrit and ...
Shian Yu, Hang Yuan, Yong Cao
doaj   +2 more sources

Caroli disease incidentally discovered in a 23-years old male: A case report [PDF]

Radiology Case Reports
This case report describes a 23-year-old male who was incidentally diagnosed with Caroli disease while investigating symptoms of recurrent upper quadrant pain and fever.
Luis F. Bonilla Larrama, Cesar U. Alas-Pineda, Anahi G. Pacheco, Victoria S. Díaz-Cerrato, Karla P. Molinero Leiva   +4 more
doaj   +2 more sources

Imaging diagnosis of Caroli-like disease with concurrent extrahepatic biliary obstruction in a young small-breed dog: case report [PDF]

Frontiers in Veterinary Science
Caroli-like disease is a rare congenital ductal plate malformation characterized by intrahepatic bile duct dilatation and has only rarely been reported in veterinary medicine.
Jinkyung Park, Sung-Yeon Cho, Matti Kiupel, Matti Kiupel, Kichang Lee, Hakyoung Yoon, Hakyoung Yoon   +6 more
doaj   +2 more sources

Caroli disease: an update on pathogenesis [PDF]

Chinese Medical Journal, 2021
Wen Shi, Ai-Ming Yang, Yuanyuan Ji
doaj   +2 more sources

Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report [PDF]

Heliyon
The WDR19 gene has been reported to be involved in nephronophthisis-related ciliopathies such as isolated nephronophthisis 13 (NPHP13), Sensenbrenner syndrome, Jeune syndrome, Senior-Loken syndrome, Caroli disease, retinitis pigmentosa and ...
Xianglian Tang, Sheng Yi, Zailong Qin, Shang Yi, Junjie Chen, Qi Yang, Shanshan Li, Jingsi Luo   +7 more
doaj   +2 more sources

Liver Transplantation for Caroli Disease [PDF]

International Journal of Organ Transplantation Medicine, 2012
Caroli disease is a rare congenital disorder characterized by multifocal, segmental dilatation of intrahepatic bile ducts. Patients with Caroli disease who have recurrent bouts of biliary infection, particularly those who also have complications related ...
M Zahmatkeshan, A Bahador, B Geramizade, V Emadmarvasti, SA Malekhosseini   +4 more
doaj   +1 more source