Results 1 to 10 of about 421 (130)

Carcinoid of the ampulla of Vater [PDF]

open access: yesJournal of Gastroenterology and Hepatology (Australia), 2005
Abstract  Endocrine neoplasms only rarely occur at the ampulla of Vater, comprising mostly carcinoids and malignant carcinoids, as well as few cases of poorly differentiated endocrine carcinomas (small cell carcinomas). Only 105 cases are reported in the literature, most as single case reports.
Mark, Hartel   +4 more
exaly   +3 more sources

Primary lymphoma of the ampulla of vater [PDF]

open access: yesCancer, 1994
A 57-year-old woman was investigated for obstructive jaundice with endoscopic retrograde cholangiopancreaticography that showed a tumor at the ampulla of Vater. A Whipple's procedure was performed. A protuberant tumor was present at the ampulla of Vater in the background of multiple mucosal polyps in the duodenum.
J Rode, Joya Pawade, Jürgen Rode
exaly   +3 more sources

A Case of Severe Acute Pancreatitis Following Endoscopic Biopsy of the Ampulla of Vater: A Rare Adverse Event of Esophagogastroduodenoscopy

open access: yesDEN Open
Histological biopsy is essential for diagnosing ampullary tumors; however, it can occasionally result in severe adverse events. A 49‐year‐old male underwent esophagogastroduodenoscopic screening, which revealed an ampulla of Vater with enlargement of the
Tetsushi Azami   +8 more
doaj   +2 more sources

Ampulla of Vater carcinoma: advancement in the relationships between histological subtypes, molecular features, and clinical outcomes

open access: yesFrontiers in Oncology, 2023
The incidence of ampulla of Vater carcinoma, a type of periampullary cancer, has been increasing at an annual percentage rate of 0.9%. However, patients with ampulla of Vater carcinoma have quite different prognoses due to the heterogeneities of the ...
Hao Liang, Yu Zhu, Ya-kun Wu
doaj   +1 more source

Mixed neuroendocrine–non-neuroendocrine neoplasm of the ampulla of Vater: a case report

open access: yesSurgical Case Reports, 2023
Background Mixed neuroendocrine–non-neuroendocrine neoplasms of the ampulla of Vater are rare and heterogenous, making it difficult to achieve a definitive preoperative diagnosis.
Kenjiro Date   +8 more
doaj   +1 more source

Uterine cervix squamous cell carcinoma metastatic to the Ampulla of Vater: a case report with review of the literature

open access: yesJournal of Health Sciences, 2013
Metastases to gastrointestinal tract are uncommon. In particular, metastases to the ampulla of Vater are very rare and may represent a significant diagnostic challenge.
Dalma Udovčić Gagula   +6 more
doaj   +3 more sources

Carcinoma of the Ampulla of Vater

open access: yesAnnals of Surgery, 1987
Thirty-five consecutive cases of adenocarcinoma of the ampulla of Vater seen over the past 36 years were reviewed. The introduction of new diagnostic techniques over the course of this study improved the accuracy of preoperative diagnosis but did not lead to earlier diagnosis.
Hayes, Daniel H.   +3 more
openaire   +7 more sources

Acute Pancreatitis Following Endoscopic Ampullary Biopsies without Attempted Cannulation of the Ampulla of Vater [PDF]

open access: yesClinical Endoscopy, 2016
A 51-year-old man underwent diagnostic work-up for an abnormal-appearing ampulla of Vater. Three hours after biopsy of the ampulla, the patient presented with intense symptoms suggesting acute pancreatitis, which was later confirmed with laboratory and ...
Spyridon Michopoulos   +5 more
doaj   +1 more source

Metastatic rectal cancer in the ampulla of Vater: A unique case

open access: yesCancer Reports, 2022
Background A metastatic lesion located in the ampulla of Vater is considered extremely rare, with only 32 cases reported globally. Case A 65‐year‐old patient was primarily diagnosed with a rectal adenocarcinoma.
Athina A. Samara   +8 more
doaj   +1 more source

Post-Metachronous Cancer of the Ampulla of Vater after Gastric Cancer Surgery: An Overview

open access: yesJournal of the Dow University of Health Sciences, 2022
Post-metachronous ampulla of Vater carcinoma after gastric cancer is an extremely rare between multiple primary cancers. The published literature contains only a few cases. Among the cases males are found more frequently.
Mehmet Yildirim   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy