نتایج جستجو برای: insulinoma

تعداد نتایج: 2143  

Journal: :European journal of endocrinology 2001
C Letizia G Tamburrano P Alo A Paoloni C Caliumi E Marinoni R di Iorio E d'Erasmo

BACKGROUND It has been demonstrated that adrenomedullin, a newly discovered peptide, affects the release of insulin from pancreatic islets cells, suggesting a role in the insulin-regulating system. OBJECTIVE To investigate whether adrenomedullin secretion is modified in patients with insulin-secreting islet cell tumours. DESIGN The study was performed in nine patients with surgically treate...

Journal: :European journal of endocrinology 2010
Gregory S Y Ong David E Henley David Hurley J Harvey Turner Phillip G Claringbold P Gerry Fegan

OBJECTIVE Hypoglycaemia poses a significant management challenge in patients with unresectable functional malignant insulinoma. Novel agents such as mammalian target of rapamycin (mTOR) inhibitors and radiolabelled peptides may be effective where there is failure of conventional therapy. DESIGN We present the cases of two men diagnosed with inoperable malignant insulinoma and hepatic metastas...

2015
Hanjun Guan K. Martin Chow Eunsuk Song Nirmal Verma Florin Despa Louis B. Hersh Jie Zheng

Amyloid formation and mitochondrial dysfunction are characteristics of type 2 diabetes. The major peptide constituent of the amyloid deposits in type 2 diabetes is islet amyloid polypeptide (IAPP). In this study, we found that pitrilysin, a zinc metallopeptidase of the inverzincin family, degrades monomeric, but not oligomeric, islet amyloid polypeptide in vitro. In insulinoma cells when pitril...

2016
Eun Byul Kwon Hwal Rim Jeong Young Seok Shim Hae Sang Lee Jin Soon Hwang

Multiple endocrine neoplasia (MEN) mutation is an autosomal dominant disorder characterized by the occurrence of parathyroid, pancreatic islet, and anterior pituitary tumors. The incidence of insulinoma in MEN is relatively uncommon, and there have been a few cases of MEN manifested with insulinoma as the first symptom in children. We experienced a 9-year-old girl having a familial MEN1 mutatio...

2015
Ersin Borazan Alper Aytekin Latif Yilmaz Muhsin Elci Mehmet Salih Karaca Selim Kervancioglu Ahmet Abdulhalik Balik

Insulinoma is the most frequently seen functional pancreatic neuroendocrine tumor. The incidence of multifocal insulinoma is lower than 10%. Its treatment is direct or laparoscopic excision. The present case was examined with the findings of hypoglycemia and hypercalcemia, and as there was high insulin and C-peptide levels the initial diagnosis was insulinoma. The case was investigated in terms...

2010
Robert Bränström Erik Berglund Pontus Curman Lars Forsberg Anders Höög Lars Grimelius Per-Olof Berggren Per Mattsson Per Hellman Lisa Juntti-Berggren

INTRODUCTION Non-insulinoma pancreatogenous hypoglycemic syndrome is a rare disorder among adults, and, to our knowledge, only about 40 cases have been reported in the literature. CASE PRESENTATION The patient is a previously healthy 35-year-old Caucasian man. His symptoms began four years ago when he suddenly felt weakness in his legs and started sweating for unknown reasons. The symptoms wo...

2015
Caroline Spenlé Isabelle Gasser Falk Saupe Klaus-Peter Janssen Christiane Arnold Annick Klein Michael van der Heyden Jérome Mutterer Agnès Neuville-Méchine Marie-Pierre Chenard Dominique Guenot Iréne Esposito Julia Slotta-Huspenina Noona Ambartsumian Patricia Simon-Assmann Gertraud Orend

The extracellular matrix (ECM) molecule tenascin-C (TNC) promotes tumor progression. This has recently been demonstrated in the stochastic murine RIP1-Tag2 insulinoma model, engineered to either express TNC abundantly or to be devoid of TNC. However, our knowledge about organization of the TNC microenvironment is scant. Here we determined the spatial distribution of TNC together with other ECM ...

Journal: :JOP : Journal of the pancreas 2006
Abel Gonzalez-Gonzalez Jose María Recio-Cordova

CONTEXT Insulinomas may be regarded as potentially malignant. A long follow-up period is needed to detect any possible recurrence, even if the initial diagnosis was of a benign insulinoma. CASE REPORT We present the case of a 76-year-old woman with liver metastases due to a malignant insulinoma, which had been diagnosed as benign after its complete removal 9 years earlier. CONCLUSIONS This ...

2014
ZBIGNIEW KRZYSZTOF KAMOCKI NATALIA ANNA WODYŃSKA ANNA PRYCZYNICZ

Neuroendocrine tumors constitute a group of heterogeneous neoplasms, both those that are clinically asymptomatic and those which present with an array of symptoms. This variable clinical manifestation and unsatisfactory detection rate on diagnostic imaging make preoperative diagnosis particularly challenging. Insulinoma is a rare tumor originating from insulin-synthetizing pancreatic beta cells...

Journal: :World Journal of Surgical Oncology 2009
Edward Alabraba Simon Bramhall Brendan O'Sullivan Brinder Mahon Philippe Taniere

BACKGROUND Gastrointestinal stromal tumours (GIST) frequently occur in patients with neurofibromatosis type 1 (NF-1). It has been reported that GIST may co-exist with pancreatic endocrine tumors but this has only been in association with NF-1. CASE PRESENTATION A 76 year old woman presented with a 12 month history of hypoglycaemia symptoms. Abdominal CT scan demonstrated a 13 mm insulinoma lo...

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