Results 51 to 60 of about 28,264 (256)

Istoadenoma do ducto biliar comum

Revista do Colégio Brasileiro de Cirurgiões
Biliary duct cystoadenomas are rare neoplasms, with about 120 cases described in the literature, including cystoadenomas and cystoadenocarcinomas. The authors report a case of cystoadenoma of the common bile duct in a 45-year-old woman with history of ...
José de Souza Andrade Filho, Gil Patrus Mundim Pena, Domingos André F. Drummond   +2 more
doaj   +1 more source

Intraductal papillary mucinous neoplasm of the biliary tract in the caudate lobe of the liver: a case report and literature review

Frontiers in Oncology, 2023
An intraductal papillary mucinous neoplasm of the biliary tract (BT-IPMN) in the caudate lobe of the liver is a rare tumor originating from the bile duct.
Xunhao Zhu, Qingqiang Ni, Qianchang Wang, Chaoqun Ma, Faji Yang, Hengjun Gao, Huaqiang Zhu, Xu Zhou, Hong Chang, Jun Lu, Fangfeng Liu   +10 more
doaj   +1 more source

Vanishing bile duct syndrome related to DILI and Hodgkin lymphoma overlap: A rare and severe case

Annals of Hepatology, 2020
Vanishing bile duct syndrome is a rare acquired condition, characterized by progressive loss of intrahepatic bile ducts leading to ductopenia and cholestasis.
Raquel D. Greca, Marlone Cunha-Silva, Larissa B.E. Costa, Júlia G.F. Costa, Daniel F.C. Mazo, Tiago Sevá-Pereira, Marlla M.C. Nascimento, Isadora E. Pereira, Flávia C. Oliveira, Guilherme A.S. Faria, Fernando L.P. Neto, Jazon R.S. Almeida   +11 more
doaj  

Caroli's disease misdiagnosed as intraductal papillary neoplasm of the bile duct [PDF]

Clinical and Molecular Hepatology, 2015
Caroli's disease is a rare autosomal-recessive disorder caused by malformation of the ductal plate during embryonic development. Although it is present at birth, Caroli's disease is typically not diagnosed until between the second and fourth decades of life, as it was in the present patient. Here we report a rare case of Caroli's disease limited to one
Ho Sang Ryu, Jae Young Cho, Yun Ho Lee, Dae Hoe Gu, Soon Ho Um, Yang Jae Yoo, Hyung Joon Yim, Yeon Seok Seo, Min Seon Park, Chang Ho Jung   +9 more
openaire   +4 more sources

Resectable Cholangiocarcinoma: Reviewing the Role of Adjuvant Strategies

Clinical Medicine Insights: Oncology, 2016
Cholangiocarcinoma is a very heterogeneous and rare group of neoplasms originating from the perihilar, intra-, or extrahepatic bile duct epithelium.
E. Una Cidon
doaj   +1 more source

Large Cell Neuroendocrine Carcinoma of the Extrahepatic Bile Duct

The Korean Journal of Gastroenterology, 2018
Primary neuroendocrine tumors originating from the extrahepatic bile duct are rare. Among these tumors, large cell neuroendocrine carcinomas (NECs) are extremely rare.
Ji Young Park, Tae Joo Jeon
doaj   +1 more source

A Case of Intraductal Papillary Neoplasm of the Bile Duct with Stromal Invasion [PDF]

Case Reports in Gastroenterology, 2008
Intraductal papillary neoplasm of the bile duct (IPNB) represents biliary papillary tumors mainly growing and is considered to be of relatively low-grade malignancy. Here we report a case of IPNB in whom the poorly differentiated component deeply infiltrated the bile duct wall. A 77-year-old male had an invasive carcinoma of the bile duct 3 cm in size.
Kouichi Tomoshige, Tomayoshi Hayashi, Kenichirou Shibata, Terumitsu Sawai, Takeshi Nagayasu, Naoe Kinoshita, Yorihisa Sumida, Yasuni Nakanuma, Hiroaki Takeshita, Toru Yasutake, Atsushi Nanashima   +10 more
openaire   +3 more sources

Biliary cystadenoma and choledochal polyp: a rare association [PDF]

Journal of Clinical and Scientific Research, 2013
Biliary cystadenomas are rare, potentially malignant neoplasms of biliary origin occurring predominantly in middle aged women. Here we report a case of biliary cystadenoma in a young female who presented with an epigastric mass and features of ...
A.Y. Lakshmi, B.Vijayalakshmi Devi, P. Sriram, M. Kumaraswamy Reddy   +3 more
doaj  

A case report of vanishing bile duct syndrome after exposure to pexidartinib (PLX3397) and paclitaxel. [PDF]

, 2019
Pexidartinib (PLX3397) is a small molecule tyrosine kinase and colony-stimulating factor-1 inhibitor with FDA breakthrough therapy designation for tenosynovial giant-cell tumor, and currently under study in several other tumor types, including breast ...
Chien, A Jo, Esserman, Laura J, Hyland, Colby, Piawah, Sorbarikor, Rugo, Hope S, Umetsu, Sarah E   +5 more
core  

Long-Term Risks of Benign and Malign Complications after Endoscopic Sphincterotomy in the Management of Benign Biliopancreatic Pathology: A Cohort Study

Eurasian Journal of Medicine
Background: Endoscopic retrograde cholangiopancreatography (ERCP) is the preferred technique for treating pathologies of the bile duct. It has been suggested that this procedure, combined with sphincterotomy, may influence the subsequent development of ...
Mercedes Ibáñez, Cristina López, Jeancarlos Trujillo , Juan Ramón Gómez , Carlos Vaquero Puerta, Juan Carlos Martin del Olmo   +5 more
doaj   +1 more source