Results 81 to 90 of about 5,629 (238)
ABSTRACT Background Despite the well‐known prognostic role of lymph node metastasis (LNM) in pNETs, less is known about the importance of lymphovascular invasion (LVI) among patients with these tumors. Methods Patients undergoing pancreatectomy for pNET between 2002 and 2020 were identified in the US Neuroendocrine Tumor Study Group database.
Kota Sahara +12 more
wiley +1 more source
Zollinger–Ellison syndrome in a 12-year-old child
The syndrome described by Zollinger and Ellison in 1955 is a rare clinical entity which is even rarer in children. This report describes a 12-year-old boy who presented with refractory peptic ulcer disease which was finally diagnosed to be due to a ...
Abir Lal Nath +5 more
doaj +1 more source
Human insulinoma: Clinical, cellular, and molecular aspects [PDF]
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 +2 more
core
Vergleich Gastrinrezeptorszintigraphie mit 111-In-DTPA-D-Glu1-Minigastrin versus Somatostatinrezeptorszintigraphie mit 111-In-DTPA-D-Phe1-Octreotid bei Patienten mit neuroendokrinen Tumoren. [PDF]
60 Patienten mit neuroendokrinen Tumoren erhielten sowohl eine Somatostatinrezeptorszintigraphie (SRS) als auch eine Gastrinrezeptorszintigraphie mit (GRS) (51 Karzinoide, 3 Gastrinome, 2 Glukagonome, 1 Insulinom, 3 Paragangliome).
Behr, T.M. (Prof. Dr.), Graß, Julia
core +1 more source
Abstract Peptide receptor radionuclide therapy (PRRT) using [177Lu‐DOTA0,Tyr3]octreotate (177Lu‐DOTATATE) represents an established treatment modality for somatostatin receptor‐positive, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumours (GEP NET) of grade 1 or 2.
Jelka Kuiper +4 more
wiley +1 more source
Treatment challenges in and outside a specialist network setting: Pancreatic neuroendocrine tumours [PDF]
Pancreatic Neuroendocrine Neoplasms comprise a group of rare tumours with special biology, an often indolent behaviour and particular diagnostic and therapeutic requirements.
Caplin, Martyn +6 more
core +1 more source
Pediatric Neuroendocrine Tumors in Denmark: Incidence, Management, and Outcome From 1995 to 2020
ABSTRACT Background Neuroendocrine tumors (NETs), although rare, are considered one of the most common gastrointestinal and bronchopulmonary pediatric neoplasms. We aimed to determine the incidence, tumor characteristics, management, and outcome of NETs and explore the role of genetic predisposition, focusing on low and intermediate grade tumors ...
Mona P. Ankerstjerne +7 more
wiley +1 more source
Clinical intestinal transplantation: New perspectives and immunologic considerations [PDF]
Background: Although tacrolimus-based immunosuppression has made intestinal transplantation feasible, the risk of the requisite chronic high- dose treatment has inhibited the widespread use of these procedures.
Abu-Elmagd, K +14 more
core +1 more source
How to treat gastrinomas in patients with multiple endocrine neoplasia type1: surgery or long-term proton pump inhibitors? [PDF]
Masayuki Imamura +2 more
openalex +1 more source

