Results 31 to 40 of about 4,240 (196)

Zollinger-Ellison syndrome: a case report

open access: yesZdravniški Vestnik, 2006
Background: Zollinger-Ellison syndrome is the consequence of excessive and autonomous secretion of gastrin from gastrinoma cells. The disease is exceptionally rare and characterized by severe and treatment-resistant peptic disease that can become life ...
Mitja Krajnc, Miro Čokolič
doaj   +2 more sources

Case report: optimal tumor cytoreduction and octreotide with durable disease control in a patient with MEN-1 and Zollinger-Ellison syndrome—over a decade of follow-up [PDF]

open access: yesWorld Journal of Surgical Oncology, 2019
Background Zollinger-Ellison syndrome (ZES) is a rare condition characterized by hypersecretion of gastrin by gastrinoma tumors leading to severe peptic ulcer disease with potential development of gastric carcinoid tumors.
Lynsey M. Daniels   +6 more
doaj   +2 more sources

Zollinger–Ellison syndrome: modern aspects of diagnostics and treatment

open access: yesРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии, 2014
The aim of review. To reflect modern concepts on clinic, diagnostics and treatment of Zollinger–Ellison syndrome (ZES).Key points. ZES is rare disease related to intragastric hyperacidity.
I. V. Mayev   +3 more
doaj   +2 more sources

A Perplexing Case of Abdominal Pain That Led to the Diagnosis of Zollinger-Ellison Syndrome [PDF]

open access: yesCase Reports in Gastrointestinal Medicine, 2017
Zollinger-Ellison syndrome (ZES) is a rare clinical disorder, characterized by hypersecretion of gastric acid and multiple ulcers distal to the duodenal bulb. This occurs via the release of gastrin by neuroendocrine tumors known as gastrinomas.
Adrienne Lenhart   +4 more
doaj   +2 more sources

Diagnosis of Zollinger-Ellison syndrome in the era of PPIs, faulty gastrin assays, sensitive imaging and limited access to acid secretory testing. [PDF]

open access: yesInt J Endocr Oncol, 2017
In recent years, the diagnosis of Zollinger–Ellison syndrome has become increasingly controversial with several new approaches and criteria proposed, differing from the classical biochemical criterion of inappropriate hypergastrinemia (i.e ...
Metz DC   +4 more
europepmc   +2 more sources

Surgical Management of Zollinger-Ellison Syndrome in Multiple Endocrine Neoplasia Type 1 an AFCE and GTE Cohort Study. (Association Francophone de Chirurgie Endocrinienne and Groupe d'étude des Tumeurs Endocrines). [PDF]

open access: yesWorld J Surg
To describe surgical indications, procedures and outcomes in patients operated for Zollinger‐Ellison syndrome (ZES) in multiple endocrine neoplasia type 1 (MEN1) using a large nationwide cohort. ABSTRACT Objective To describe surgical indications, procedures and outcomes in patients operated for Zollinger‐Ellison syndrome (ZES) in multiple endocrine ...
Gaujoux S   +27 more
europepmc   +2 more sources

An Update on Zollinger-Ellison Syndrome [PDF]

open access: yes, 2023
: Zollinger-Ellison syndrome is a rare disease, characterized by the presence of acid hypersecretion, gastric-duodenal ulcer disease, and a gastrin-secreting pancreatic or extrapancreatic tumor with difficult primary location.
Boddula Mahathi   +1 more
core   +1 more source

The Zollinger–Ellison Syndrome

open access: yesNew England Journal of Medicine, 2022
A 75-year-old man presented to the emergency department with a 6-month history of epigastric pain, watery diarrhea, and weight loss. Physical examination was notable for epigastric tenderness. Esophagogastroduodenoscopy revealed severe esophagitis (Panel A), antral erosions, and duodenal ulcers (Panel B). [...]
Quentin Binet, Ivan Borbath
openaire   +3 more sources

Conjunctival myxoid stromal tumor of the palpebral conjunctiva: A case report

open access: yesAmerican Journal of Ophthalmology Case Reports, 2022
Purpose: To present the importance of considering conjunctival myxoid stromal tumors in the differential when evaluating eyelid lesions as these tumors could indicate undetected systemic syndromes including Zollinger-Ellison Syndrome, Carney complex, and
Pamela S. Martin   +3 more
doaj   +1 more source

Synchronous Peripancreatic Lymph Node Gastrinoma and Gastric Neuroendocrine Tumor Type 2 [PDF]

open access: yesClinical Endoscopy, 2016
A 34-year-old man was referred to our hospital with gastric polypoid lesions and biopsy-confirmed neuroendocrine tumor (NET). Computed tomography (CT) revealed a 3×3.5×8-cm retroperitoneal mass behind the pancreas, with multiple hepatic metastases.
Hee Woo Lee   +7 more
doaj   +1 more source

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