Results 91 to 100 of about 4,463 (213)

Treatment challenges in and outside a specialist network setting: Pancreatic neuroendocrine tumours [PDF]

, 2017
Pancreatic Neuroendocrine Neoplasms comprise a group of rare tumours with special biology, an often indolent behaviour and particular diagnostic and therapeutic requirements.
Caplin, Martyn, Falconi, Massimo, Fusai, Giuseppe K., Lykoudis, Panagis M., Muffatti, Francesca, Partelli, Stefano, Rugge, Massimo   +6 more
core   +1 more source

Síndrome de Zollinger-Ellison: revisión del conocimiento actual

Revista Colombiana de Cirugía, 2016
El síndrome de Zollinger-Ellison se caracteriza por la presencia de úlceras pépticas resistentes al tratamiento que se deben a la hipersecreción ectópica de gastrina por un tumor neuroendocrino, que es el gastrinoma y que resulta en la hipersecreción de ...
Marcelo A. Beltrán
doaj  

The impact of splenectomy on outcomes after distal and total pancreatectomy [PDF]

, 2007
BACKGROUND: Several authors advocate spleen preserving distal pancreatectomy, because of the increased complication rate after splenectomy.METHODS: Postoperative complications and survival after distal and total pancreatectomy, were recorded and ...
Ilias Koukoutsis, Appou Tamijmarane, Riccardo Bellagamba, Simon Bramhall, John Buckels, Darius Mirza   +5 more
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Malignant pancreatic gastrinoma in a maned wolf (Chrysocyon brachyurus): case report

Arquivo Brasileiro de Medicina Veterinária e Zootecnia
A captive 12-year-old female maned wolf (Chrysocyon brachyurus), previously diagnosed with visceral leishmaniasis, developed severe myiasis in the right ear, followed by prostration and death.
T.F. Carvalho, D.N. Frois, H.P. Tinoco, A.T. Pessanha, T.A. Paixão, R.L. Santos   +5 more
doaj   +1 more source

Zollinger-Ellison syndrome associated with neurofibromatosis type 1: a case report

BMC Cancer, 2005
Background Neurofibromatosis type 1 is an autosomal dominant neurocutaneous disorder with characteristic features of skin and central nervous system involvement. Gastrointestinal involvement is rare, but the risk of malignancy development is considerable.
Choi Sung-Kyu, Cho Chol-Kyoon, Kim Hyun-Soo, Joo Young-Eun, Park Chang-Hwan, Kim Jung-Chul, Koh Yang-Seok, Lee Wan-Sik, Rew Jong-Sun, Kim Sei-Jong   +9 more
doaj   +1 more source

Human insulinoma: Clinical, cellular, and molecular aspects [PDF]

, 2018
Insulinoma is the most frequently encountered functioning endocrine pancreatic tumor in humans. In this overview we summarize morphological and clinical features of insulinomas, report about the proinsulin-insulin conversion in normal and neoplastic B ...
Heitz, Philipp, Komminoth, Paul, Roth, Jürgen   +2 more
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A 41-Year-Old Man with Two Types of Metachronous Peptic Ulcer Complication due to Zollinger-Ellison Syndrome—Regression of Pancreatic Primary after Chemoembolization of Hepatic Metastases: A Case Report

Case Reports in Medicine, 2011
Introduction. Gastrinoma should be suspected when the peptic ulcer(s) is postbulbar, multiple, refractory, or recurrent, or ulcer is associated with nephrolithiasis, hypocalcaemia, or erosive esophagitis. The majority of gastrinomas are malignant.
Seyed Saeid Sarkeshikian, Mohammad Reza Ghadir   +1 more
doaj   +1 more source

Oral Pantoprazole for Acid Suppression in the Treatment of Patients with Zollinger-Ellison Syndrome

Canadian Journal of Gastroenterology, 2001
BACKGROUND: The management of patients with gastric acid hypersecretion due to gastrinoma, usually recognized as Zollinger-Ellison syndrome (ZES), was radically changed 10 years ago by the use of proton pump inhibitors.
Barbara Désir, Pierre Poitras
doaj   +1 more source

Gastrinomas [PDF]

Endocrinology and Metabolism Clinics of North America, 2018
Jeffrey A. Norton, Deshka S. Foster, Tetsuhide Ito, Robert T. Jensen   +3 more
openaire   +1 more source

Clinical and genetic characteristics of Multiple Endocrine Neoplasia type 1 (MEN 1) syndrome in a small cohort of Swiss patients [PDF]

, 2015
Multiple endocrine neoplasia type 1 (MEN1) syndrome is a polyglandular autosomal dominant transmitted disease characterized by the combined occurrence of several endocrine gland tumors.
ROSSIER, S.
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