keyword
https://read.qxmd.com/read/38605021/gastric-neuroendocrine-neoplasms
#1
REVIEW
Giuseppe Lamberti, Francesco Panzuto, Marianne Pavel, Dermot O'Toole, Valentina Ambrosini, Massimo Falconi, Rocio Garcia-Carbonero, Rachel P Riechelmann, Guido Rindi, Davide Campana
Gastric neuroendocrine neoplasms (gNENs) display peculiar site-specific features among all NENs. Their incidence and prevalence have been rising in the past few decades. gNENs comprise gastric neuroendocrine carcinomas (gNECs) and gastric neuroendocrine tumours (gNETs), the latter further classified into three types. Type I anatype II gNETs are gastrin-dependent and develop in chronic atrophic gastritis and as part of Zollinger-Ellison syndrome within a multiple endocrine neoplasia type 1 syndrome (MEN1), respectively...
April 11, 2024: Nature Reviews. Disease Primers
https://read.qxmd.com/read/38590468/severe-hypomagnesemia-caused-by-proton-pump-inhibitors-in-a-patient-with-an-ostomy
#2
Kabeer Ali, Aleem A Ali, Vishal Jaikaransingh
Proton pump inhibitors (PPIs) are commonly used for many gastrointestinal issues, such as gastroesophageal reflux disease (GERD), peptic ulcer disease, and Zollinger-Ellison syndrome. Many patients are on life-long daily therapy with this class of medications. The adverse effects of long-term use of PPI have been studied, and over the last two decades, a link between hypomagnesemia and PPI has been established. In addition, other electrolyte derangements can also ensue, such as hypokalemia and hypocalcemia...
March 2024: Curēus
https://read.qxmd.com/read/38531512/recurrent-duodenal-ulceration-more-than-simple-peptic-ulcer-disease
#3
JOURNAL ARTICLE
Govind Kallumkal, Justin McCallen, Michael Contarino
No abstract text is available yet for this article.
March 24, 2024: Gastroenterology
https://read.qxmd.com/read/38524517/sporadic-gastrinoma-with-refractory-benign-esophageal-stricture-a-case-report
#4
Qian-Nan Chen, Bing-Qing Bai, Yan Xu, Qiao Mei, Xiao-Chang Liu
BACKGROUND: Gastrinoma is characterized by an excessive release of gastrin, leading to hypersecretion of gastric acid, subsequently resulting in recurrent peptic ulcers, chronic diarrhea, and even esophageal strictures. This case report aims to improve awareness and facilitate early diagnosis and treatment of gastrinoma by presenting a rare case of gastrinoma with refractory benign esophageal stricture (RBES). Additionally, it highlights the persistent challenges that gastroenterologists encounter in managing RBES...
March 6, 2024: World Journal of Clinical Cases
https://read.qxmd.com/read/38447521/sporadic-zollinger-ellison-syndrome-in-a-patient-with-isolated-mesenteric-gastrinoma
#5
Boubacar Efared, Elh I M Tassiou, Aïchatou Balaraba Abani Bako, Idrissa Boubacar, Habiba Salifou Boureima, Hassan Nouhou
INTRODUCTION: Zollinger-Ellison syndrome (ZES) is due to a gastrin-producing neuroendocrine tumor (gastrinoma) with subsequent gastric acid hypersecretion, gastroesophageal reflux disease (GERD), peptic ulcers, and chronic diarrhea. CASE PRESENTATION: A 40-year old patient presented with epigastric pain associated with diarrhea evolving for 10 years, he has been treated by acid-suppressive medications without substantial clinical improvement. Gastro-duodenal endoscopy was performed with gastric biopsies that showed peptic ulcerations, a serum gastrin assay that showed high levels exceeding 10 times the upper limit of the normal range...
March 5, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38378461/duodenal-gastrinoma-case-report
#6
JOURNAL ARTICLE
Z Adamová, M Chrostek, T Dvořák, E Rada
INTRODUCTION: In our text, we want to highlight a rare diagnosis. CASE REPORT: A 54-year-old obese, hypertensive male smoker had been investigated for intermittent abdominal pain for 12 years. The first gastroscopy for a bleeding ulcer was conducted in 2010. In the subsequent years, repeated gastroscopies revealed variable involvement from the esophagus to the duodenum. Capsule enteroscopy did not provide further specification of the diagnosis. The patient underwent colonoscopy and MRI enterography multiple times, with no unequivocal pathological findings...
2024: Rozhledy V Chirurgii: Měsíčník Československé Chirurgické Společnosti
https://read.qxmd.com/read/38299632/the-cckoma-syndrome-and-its-relation-to-the-zollinger-ellison-syndrome-a-diagnostic-challenge
#7
REVIEW
Jens F Rehfeld
OBJECTIVE: Among patients with enteropancreatic neuroendocrine tumor syndromes only one case with a cholecystokinin (CCK) secreting tumor has been reported. She had significant hyperCCKemia leading to a specific syndrome of severe diarrheas, weight loss, repeated duodenal ulcers and a permanently contracted gallbladder with gallstones. There are, however, reasons to believe that further CCKomas exist, for instance among Zollinger-Ellison patients with normal plasma gastrin concentrations...
February 1, 2024: Scandinavian Journal of Gastroenterology
https://read.qxmd.com/read/38269224/chronic-use-of-proton-pump-inhibitors-a-potential-link-to-amino-acid-deficiency-and-the-development-of-depression
#8
Jeevan J Murthy, Sarah Hughes, Colin Travis, Ankit Chalia, Samira Khan, Michael Ang-Rabanes, Raja Mogallapu
In recent years, the gut-brain axis (GBA) has been implicated in several vital physiological processes, including digestion, immunity, inflammation, and mood regulation. Disruption of this network is tied to the development of several pathological conditions, including mood disorders, inflammatory bowel diseases, and dementia. Proton pump inhibitors (PPI) are among the most utilized and easily accessible medications worldwide. Although they are effective at treating conditions, including gastroesophageal reflux disorder (GERD), peptic ulcer disease, Zollinger-Ellison syndrome, and erosive esophagitis, PPIs have several mechanisms that may precipitate protein and, thus, amino acid malnutrition...
December 2023: Curēus
https://read.qxmd.com/read/38150171/pbpk-modeling-to-predict-the-pharmacokinetics-of-pantoprazole-in-different-cyp2c19-genotypes
#9
JOURNAL ARTICLE
Chang-Keun Cho, Eunvin Ko, Ju Yeon Mo, Pureum Kang, Choon-Gon Jang, Seok-Yong Lee, Yun Jeong Lee, Jung-Woo Bae, Chang-Ik Choi
Pantoprazole is used to treat gastroesophageal reflux disease (GERD), maintain healing of erosive esophagitis (EE), and control symptoms related to Zollinger-Ellison syndrome (ZES). Pantoprazole is mainly metabolized by cytochrome P450 (CYP) 2C19, converting to 4'-demethyl pantoprazole. CYP2C19 is a genetically polymorphic enzyme, and the genetic polymorphism affects the pharmacokinetics and/or pharmacodynamics of pantoprazole. In this study, we aimed to establish the physiologically based pharmacokinetic (PBPK) model to predict the pharmacokinetics of pantoprazole in populations with various CYP2C19 metabolic activities...
December 27, 2023: Archives of Pharmacal Research
https://read.qxmd.com/read/38111491/severe-esophageal-stricture-after-perforation-and-necrotizing-esophagitis-unusual-presentation-of-a-duodenal-gastrinoma
#10
Sunao Ito, Ryo Ogawa, Masayuki Komura, Shunsuke Hayakawa, Tomotaka Okubo, Hiroyuki Sagawa, Tatsuya Tanaka, Akira Mitsui, Satoru Takahashi, Shuji Takiguchi
Gastrinomas are pancreatic or duodenal endocrine tumors that secrete excess gastrin, which causes gastroesophageal reflux disease, peptic ulcers, and chronic diarrhea. Due to the rarity of the disease, nonspecific symptoms, and the outstanding effect of proton pump inhibitors, diagnosing gastrinomas is difficult. Here, we present the case of a 58-year-old woman who had a duodenal gastrinoma that caused rare but critical events, including esophageal perforation, necrotizing esophagitis, and severe esophageal stricture...
December 2023: Journal of Surgical Case Reports
https://read.qxmd.com/read/38062290/management-of-gastric-neuroendocrine-tumors-a-review
#11
REVIEW
Caitlin Sok, Pranay S Ajay, Vasileios Tsagkalidis, David A Kooby, Mihir M Shah
Gastric neuroendocrine tumors (G-NET) are rare tumors arising from enterochromaffin-like cells of the gastric mucosa. They belong to a larger group called gastroenteropancreatic neuroendocrine tumors and are classified as low, intermediate, or high-grade tumors based on their proliferative indices. They are further categorized into three subtypes based on their morphologic characteristics, pathogenesis, and behavior. Types 1 and 2 tumors are characterized by elevated serum gastrin and are usually multifocal...
December 7, 2023: Annals of Surgical Oncology
https://read.qxmd.com/read/38025843/complete-esophageal-obstruction-a-rare-complication-of-zollinger-ellison-syndrome
#12
Blake Bentley, Fadi Chanaa, Steven Clayton
Complete esophageal obstruction (CEO) is a rare phenomenon usually observed after receiving head and neck radiation. Zollinger-Ellison syndrome (ZES) is typically associated with minimal esophageal morbidity because of advancements in antisecretory medications. There are currently no documented reports of CEO in patients with ZES. Although surgeries are available for the treatment of CEO, there is no established method for endoscopic lumen restoration, given its rarity. This case documents potential sequala of modern-day patients with ZES...
November 2023: ACG Case Reports Journal
https://read.qxmd.com/read/37868662/esophageal-perforation-unveiling-the-diagnosis-of-zollinger-ellison-syndrome
#13
Mohammed R Shaik, Nishat A Shaik, Vithura Kunarathnam, Zaid Bilgrami, Erika Wheeler, Shien Hu
Gastrinomas are the most common neuroendocrine tumors worldwide and cause a clinical syndrome known as Zollinger-Ellison Syndrome (ZES). Increased acid production resulting from elevated gastrin levels contributes to symptoms such as abdominal pain, heartburn, and diarrhea. However, the non-specificity and overlap in the symptoms with idiopathic peptic ulcer disease and gastroesophageal reflux disease (GERD) can lead to delayed diagnosis. In this case, we describe a patient with a past medical history of GERD and a perforated gastric ulcer who continued to experience symptoms of dyspepsia and had a subsequent esophageal perforation, despite H...
2023: Journal of Community Hospital Internal Medicine Perspectives
https://read.qxmd.com/read/37867522/multiple-endocrine-neoplasia-type-1-with-zollinger-ellison-syndrome-clinicopathological-analysis-of-a-japanese-family-with-focus-on-menin-immunohistochemistry
#14
JOURNAL ARTICLE
Noriko Kimura, Yasuji Hirata, Nozomu Iwashiro, Hiroshi Kijima, Shinobu Takayasu, Satoshi Yamagata, Satoru Sakihara, Shinya Uchino, Masanori Ohara
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of multiple epithelial neuroendocrine tumors (NETs) and non-NETs in various organs. MEN1 encodes a 610-amino acid-long tumor suppressor protein, menin. The optimal treatment for multiple tumors, identification of the most critical tumors for patient prognosis, and menin immunohistochemistry findings remain controversial. Therefore, we aimed to elucidate these issues through a histological analysis of tumors and tumor-like lesions in a Japanese family, comprising a father and his two sons, who had MEN1 with Zollinger-Ellison syndrome (ZES)...
2023: Frontiers in Endocrinology
https://read.qxmd.com/read/37737818/aga-clinical-practice-update-on-the-epidemiology-evaluation-and-management-of-exocrine-pancreatic-insufficiency-expert-review
#15
David C Whitcomb, Anna M Buchner, Chris E Forsmark
DESCRIPTION: Exocrine pancreatic insufficiency (EPI) is a disorder caused by the failure of the pancreas to deliver a minimum/threshold level of specific pancreatic digestive enzymes to the intestine, leading to the maldigestion of nutrients and macronutrients, resulting in their variable deficiencies. EPI is frequently underdiagnosed and, as a result, patients are often not treated appropriately. There is an urgent need to increase awareness of and treatment for this condition. The aim of this American Gastroenterological Association (AGA) Clinical Practice Update Expert Review was to provide Best Practice Advice on the epidemiology, evaluation, and management of EPI...
September 20, 2023: Gastroenterology
https://read.qxmd.com/read/37731553/typical-zollinger-ellison-syndrome-atypical-location-of-gastrinoma-and-absence-of-hypergastrinemia-a-case-report-and-review-of-literature
#16
Jin-Ming Zhang, Chu-Wei Zheng, Xiao-Wen Li, Zhi-Yun Fang, Mu-Xin Yu, Hai-Yan Shen, Xia Ji
BACKGROUND: Zollinger-Ellison syndrome (ZES) results from hypersecretion of gastrin from pancreatic or duodenal neuroendocrine tumors, commonly referred to as gastrinomas. The high levels of gastrin lead to a typical presentation involving watery diarrhea and multiple ulcers in the duodenum. Here, we have presented the rare case of a patient with ZES and absence of hypergastrinemia as well as an atypical location of gastrinoma. CASE SUMMARY: A 72-year-old woman presented with the typical clinical manifestations of ZES, including upper abdominal pain, significant watery diarrhea, and acidic liquid vomitus...
September 16, 2023: World Journal of Clinical Cases
https://read.qxmd.com/read/37700944/a-rare-case-of-hepatic-gastrinoma
#17
Eli A Zaher, Shayet Hossain Eshan, Parth Patel, Zahin Islam Rafa, Daria Zaher
Zollinger-Ellison syndrome (ZES) is a rare condition caused by gastrin-secreting neuroendocrine tumors known as gastrinomas. We present a case of hepatic ZES presenting as upper gastrointestinal (GI) bleeding in a 70-year-old female. Initial evaluation revealed the patient to be in severe sepsis with septic shock secondary to a urinary tract infection, and her hospitalization was complicated by hematemesis and melena in the setting of multiple duodenal ulcers. Subsequent investigations, including elevated gastrin levels and a somatostatin receptor scan, confirmed the diagnosis of gastrinoma...
August 2023: Curēus
https://read.qxmd.com/read/37688510/acth-secreting-pancreatic-neuroendocrine-neoplasms-a-case-series
#18
JOURNAL ARTICLE
Taymeyah Al-Toubah, Eleonora Pelle, Julie Hallanger-Johnson, Mintallah Haider, Jonathan Strosberg
Ectopic Cushing's syndrome (CS) occurs rarely in patients with pancreatic neuroendocrine neoplasms. Early recognition of symptoms is critical given the high morbidity and mortality associated with CS. A database of pancreatic neuroendocrine neoplasms (NENs) seen at the Moffitt Cancer Center between 1/2008 and 4/2022 was reviewed and cases of ectopic CS were identified. Information was extracted on tumor characteristics, clinical signs and symptoms, therapies, and outcomes. Thirteen cases were identified, ranging in age from 16 to 65 years at the initial time of diagnosis (median 42)...
October 2023: Journal of Neuroendocrinology
https://read.qxmd.com/read/37651247/over-30-years-of-omeprazole
#19
JOURNAL ARTICLE
Praveen Sharma
BACKGROUND: In the last 3 decades, omeprazole has proved its mettle in managing acid peptic diseases (APDs). It has established itself as the first line of therapy for duodenal and gastric ulcers, gastroesophageal reflux disease (GERD), ulcers due to nonsteroidal anti-inflammatory drugs (NSAID), and Zollinger-Ellison syndrome (ZES). OBJECTIVES: The purpose of this literature review is to assess the effectiveness of omeprazole as compared to the other proton pump inhibitors (PPIs) currently in use and its safety and efficacy in special populations, including the pediatric and geriatric populations...
August 2023: Journal of the Association of Physicians of India
https://read.qxmd.com/read/37539518/multiple-endocrine-neoplasia-type-1-and-zollinger-ellison-syndrome
#20
JOURNAL ARTICLE
Modesto Varas Lorenzo, Fernando Muñoz Agel
Retrospective study of three cases of MEN type 1 and ZES, to compare with one similar case in publication of The Spanish J of Gastroenterol: MEN-1 and ZES for pancreatic gastrinoma.
August 4, 2023: Revista Española de Enfermedades Digestivas
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