scholarly journals Congenital Dilatation of the Bile Ducts (Caroli's Disease) in Young Dogs

2003 ◽  
Vol 17 (1) ◽  
pp. 28-32 ◽  
Author(s):  
S. Görlinger ◽  
J. Rothuizen ◽  
S. Bunch ◽  
T.S.G.A.M. Ingh
1992 ◽  
Vol 28 (1) ◽  
pp. 124 ◽  
Author(s):  
Moon Gyu Lee ◽  
Boo Kyung Han ◽  
Seong Yon Baek ◽  
Kyoung Sik Cho ◽  
Yong Ho Auh ◽  
...  

2020 ◽  
Vol 31 (2) ◽  
pp. 107-110
Author(s):  
Lemfadli Y ◽  
Bouchrit S ◽  
Ait Errami A ◽  
Oubaha S ◽  
Samlani Z ◽  
...  

This article describes a case of Caroli’s disease in a 53-year-old female patient who complained nonspecificabdominal pain without cholestasis or cholangitis. Ultrasound and hepatic magnetic resonanceimaging showed segmental saccular dilations connected to intrahepatic bile ducts without hepaticfibrosis. This clinical case shows the possibility of having oligosymptomatic forms in the diffuse formsof Caroli disease, therefore the interest to consider this diagnosis in case of non-specific abdominalsigns and to request a hepatic ultrasound. Bangladesh J Medicine July 2020; 31(2) : 107-110


Author(s):  
S. Görlinger ◽  
J. Rothuizen ◽  
S. Bunch ◽  
T.S.G.A.M. van den Ingh

Radiology ◽  
1978 ◽  
Vol 127 (3) ◽  
pp. 746-746 ◽  
Author(s):  
Javier Lucaya ◽  
Jose Luis Gomez ◽  
Ceferino Molino ◽  
Juan Gonzalez Atienza

2021 ◽  
Vol 13 (3) ◽  
pp. 150-152
Author(s):  
G. G. Kuttykuzhanova ◽  
A. Zh. Tanirbergenova ◽  
S. Zh. Abdirazakova ◽  
Z. Zh. Urikbaeva

In their medical practice doctors deal with rare diseases which present difficulties in making a clinical diagnosis, in this case additional diagnostic methods are required. One of these diseases is Caroli's disease (syndrome), characterized by cystic enlargement of the intrahepatic bile ducts with frequent formation of intrahepatic stones. Taking into account the difficulties of early diagnosis, we present our own observation.


Author(s):  
R.D. Last ◽  
J.M. Hill ◽  
M. Roach ◽  
T. Kaldenberg

Two, sibling, male Golden retriever puppies, 13 weeks of age, were presented with congenital biliary cysts of the liver involving both hepatic and segmental bile ducts, as well as bilateral polycystic kidney disease. Ultrasonography of the livers of both pups demonstrated segmental cystic lesions that were contiguous with the bile ducts. Histopathology revealed cystic ectatic bile duct hyperplasia and dysplasia with variable portal fibrosis in the liver, while in the kidneys there were radially arranged, cylindrically dilated cysts of the collecting ducts, which extended through the medulla and cortex. This pathology was compatible with that of congenital dilatation of the large and segmental bile ducts (Caroli's disease) described in humans, dogs and rats. In humans Caroli's disease has an autosomal recessive inheritance pattern, while in rats activation of the MEK5/ERK cascade initiates the biliary dysgenesis of Caroli's disease in this species. However, the exact mode of inheritance and pathogenesis of Caroli's disease in dogs is as yet unknown. Previous reports on congenital hepatic cystic diseases of the dog have described Caroli's disease like lesions in various breeds, but these are believed to be the 1st reported cases in the Golden retriever breed.


2017 ◽  
pp. 85-89
Author(s):  
T. N. Galyan ◽  
N. S. Tarba ◽  
V. V. Khovrin ◽  
L. O. Polizhuk ◽  
N. N. Bagmet ◽  
...  

Caroli’s disease is a rare inherited disorder characterized by nonobstructive saccular or fusiform dilation of the intrahepatic bile ducts. Two main types of Caroli’s disease are reported, the true type with isolated dilation of intrahepatic bile ducts of single liver segment with formation of stones and development of cholangitis. The second type is combined with a congenital hepatic fibrosis. The true type of Caroli’s disease is distinct from primary sclerosing cholangitis, polycystic disease, cholangiolithiasis and other diseases. This paper presents a literature review and a case of monolobar Caroli’s disease with intrahepatic stones. The difficulties of preoperative differential diagnosis are shown. 


2009 ◽  
Vol 217 (3) ◽  
pp. 442-451 ◽  
Author(s):  
Mitsue Yasoshima ◽  
Yasunori Sato ◽  
Shinichi Furubo ◽  
Kazuo Kizawa ◽  
Takahiro Sanzen ◽  
...  

1989 ◽  
Vol 30 (5) ◽  
pp. 459-462 ◽  
Author(s):  
M. Höglund ◽  
C. Muren ◽  
D. Schmidt

Caroli's disease is a rare congenital disease with multiple segmental dilatations of the bile ducts. It may present in two forms: one (the simple form) with segmental dilatations only, and the other with dilatations combined with fibroangioadenomatosis, frequently complicated by portal hypertension. The disease is thought to be recessively inherited, but few familial cases have been reported. We have observed two sisters with the disease, one with the simple form, the other with fibroangioadenomatosis. Their case histories and diagnostic findings, with special reference to ultrasonography and computed tomography, are presented, and the potential for diagnosis by different imaging modalities is discussed.


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