Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Caroli′s syndrome"'
Autor:
Tianmin Zhou, Keyu Liu, Hao Wei, Qingmei Zhong, Daya Luo, Wenjuan Yang, Ping Zhang, Yingqun Xiao
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Caroli’s syndrome is a congenital disease characterized by dilation of intrahepatic bile ducts and congenital hepatic fibrosis. It is a rare condition in clinical work. Typically, the diagnosis of this disease is confirmed through medical
Externí odkaz:
https://doaj.org/article/bfaa7a23fe5746a197139df3806eb989
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-4 (2023)
Abstract Background Caroli’s disease is characterized by non-obstructive dilatation of intrahepatic biliary radicals with formation of calculi followed by recurrent episodes of cholangitis. It is a rare congenital malformation and often remains sil
Externí odkaz:
https://doaj.org/article/f4e651916a9f400ab94d555fc020b141
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3133-3137 (2020)
Abstract Portal hypertension is not a classical presentation of Caroli's syndrome. However, some young children can present with overt signs and symptoms indicative of advanced disease state despite the improvement in imaging technology which has dec
Externí odkaz:
https://doaj.org/article/e9ede1b5133d42629b367e30289ab595
Publikováno v:
Balkan Journal of Medical Genetics, Vol 21, Iss 2, Pp 49-53 (2018)
We report the case of a 41-year-old man on conservative treatment for more than 20 years for chronic renal insufficiency, chronic hepatitis and recurrent cholangitis. Following lengthy and extensive diagnostics, the differential diagnosis included pr
Externí odkaz:
https://doaj.org/article/c737a6688e274114942f74ccf6ebe2c8
Publikováno v:
Diagnostic Pathology, Vol 12, Iss 1, Pp 1-6 (2017)
Abstract Background Abernethy malformation is a rare congenital anomaly characterised by the partial or complete absence of the portal vein and the subsequent development of an extrahepatic portosystemic shunt. Caroli’s disease is a rare congenital
Externí odkaz:
https://doaj.org/article/8e1d6d55cbb0466b925e3a1ef394555f
Autor:
Fornari, Fernando, P. Breyer, Helenice, L. Waechter, Fábio, T. Cerski, Carlos, F. Francisconi, Carlos, Magüilnik, Ismael, R. Alvares-da-Silva, Mário, M. Pereira-Lima, Luis, R. da Silveira, Themis, G.S. Barros, Sérgio
Publikováno v:
Clinical & Biomedical Research; Vol. 18 No. 3 (1998): Periodical HCPA
Clinical and Biomedical Research; v. 18 n. 3 (1998): Revista HCPA
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Clinical and Biomedical Research; v. 18 n. 3 (1998): Revista HCPA
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Caroli’s syndrome is an uncommon disease, and it is characterized by the presenceof cystic dilation of the intrahepatic biliary tree, and of congenital fibrosis. It may act asa premalignant condition, and in some cases it may develop into cholangio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1b2f035846efc96ad75b9d1fbd90051c
https://seer.ufrgs.br/index.php/hcpa/article/view/125025
https://seer.ufrgs.br/index.php/hcpa/article/view/125025
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 12, Pp 3133-3137 (2020)
Clinical Case Reports, Vol 8, Iss 12, Pp 3133-3137 (2020)
Portal hypertension is not a classical presentation of Caroli's syndrome. However, some young children can present with overt signs and symptoms indicative of advanced disease state despite the improvement in imaging technology which has decreased it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5574d71527c41c63ec5004eafaffe22b
https://doi.org/10.1002/ccr3.3374
https://doi.org/10.1002/ccr3.3374
Publikováno v:
International Journal of Applied and Basic Medical Research
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 p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b662e973a9378cb4c02e34988c7eecce
http://europepmc.org/articles/PMC8360226
http://europepmc.org/articles/PMC8360226
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.