Results 51 to 60 of about 2,487 (162)
JGH Open, Volume 9, Issue 9, September 2025.ABSTRACT Gastric neuroendocrine neoplasms are a rare type of stomach cancer, classified into well‐differentiated neuroendocrine tumors (NETs) and poorly differentiated neuroendocrine carcinomas (NECs). Gastric NETs (G‐NETs) originate from endocrine progenitor cells in the basal layer of the mucosa, primarily in the setting of chronic atrophic gastritis,
Katsunori Matsueda +4 more
wiley +1 more source
De novo Gastrinoma: A Case Report
GE: Portuguese Journal of Gastroenterology, 2019 Gastrinomas are neuroendocrine tumors characterized by gastrin overexpression – 80% are sporadic and 20% are associated with multiple endocrine neoplasia type 1.
Arsénio Barbosa +4 more
doaj +1 more source
Cholecystokinin: Clinical aspects of the new biology
Journal of Internal Medicine, Volume 298, Issue 3, Page 251-267, September 2025.Abstract Cholecystokinin (CCK) is a classic gut hormone that has been known for almost a century to regulate gallbladder emptying, pancreatic enzyme secretion, and gastrointestinal motor activity. In 1968, the CCK structure was identified by Viktor Mutt and Erik Jorpes from porcine gut extracts as a peptide of 33 amino acid residues.
Jens F. Rehfeld
wiley +1 more source
Zollinger-Ellison Syndrome: A Narrative Review of Clinical Presentation, Pathogenesis, Diagnosis and Modern Management Approaches [PDF]
Journal of Clinical and Diagnostic ResearchZollinger-Ellison Syndrome (ZES) is rare disorder which is caused by gastrin-secreting neuroendocrine tumours known as gastrinomas, primarily located in the duodenum or pancreas.
Jaideep Reddy +4 more
doaj +1 more source
Digestive Endoscopy, Volume 37, Issue 8, Page 834-843, August 2025.Objectives Lymph node metastasis (LNM) is crucial in determining treatment strategies for gastric neuroendocrine tumors (gNETs). While type 3 is considered more aggressive than types 1 and 2 within the clinical subtype of gNETs, the supporting data were insufficient, due to their rarity. We aimed to study the prevalence and risk factors associated with
Yohei Ogata +9 more
wiley +1 more source
Evolution of clinical ideas about Zollinger-Ellison syndrome
Терапевтический архив, 2014 The paper gives the current views of the diagnosis and treatment of Zollinger-Ellison syndrome (ZES). It underlines the importance of including ZES in differential diagnosis in patient with frequently recurrent and standard-dose proton pump inhibitor ...
I V Maev +3 more
doaj
Sporadic duodenal macrogastrinoma: a rare case report
Acta Medica Lituanica, 2013 Gastrinomas are rare neuroendocrine tumors characterized by the secretion of gastrin, which causes hyperchlorhydria, thereby producing the Zollinger-Ellison syndrome. In most cases this syndrome manifests as severe peptic ulcer disease. We are presenting
Dainius Šimčikas +5 more
doaj +1 more source
Zollinger–Ellison syndrome: modern aspects of diagnostics and treatment
Российский 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
Zollinger–Ellison syndrome in a 12-year-old child
Journal of Indian Association of Pediatric Surgeons, 2017 The syndrome described by Zollinger and Ellison in 1955 is a rare clinical entity which is even rarer in children. This report describes a 12-year-old boy who presented with refractory peptic ulcer disease which was finally diagnosed to be due to a ...
Abir Lal Nath +5 more
doaj +1 more source