Results 31 to 40 of about 81,268 (224)

A case of hepatic intraductal papillary neoplasm of the bile duct

open access: yesArchives of Case Reports, 2023
Introduction: Intraductal Papillary Neoplasm of the Bile ducts (IPNB) is a rare entity characterized by exophytic growth of the bile ducts. Case presentation: In this report, we present a 57-year-old male with no prior medical history consulted for upper
Beltaifa Dorsaf   +6 more
semanticscholar   +1 more source

postulating a common tumor entity [PDF]

open access: yes, 2016
The set definition of distal cholangiocarcinomas and adenocarcinomas of the pancreatic head is challenged by their close anatomical relation, similar growth pattern, and corresponding therapeutic outcome. They show a mutual development during embryologic
Bahra, Marcus   +4 more
core   +1 more source

Invaginated ampulla of Vater in synchronous malignant intraductal papillary mucinous neoplasm of the pancreas and common bile duct cancer [PDF]

open access: yesEndoscopy, 2013
A 61-year-old woman was admitted for upper abdominal pain and fever. Laboratory findings showed raised neutrophil ratio and amylase and lipase levels. Abdominal computed tomography (CT) scan revealed diffuse swelling of the pancreas with peripancreatic fluid, and mild dilatation of the mid-pancreatic duct. Endoscopic retrograde cholangiopancreatography
J W, Han   +4 more
openaire   +3 more sources

Total Pancreatectomy for Ampullary Adenocarcinoma in a 74-Year-Old Patient: Case Report and Literature Review

open access: yesCase Reports in Surgery, 2020
Primary ampullary neoplasms have origin in the ampulla of Vater, an anatomical structure where the common bile duct and the pancreatic duct join together as a common channel. It represents
Gabriela A. Arroyo Murillo   +3 more
doaj   +1 more source

Genetic Tracing of Clonal Expansion and Progression of Pancreatic Ductal Adenocarcinoma: A Case Report and Multi-Region Sequencing Analysis

open access: yesFrontiers in Oncology, 2020
Pancreatobiliary tumors frequently contain multiple malignant and precancerous lesions; however, the origin of the driver mutations and the mechanisms that underlie the generation of distinct clones within an organ field remain unclear.
Shion Tachibana   +24 more
doaj   +1 more source

Role of Ayurveda in symptomatic management of pancreatic neuro endocrine tumor - An experience

open access: yesJournal of Ayurveda Case Reports, 2022
The incidental diagnosis of neoplasms has greatly increased due to the widespread use of advanced imaging techniques. Pancreatic neuroendocrinal tumors (pNET) comprise 7% of the neuroendocrine tumors (NETs) that can be functional or nonfunctional ...
Sunil Kumar   +4 more
doaj   +1 more source

Liver Resection for Primary Hepatic Neoplasms. [PDF]

open access: yes, 1988
Subtotal hepatic resection was performed in 356 patients; 87 had primary hepatic malignancies, 108 had metastatic tumors, and 161 had benign lesions including 8 traumatic injuries. The global mortality was 4.2%.
C. Couinaud   +16 more
core   +1 more source

Istoadenoma do ducto biliar comum

open access: yesRevista 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   +2 more
doaj   +1 more source

Two cases of cholangiocarcinoma in diabetes mellitus causing worsening of glycemic control and acute liver dysfunction

open access: yesJournal of Clinical and Translational Endocrinology Case Reports, 2018
This is a report of 2 cases of sudden and simultaneous worsening of glycemic control and acute liver dysfunction (biliary obstruction) suggestive of extrahepatic cholangiocarcinoma (ECC). Case 1 was a 59-year-old woman with a history of diabetes mellitus,
Masaru Oota
doaj   +1 more source

Liver Transplantation for Alagille's Syndrome [PDF]

open access: yes, 1993
Twenty-three children with Alagille's syndrome and end-stage liver disease underwent liver transplantation with cyclosporine and low-dose steroid immunosuppression. Two to 9 years (mean, 4.4 years) after surgery, 13 (57%) of the children were still alive,
Reyes, J   +5 more
core   +1 more source

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