Results 121 to 130 of about 444,549 (313)

Choledochal Cyst in the Adult

Annals of Surgery, 1995
The authors examined the natural history of choledochal cysts in adults treated surgically.An initial diagnosis of choledochal cyst is uncommon in adults. The recommended treatment is excision, rather than bypass, to achieve effective biliary drainage and because of the risk of cancer.A retrospective study of 27 adult patients was completed to ...
Carol R. Guthrie, Arthur J. Donovan, Steven C. Stain, Albert E. Yellin   +3 more
openaire   +4 more sources

Laparoscopic Excision Versus Open Excision for the Treatment of Choledochal Cysts: A Systematic Review and Meta-Analysis

International surgery, 2015
In 1723, Vater first described choledochal cyst and in 1977, Todani et al classified this disease. For many years, open excision (OP) as the standard procedure made a great impact in the treatment of choledochal cyst. Since 1995, when Farello et al first
Chen Zhen, Z. Xia, L. Long, Ma Lishuang, Yu Pu, Wenjuan Zheng, Xiaofan Li   +6 more
semanticscholar   +1 more source

Upper gastrointestinal endoscopy in the surgically altered patient

Digestive Endoscopy, Volume 36, Issue 10, Page 1077-1093, October 2024.
As management of upper gastrointestinal malignancies improves, and with popularization of bariatric surgery, endoscopists are likely to meet patients with altered upper gastrointestinal anatomy. Short‐term, the surgery can cause complications like bleeding, leaks, and fistulas, and longer‐term problems such as intestinal or biliary anastomotic ...
Purnima Bhat, Arthur John Kaffes, Kristoffer Lassen, Lars Aabakken   +3 more
wiley   +1 more source

Management of intrahepatic and perihilar cholangiocarcinomas: Guidelines of the French Association for the Study of the Liver (AFEF)

Liver International, Volume 44, Issue 10, Page 2517-2537, October 2024.
Abstract Intrahepatic cholangiocarcinoma (iCCA) is the second most common malignant primary liver cancer. iCCA may develop on an underlying chronic liver disease and its incidence is growing in relation with the epidemics of obesity and metabolic diseases.
Cindy Neuzillet, Marie Decraecker, Hélène Larrue, Line C. Ntanda‐Nwandji, Louise Barbier, Sandrine Barge, Arthur Belle, Carine Chagneau, Julien Edeline, Catherine Guettier, Florence Huguet, Jérémie Jacques, Brigitte Le Bail, Sarah Leblanc, Maïté Lewin, David Malka, Maxime Ronot, Véronique Vendrely, Éric Vibert, Christophe Bureau, Marc Bourliere, Nathalie Ganne‐Carrie, Jean‐Frédéric Blanc   +22 more
wiley   +1 more source

Choledochal cyst of the cystic duct: Report of imaging findings in three cases and review of literature

Indian Journal of Radiology and Imaging, 2015
The choledochal cysts, which refer to the cystic dilatation of the biliary duct, are rare lesions generally seen in children. Choledochal cyst of the cystic duct is an uncommon entity.
Sonali Sethi, Lalendra Upreti, Amit K Verma, Sunil K Puri   +3 more
doaj   +1 more source

Congenital biliary anomaly with secondary cholangiohepatitis in a Siamese cross kitten [PDF]

, 2016
A 5-month-old Siamese cross kitten was presented with jaundice and a palpable abdominal mass at the right cranial quadrant. The extra-hepatic biliary system was markedly distended upon abdominal ultrasonography.
Khor, Kuan Hua, Leong, Zi Ping, Mohamed Mustapha, Noordin, Rahman, N., Watanabe, Malaika, Yiew, Xiu Ting   +5 more
core  

Integrative analysis reveals different feature of intrahepatic cholangiocarcinoma subtypes

Liver International, Volume 44, Issue 9, Page 2477-2493, September 2024.
Abstract Background & Aims Intrahepatic cholangiocarcinoma (iCCA) has two main histological subtypes: large and small duct‐type iCCA, which are characterized by different clinicopathological features. This study was conducted with the purpose of expanding our understanding of their differences in molecular features and immune microenvironment.
Zhuomiaoyu Chen, Jie Gao, Zuyin Li, Delin Ma, Yang Wang, Qian Cheng, Jiye Zhu, Zhao Li   +7 more
wiley   +1 more source

Choledochal cyst type I in infant: a case report [PDF]

Romanian Journal of Pediatrics
Choledochal cysts are rare congenital anomalies characterized by dilatation of the bile ducts. The most frequent subtype of choledochal cyst is type I, which has fusiform dilatation of the common bile duct and poses significant challenges in diagnosis ...
Steven Christian Susianto, Rendi Aji Prihaningtyas, Bagus Setyoboedi, Sarwendah Pratiwi Budiman, Fendy Matulatan, Sjamsul Arief   +5 more
doaj   +1 more source

Caso Raro de Quisto do Colédoco Todani Tipo III [PDF]

, 2020
rare biliary tree disorders, which are divided in several subtypes according to Todani classification. Type III choledochal cyst is one of the rarest subtype.
Gil, P, Lourenço, AL, Proença Caetano, A   +2 more
core  

Surgical Treatment of Coledochal Cyst Associated with an Aberrant Posterior Hepatic Duct: Report of a Case and Brief Literature Review [PDF]

, 2011
Choledochal cysts (CCs) are rare congenital cystic or fusiform dilatations of the biliary tree that can involve the extrahepatic and/or intrahepatic biliary tree. We report a case of huge type I CC associated with an aberrant posterior hepatic duct. A 52-
Antonio Sciuto, Carmelo Sciumè, Chiara Lo Nigro, Enrico Arnone, Frampas E, Girolamo Geraci, Giuseppe Modica, Matos C, Rush E   +8 more
core   +3 more sources