Results 61 to 70 of about 31,874 (263)

Caroli Syndrome in a Child: A Case Report

Case Reports in Clinical Practice, 2019
Introduction: Caroli syndrome is a congenital disorder characterized by multiple segmental or saccular dilatations of the intrahepatic bile ducts associated with congenital hepatic fibrosis.
Pantea Tajik, Amir Hossein Goudarzian
doaj   +1 more source

Biliary complications after liver transplantation: With special reference to the biliary cast syndrome and techniques of secondary duct repair [PDF]

, 1977
In 93 consecutive cases of orthotopic liver transplantation, there were 24 examples of biliary obstruction and eight of bile fistula formation. Six of the obstructed livers developed biliary cast formation so extensive that the smaller intrahepatic ducts
Hansbrough, JF, Porter, KA, Putnam, CW, Reid, HAS, Starzl, TE   +4 more
core  

Percutaneous transhepatic cholangiography and biliary drainage after liver transplantation: A five-year experience [PDF]

, 1987
Evaluation of the biliary tract by percutaneous transhepatic cholangiography (PTC) is often required in liver transplant patients with an abnormal postoperative course.
AB Zajko, AG Tzakis, Albert B. Zajko, David H. Thiel, DH Thiel Van, DJ Gallacher, G Martineau, J Northover, JC Gartner Jr, JJ Malatack, JMA Northover, JT Ferrucci Jr, Klaus M. Bron, Rajan Behal, RY Calne, RY Calne, S Iwatsuki, TE Starzl, TE Starzl, TE Starzl, TE Starzl, TE Starzl, TE Starzl, TE Starzl, TE Starzl, Thomas E. Starzl, W Molnar, William L. Campbell   +27 more
core   +1 more source

Impact of Recanalization on Liver Hypertrophy after Portal Vein Embolization and the Role of Re‐Embolization

Annals of Gastroenterological Surgery, EarlyView.
This retrospective study of 249 patients undergoing hepatectomy after right portal vein embolization (PVE) demonstrated that major recanalization–defined as recanalization more than one segment within the embolized liver–was associated with impaired regeneration of the future liver remnant (FLR).
Masao Uemura, Shimpei Otsuka, Ryo Ashida, Katsuhisa Ohgi, Mihoko Yamada, Rui Sato, Takeshi Aramaki, Akifumi Notsu, Katsuhiko Uesaka, Teiichi Sugiura   +9 more
wiley   +1 more source

Unclassified Diffuse Ductal Cholangiocarcinoma; Report of a Case

Case Reports in Surgery, 2014
Cholangiocarcinoma (CCA) is the second most common malignant tumor of the liver. It is simply classified as intrahepatic and extrahepatic CCA (including perihilar and distal extra hepatic CCA) according to the anatomic localization.
Ünal Aydın, İsmail Özsan, Türker Karabuğa, Özcan Alpdoğan, Ragıp Ortaç, Ömer Yoldaş, Erkan Şahin   +6 more
doaj   +1 more source

Choledochal cyst with a twist: Type 1 choledochal cyst and dilated cystic duct with aberrant accessory right hepatic drainage

Journal of Pediatric Surgery Case Reports, 2023
Choledochal cysts are rare cystic dilations of the biliary tree that typically involve the extrahepatic bile duct and more infrequently, the intrahepatic bile ducts. Todani's classification of choledochal cysts is the most referenced system in which five
Pia V. Sodhi, Erin Glennon, Sarah McIntyre, Shailee Lala, Laura Martin, Sandra Tomita   +5 more
doaj   +1 more source

Intrahepatic cholangiocarcinoma: review and update [PDF]

, 2018
Cholangiocarcinoma (CCA) is a heterogeneous group of malignancies that could develop at any level from the biliary tree. CCA is currently classified into intrahepatic (iCCA), perihilar and distal on the basis of its anatomical location.
Alvaro, Domenico, Bragazzi, Maria Consiglia, Cardinale, Vincenzo, Carpino, Guido, Di Matteo, Sabina, Gaudio, Eugenio, Nevi, Lorenzo, Overi, Diletta   +7 more
core   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

A CASE OF INTRAHEPATIC BILE DUCT STONES ASSOCIATED WITH INTRAHEPATIC BILE DUCT CARCINOMA

The journal of the Japanese Practical Surgeon Society, 1990
A case of intrahepatic bile duct stones associated with intrahepatic bile duct carcinoma is reported. The case was a 68-year-old man complaining of epigastralgia which was which was developed since 1988. The patient had undergone cholecystectomy in 1955. He was diagnosed to have intrahepatic bile duct stones and admitted to this hospital for operation.
Junji TAMURA, Hiroyuki IWASE, Akio NOUMI, Masaaki SUZUKI, Noriyuki KUWABARA, Kazuhiro TAKI   +5 more
openaire   +2 more sources

Standardized Management Pathway to Prevent Acute Rejection After Liver Transplantation Following ICI Therapy for Downstaging HCC

Health Care Science, EarlyView.
Findings indicate that within a standardized clinical pathway integrating structured immunosuppression, therapeutic drug monitoring, and early complication surveillance, liver transplantation after ICI exposure can be performed safely without increased rejection risk.
Ning Wang, Zebin Zhu, Hao Zheng, Can Qi, Xiaodong Yuan, Xuefeng Li, Zhijun Xu, Jiwei Qin, Wei Wu, Jizhou Wang, Ruipeng Song, Zhiyong Guo, Lianxin Liu, Shu‐Geng Zhang, Björn Nashan   +14 more
wiley   +1 more source