Results 41 to 50 of about 9,134 (252)

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, Eligijus Poškus, Juozas Stanaitis, Ernesta Rinkevičiūtė, Algirdas Edvardas Tamošiūnas, Kęstutis Strupas   +5 more
doaj   +1 more source

Zollinger–Ellison Syndrome

Video Journal and Encyclopedia of GI Endoscopy, 2014
Abstract Background Zollinger–Ellison (ZE) syndrome is characterized by gastric acid hypersecretion and ulcer disease from autologous gastrin secretion by a gastrinoma. Patient and methods A 43 year old man underwent upper endoscopy for a 6 week history of recurrent nausea, vomiting, heartburn, weight loss, and watery diarrhea. Results Endoscopic
Feriyl Bhaijee, Ruonan Wu, Shou-Jiang Tang   +2 more
openaire   +2 more sources

Síndrome de Zollinger-Ellison

Revista do Colégio Brasileiro de Cirurgiões
The authors report a 49 years old, female patient who have been operated on several times (antrectomy with Billroth II reconstruction, partial gastrectomy with troncular vagotomy and total gastrectomy) in the last 5 years for recurrent ulcer disease ...
Cirilo Luiz de Pardo Mêo Muraro, Hercio Azevedo de Vasconcelos Cunha, Carlos Eduardo de Freitas Júnior   +2 more
doaj   +1 more source

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

American 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, Cooper D. Rodgers, Aldo Fantin, Gulsun Erdag   +3 more
doaj  

Robust Syndrome Extraction via BCH Encoding [PDF]

arXiv, 2023
Quantum data-syndrome (QDS) codes are a class of quantum error-correcting codes that protect against errors both on the data qubits and on the syndrome itself via redundant measurement of stabilizer group elements. One way to define a QDS code is to choose a syndrome measurement code, a classical block code that encodes the syndrome of the underlying ...
arxiv  

Five-Year Long-Term Followup of a Primary Lymph node Gastrinoma: Is a Pancreaticoduodenectomy Justified? [PDF]

, 2009
Background. Gastrinoma-positive lymph nodes and failed localization of the primary tumor during surgical exploration are described. Specialists suppose that these lymph nodes are metastases rather than a primary gastrinoma. Methods.
Article Id, Bernd Jaenigen, Berthold Steinke, Gian Kayser, Oliver Thomusch   +4 more
core   +2 more sources

Treatment of Zollinger-Ellison Syndrome

World Journal of Gastroenterology, 2005
In this article, we have reviewed the main therapeutic measures for the treatment of Zollinger-Ellison syndrome (ZES). Review of the literature was based on computer searches (Pub-Med, Index Medicus) and personal experiences. We have evaluated all the measures now available for treating patients with sporadic gastrinomas or gastrinomas associated with ...
TOMASSETTI, PAOLA, CAMPANA, DAVIDE, PISCITELLI, LYDIA, MAZZOTTA, ELENA, BROCCHI, EMILIO, R. Pezzilli, CORINALDESI, ROBERTO   +6 more
openaire   +4 more sources

Severe and Refractory Peptic Ulcer Disease: The Diagnostic Dilemma [PDF]

, 2005
The recognition of Helicobacter pylori infection as a cause of peptic ulcer disease, medical regimens to eradicate the organism, and the widespread use of proton pump inhibition to suppress gastric acid secretion have revolutionized the management of ...
AF Goddard, AH Soll, AI Lanas, Barbara L. Bass, CC Liu, CW Howden, DC Metz, E Kaneko, EA Lew, EC Ellison, ES Bonapace, F Gibril, F Gibril, F Panzuto, FR Nobels, G Branca, G Cammarota, Grant V. Bochicchio, H Miwa, JA Norton, JA Norton, James L. Guzzo, JC Reynolds, JH Walsh, JL Goldstein, JW Freston, JW Freston, KC Lai, KD Bardhan, KD Bardhan, L Laine, LA Fischbach, Lena M. Napolitano, M Wada, Mona Duncan, O Kisker, P Ruggiero, PD Hung, PK Roy, RF Anda, RJ Hopkins, S Rosenstock, S Verma, T Furuta, VD Corleto, WM Duck   +45 more
core   +1 more source

A rare case of a metastatic neuroendocrine tumor of the pancreas

Бюллетень сибирской медицины, 2021
Aim. To study a rare sporadic case of metastatic gastrinoma associated with mutations in the MEN1 and TSC2 genes in a 25-year-old male.Materials and methods. A retrospective analysis of the history of a 25-year-old patient with sporadic gastrinoma with a
O. I. Kit, V. S. Trifanov, N. N. Timoshkina, E. N. Kolesnikov, D. Y. Gvaldin, N. S. Karnaukhov, D. S. Kutilin, M. Y. Meshcheryakova   +7 more
doaj   +1 more source

Predictors of Mortality in Patients With Multiple Endocrine Neoplasia Type 1

Clinical Endocrinology, EarlyView.
SUMMARY Objective Multiple Endocrine Neoplasia Type 1 (MEN 1) is an autosomal dominant disease predisposing to hyperplasia and neoplasia in diverse endocrine tissues. Patients typically present with endocrine abnormalities before the age of 30 years and have reduced life expectancy.
Jasmine J. Zhu, John R Burgess
wiley   +1 more source