Results 1 to 10 of about 2,418 (113)

Canine Gastrinoma with Long-Term Survival After Primary and Repeat Surgeries Using Serial Serum Gastrin Concentrations as an Adjunctive Monitoring Marker: A Report of Two Cases [PDF]

open access: yesVeterinary Sciences
Gastrinoma is a rare neuroendocrine tumor in dogs that arises from functional pancreatic non-β cells and secretes excessive gastrin. Gastrinoma in dogs has a high metastasis rate at diagnosis, and curative treatment is often difficult.
Kyosuke Takeuchi   +5 more
doaj   +2 more sources

Primary gastrinoma of the gallbladder: a case report and review of the literature [PDF]

open access: yesFrontiers in Oncology, 2023
BackgroundPrimary gallbladder gastrinoma is an exceptionally uncommon tumor and is a rare form of neuroendocrine neoplasm. Until now, no cases of primary gallbladder gastrinoma and rare cases of primary gastrinoma from the biliary system have been ...
Yao-Ge Liu   +7 more
doaj   +2 more sources

Current Medical Controversies in Zollinger–Ellison Syndrome [PDF]

open access: yesBiomedicines
Purpose: Zollinger–Ellison syndrome (ZES) is the most frequent, functional, malignant pancreatic neuroendocrine tumor syndrome (pNET), which is due to ectopic secretion of gastrin by a pNET/NET (i.e., gastrinomas) resulting in severe, refractory acid ...
Robert T. Jensen   +2 more
doaj   +2 more sources

Esophageal Perforation in Zollinger–Ellison Syndrome: A Scoping Review of Management and Outcomes [PDF]

open access: yesJGH Open
Esophageal perforation in Zollinger–Ellison syndrome (ZES) is an exceedingly rare and life‐threatening manifestation of gastrinoma‐related acid hypersecretion.
Agostino Fernicola   +8 more
doaj   +2 more sources

A Rare Case of Renal Gastrinoma

open access: yesScientific World Journal, The, 2009
We present a rare case of renal gastrinoma. To the best of our knowledge, only one case of renal gastrinoma has been reported in the literature so far. An African American male was diagnosed with Zollinger Ellison syndrome at the age of 15 years, when he
Murugesan Manoharan
exaly   +2 more sources

Clinicopathological characteristics and prognosis analysis of gastrinoma based on the SEER database. [PDF]

open access: yesPLoS ONE
Gastrinoma, distinguished by Zollinger-Ellison Syndrome, is a highly unusual neoplasm. However, understanding of its clinicopathological characteristics and survival at the population level is inadequate.
Chenjian Qiu   +6 more
doaj   +2 more sources

Primary hepatic gastrinoma being diagnosed preoperatively: a case report and literature review

open access: yesSurgical Case Reports, 2020
Background A majority of gastrinomas causing Zollinger–Ellison syndrome are located in the duodenum or pancreas. Primary hepatic gastrinomas are rare and difficult to diagnose. We report a rare case of primary hepatic gastrinoma, which could be diagnosed
Shunya Hanzawa   +7 more
doaj   +1 more source

Who were those MEN hiding behind the Ulcers?

open access: yesJournal of the ASEAN Federation of Endocrine Societies, 2020
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disease caused by a mutation in the MEN1 gene. We present a 65-year-old man with MEN1 who has primary hyperparathyroidism, microprolactinoma, meningioma and gastrinoma.
Shazatul Reza Binti Mohd Redzuan   +1 more
doaj   +1 more source

Primary lymph node gastrinoma: a case report and review of the literature

open access: yesWorld Journal of Surgical Oncology, 2020
Background Gastrinoma is a rare form of neuroendocrine neoplasm. The presence of a primary lymph node localization of gastrinoma is a much debated and controversial topic in the literature, as regards whether these cases represent metastatic disease from
Elisabetta Cavalcanti   +5 more
doaj   +1 more source

Gastrinoma hepático primario, presentación de caso extremadamente raro y su resolución quirúrgica, en un hospital de tercer nivel en México

open access: yesCirugía y Cirujanos, 2022
Los gastrinomas son neoplasias neuroendocrinas funcionales raras, y la mayoría se localizan en el duodeno (70-90%) o en el páncreas (2-30%), pero también existen otras localizaciones ectópicas poco comunes.
Rogelio González-López   +7 more
doaj   +1 more source

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