Results 21 to 30 of about 1,160,128 (185)

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

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

Impaired nitric oxide-dependent endothelial function in young male individuals with obesity before the onset of symptoms and complications. [PDF]

Exp Physiol
Abstract Endothelial dysfunction drives obesity‐related complications. Doppler ultrasound measurement of blood flow during 1‐min passive leg movements (PLM) is a valuable non‐invasive tool for assessing endothelial function and nitric oxide (NO)‐mediated vasodilation.
Zuccarelli L, Baldassarre G, Bondesan A, Caroli D, De Micheli R, Tringali G, Favaretto T, Suraj-Prazmowska J, Kurpinska A, Majerczak J, Chlopicki S, Zoladz JA, Sartorio A, Grassi B.   +13 more
europepmc   +2 more sources

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

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

Suspected stenosis in Caroli syndrome: when cholangioscopy can be the game changer [PDF]

VideoGIE
Dario Gambaccini, MD, Giusi Desirè Sciumè, MD, Luigi Ruggiero, MD, Veronica Natali, MD, Gherardo Tapete, MD, Valeria Bolognesi, MD, Emanuele Marciano, MD   +6 more
doaj   +2 more sources

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

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   +1 more source

A rare case of caroli's syndrome

International Journal of Applied and Basic Medical Research, 2021
Caroli's syndrome is a rare autosomal recessive congenital disorder of the biliary tree characterized by intrahepatic bile duct dilation and hepatic fibrosis. Very few cases have been encountered in routine day-to-day practice. The patients usually present with features of cholangitis such as pain abdomen and jaundice.
Prasad, Satish Kumar, Mehta, Sameer Kumar, Poddar, Ankit   +2 more
openaire   +2 more sources

Unilobar tapering cirrhosis in a patient with Caroli syndrome associated with an abnormal common bile duct

The Turkish Journal of Gastroenterology, 2010
Caroli syndrome is a rare condition and is composed of congenital cystic dilatation of the biliary system and congenital hepatic fibrosis. Although many associated conditions are defined and hypothesized to occur concomitantly, due to the rarity of this ...
Yusuf BAYRAKTAR, Özgür HARMANCI, Gökhan GEDİKOĞLU, Ferhun BALKANCI, Osman Ersoy, Musa Aydınlı, Osman ABBASOĞLU   +6 more
doaj   +2 more sources

Laparoscopic Hepp Couinaud for the treatment of Caroli's disease: A case report

Ciencia y Salud, 2023
Caroli disease is a rare congenital disorder characterized by dilatation of intrahepatic bile ducts. The treatment could correspond to hepatic resection for localized disease.
Mohamad Hamaoui, Pedro Maldonado, Carolina Bravo, Luis Báez, Diego Arbaje, Annette García   +5 more
doaj   +1 more source

Caroli’s Syndrome: An Early Presentation [PDF]

Cureus, 2020
Fibropolycystic liver disorders (FLD) arise from abnormal development of the ductal plate and are classified according to the size of the affected hepatobiliary duct. Congenital hepatic fibrosis (CHF) has small duct involvement characterized by a variable degree of periportal fibrosis and hyperplasia without affecting the liver's architecture. Caroli's
Acevedo, Elsa, Laínez, Stephanie S, Cáceres Cano, Pablo Andrés, Vivar, Daniel   +3 more
openaire   +2 more sources