Results 141 to 150 of about 1,160,128 (185)

Caroli syndrome: a clinical case

Vrač skoroj pomoŝi (Emergency Doctor), 2020
This article covers a case of the rare, hereditarily caused disease, "Caroli Syndrome". The publication of this case is important because it shows that rare diseases occur, should be diagnosed and treated at all stages of patient care. It is important to know that this pathology is diagnosed and treated according to the state program — "Rare diseases".
T. Shindina, E. Aleksandrova, O. Minushkin, O. Kropova, Maksim Maksimov   +4 more
openaire   +1 more source

[Caroli syndrome].

Rontgen-Blatter; Zeitschrift fur Rontgen-Technik und medizinisch-wissenschaftliche Photographie, 1986
In 1958 Caroli described the syndrome of congenital, either segmental or involving the entire bile duct system, saccular extensions of the intrahepatic bile ducts. He differentiated between two types of this disease pattern. The first form concerns pure cystic dilatations of the intrahepatic bile ducts, whereas the second one is combined with hepatic ...
F, Numan, O, Cokyüksel, S, Camuşcu, K, Demir, M, Düren   +4 more
openaire   +1 more source

Caroli's syndrome.

Journal belge de radiologie, 1998
We report the case of a two-year-old girl presenting with recurrent episodes of fever and hepatomegaly. High resolution ultrasound (US) and computed tomography (CT) of the liver show dilated intrahepatic bile ducts with bridge formation and intraluminal protrusions. The extrahepatic bile duct is normal.
L, Breysem, G, Opdenakker, M, Smet, A, Uyttebroeck, G, Marchal, A L, Baert   +5 more
openaire   +1 more source

A Case of Caroli Syndrome

2022
Background: Caroli syndrome (CS) is a malformation of the bile ducts related to a congenital liver fibrosis. This syndrome is usually diagnosed before the age of 30 and the causes are poorly understood. Typical symptoms are fever, jaundice and pain under the right costal arch. CS affects only 1 in 100000 individuals and is more prevalent in Japan.
Vaišnoraitė, Eglė, Baliūnaitė, Agnė   +1 more
openaire   +1 more source

Caroli Disease, Caroli Syndrome, and Congenital Hepatic Fibrosis

2010
The cystic diseases of the liver are mostly autosomal recessive disorders with variable intrahepatic biliary dilatation and increased hepatic fibrosis either as part of the underlying defect or as a result of liver damage from recurrent episodes of ascending cholangitis.
Ronen Arnon, Henrietta Kotlus Rosenberg, Frederick J. Suchy   +2 more
openaire   +1 more source

[The Caroli syndrome].

Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen, 1980
Caroli's disease is characterized by congenital pseudocystic dilatation of the biliary tree. Inflammation and stone formation lead to clinical manifestation in the second decade. ERC and computed tomography are main diagnostic procedures. In cases, where the alterations are limited partial hepatectomy has been recommended.
M, Clemens, J O, Jost, G, Kautz, H, Schwering, B, Kessler, M, Galansky   +5 more
openaire   +1 more source

Caroli's Syndrome: A Rare Disorder

Journal of Medical Science & Research, 2013
A forty eight year old male presented with recurrent pain in right hypochondrium and fever with chill's and rigors but without icterus and pruritus. His liver function tests were normal. Magnetic resonance cholangiopancreatography revealed focal cystic dilatation of intrahepatic biliary radicles affecting all the segments of liver.
Priti Dave, AG Diwan, Deepak Deshmukh, Jay Patel   +3 more
openaire   +1 more source

Caroli’s Syndrome and Caroli’s Disease. Let’s check the differences.

2018
Learning objectives Background Findings and procedure details Conclusion Personal information ...
openaire   +1 more source

Caroli Syndrome

Mayo Clinic Proceedings, 2013
Jackson J, Liang, Patrick S, Kamath
openaire   +2 more sources

Caroli-Syndrom

RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, 2019
Karolin Baumgartner, Jens Kübler, Michael Bitzer, Hans Bösmüller, Marius Horger   +4 more
openaire   +1 more source