Results 61 to 70 of about 53,065 (244)

The impact of re‐characterizing metastatic pancreatic neuroendocrine tumors: A prospective study

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract The biology of metastatic pancreatic neuroendocrine tumors (panNET) may alter over time. It remains to be defined if, how, and when this patient group should be recommended to re‐evaluate the characteristics of their disease. This prospective single‐center, longitudinal cohort study at Uppsala University Hospital, Sweden (NCT03130205 ...
Kazhan Mollazadegan   +9 more
wiley   +1 more source

Fragility fractures in well‐differentiated gastroenteropancreatic neuroendocrine tumors: Results from a multicentered retrospective study

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract Patients with gastroenteropancreatic–neuroendocrine tumors (GEP‐NETs) may present skeletal fragility that might be related to multiple factors, including bone metastases, vitamin D deficiency, hormone secretion, and disease treatments. This study examines the prevalence and determinants of fragility fractures in low grading (G1‐G2) GEP‐NETs ...
Alessandro Brunetti   +15 more
wiley   +1 more source

Primary renal well‐differentiated neuroendocrine tumors with lymph node metastasis: A case report and literature review

open access: yesIJU Case Reports, Volume 8, Issue 3, Page 202-205, May 2025.
Introduction Well‐differentiated neuroendocrine tumors of the kidney are rare and generally less aggressive than renal cell carcinoma, although metastasis is still present at the time of diagnosis. Surgical resection remains the preferred treatment, even in cases with lymph node metastases.
Huy‐Hoang Nguyen   +3 more
wiley   +1 more source

An unusual case of multiple myeloma [PDF]

open access: yes, 2013
The case concerns the unusual presentation of a non-secretory multiple myeloma with diarrhoea secondary to large bowel infiltration. In December 2009, a 74-year-old lady presented to hospital and complained of a two year history of intermittent ...
Delicata, Julian, Farrugia, Daniel
core  

Telotristat ethyl in carcinoid syndrome: safety and efficacy in the TELECAST phase 3 trial [PDF]

open access: yes, 2018
Telotristat ethyl, a tryptophan hydroxylase inhibitor, was efficacious and well tolerated in the phase 3 TELESTAR study in patients with carcinoid syndrome (CS) experiencing ≥4 bowel movements per day (BMs/day) while on somatostatin analogs (SSAs ...
Anthony, Lowell B.   +17 more
core   +2 more sources

Experiences and Fundamental Care Needs in Patients With Small Intestinal Neuroendocrine Tumours—An Interview Study in a Surgical Context

open access: yesJournal of Advanced Nursing, Volume 81, Issue 4, Page 2061-2071, April 2025.
ABSTRACT Aims The study aimed to describe patients' fundamental care needs and their experiences of nursing care, throughout surgical treatment of small intestinal neuroendocrine tumours. Design A qualitative descriptive study was performed. Methods Patients' interviews (n = 19) were conducted in Sweden from May 2021 to January 2022 and analysed using ...
Frida Olsson   +2 more
wiley   +1 more source

THE MALIGNANT CARCINOID SYNDROME ASSOCIATED WITH A METASTASIZING BRONCHIAL ADENOMA

open access: closedThe Journal of Thoracic and Cardiovascular Surgery, 1962
Robert J. McConaghie
openaire   +3 more sources

Quadruple Valve Replacement for Carcinoid Heart Disease

open access: yesBrazilian Journal of Cardiovascular Surgery
Introduction: Carcinoid heart disease most frequently involves the tricuspid or, more rarely, the pulmonary valve and presents with right heart failure as 5-HT is metabolized by the lung. Left-sided valve involvement is quite rare.
Syed Saleem Mujtaba, Stephen Clark
doaj   +1 more source

Considerations concerning a tailored, individualized therapeutic management of patients with (neuro)endocrine tumours of the gastrointestinal tract a [PDF]

open access: yes, 2004
Endocrine tumours of the gastrointestinal tract and pancreas may present at different disease stages with either hormonal or hormone-related symptoms/syndromes, or without hormonal symptoms. They may occur either sporadically or as part
Eijck, C.H.J. (Casper) van   +3 more
core  

Primary Hepatic Neuroendocrine Carcinoma Associated With Carcinoid Syndrome and Pellagra: A Case Report

open access: yesLiver International Communications, Volume 6, Issue 1, March 2025.
ABSTRACT Carcinoid tumours are slow‐growing neuroendocrine neoplasms mainly affecting the gastrointestinal tract, the respiratory tree, ovaries and kidneys. Approximately 20% of patients with carcinoid tumour are affected by carcinoid syndrome, characterised by chronic diarrhoea and/or flushing in the presence of systemically elevated levels of ...
Abdelmounem Eltayeb Abdo   +7 more
wiley   +1 more source

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