Results 41 to 50 of about 1,249 (168)

European Neuroendocrine Tumor Society (ENETS) 2022 Guidance Paper for Carcinoid Syndrome and Carcinoid Heart Disease

open access: yes, 2022
Journal of Neuroendocrinology, Volume 34, Issue 7, July 2022.
Simona Grozinsky‐Glasberg   +13 more
wiley   +1 more source

Life-threatening diarrhea in neuroendocrine tumors: two case reports

open access: yesJournal of Medical Case Reports, 2021
Background Neuroendocrine tumors are rare, heterogeneous neoplasms that produce a wide variety of clinical symptoms. Diarrhea in neuroendocrine tumors is incredibly common and is usually benign in nature.
Emma Gordon   +9 more
doaj   +1 more source

An Insight on Functioning Pancreatic Neuroendocrine Neoplasms

open access: yesBiomedicines, 2023
Pancreatic neuroendocrine neoplasms (PanNENs) are rare neoplasms arising from islets of the Langerhans in the pancreas. They can be divided into two groups, based on peptide hormone secretion, functioning and nonfunctioning PanNENs.
Michele Bevere   +5 more
doaj   +1 more source

Vipoma asociado a dermatomiosistis, tiroiditis de Hashimoto y pancreatitis autoinmune (síndrome poliglandular tipo 3C)

open access: yes, 2022
A 72-year-old woman with chronic secretory diarrhea, oropharyngeal dysphagia, proximal muscle weakness, dermal involvement and multinodular goiter; with images and auxiliary studies compatible with a benign VIPoma associated with dermatomyositis and a ...
García-Ramos, Hugo Michael   +1 more
core   +2 more sources

VIPoma in retroperitoneum of elderly, cause of chronic diarrhea in uncommon location [PDF]

open access: yes, 2015
La diarrea crónica secretora es una entidad frecuente. Las causas son múltiples, por lo que llegar al diagnóstico definitivo puede resultar demorado con las complicaciones que esto ocasiona en el estado general del paciente.
Miranda, Gonzalo, Luna, Laura
core   +1 more source

Management of the hormonal syndrome of neuroendocrine tumors

open access: yesArchives of Medical Science, 2016
Gastroenteropancreatic neuroendocrine tumors (GEP/NET) are unusual and relatively rare neoplasms that present many clinical challenges. They characteristically synthesize, store and secrete a variety of peptides and neuroamines which can lead to the ...
Paweł Gut   +10 more
doaj   +1 more source

Clinical Characteristics and Management of Functional Pancreatic Neuroendocrine Neoplasms: A Single Institution 20-Year Experience with 286 Patients

open access: yesInternational Journal of Endocrinology, 2020
Background. Functional pancreatic neuroendocrine neoplasms (PanNENs) are very rare disorders but have complex spectrum, including insulinoma, gastrinoma, glucagonoma, somatostatinoma, and VIPoma.
Yuqing Qu   +10 more
doaj   +1 more source

Endoscopic Ultrasound for the Management of Pancreatic Neuroendocrine Tumors: Diagnosis, Treatment, and Future Perspectives

open access: yesJournal of Gastroenterology and Hepatology, Volume 41, Issue 4, Page 1173-1190, April 2026.
ABSTRACT Pancreatic neuroendocrine tumors (PanNETs) are increasingly diagnosed, reflecting greater clinical awareness, improved imaging, and revised classification. This review summarizes evidence on epidemiology, diagnostic workup, and endoscopic ultrasound (EUS)–guided management of PanNETs, encompassing diagnostic evaluation, tissue acquisition, and
Angelo Bruni   +7 more
wiley   +1 more source

Rare Cases of Pediatric Vasoactive Intestinal Peptide Secreting Tumor With Literature Review: A Challenging Etiology of Chronic Diarrhea

open access: yesFrontiers in Pediatrics, 2020
Vasoactive intestinal peptide (VIP) secreting tumor (VIPoma) is a rare disease, presenting with profuse diarrhea, electrolyte imbalance, and possibly fatal outcome.
Pai-Jui Yeh   +9 more
doaj   +1 more source

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