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SHR Neuro Cancer Cardio Lipid Metab Microb

Hoffmann, KM; Furukawa, M; Jensen, RT.
Duodenal neuroendocrine tumors: Classification, functional syndromes, diagnosis and medical treatment.
Best Pract Res Clin Gastroenterol. 2005; 19(5):675-697 Doi: 10.1016/j.bpg.2005.05.009
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Leading authors Med Uni Graz
Hoffmann Karl Martin
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Abstract:
Duodenal neuroendocrine tumors (NETs) comprise 2-3% of all GI endocrine tumors and are increasing in frequency. These include gastrinomas, somatostatinomas, nonfunctional NETs, gangliocytic paragangliomas, and poorly differentiated NE carcinomas. Although, the majority are nonfunctional, these tumors are a frequent cause of Zollinger-Ellison syndrome and can cause other clinical hormonal syndromes (carcinoid, Cushing's, etc.). In this chapter, their epidemiology, clinical aspects, localization, diagnosis and medical treatment are reviewed including the latest advances in each area.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Age Distribution -
Aged -
Aged, 80 and over -
Biopsy, Needle -
Carcinoid Tumor - classification
Combined Modality Therapy - classification
Duodenal Neoplasms - classification
Duodenoscopy - methods
Female - methods
Humans - methods
Immunohistochemistry - methods
Incidence - methods
Male - methods
Middle Aged - methods
Neoplasm Staging - methods
Neuroendocrine Tumors - classification
Prognosis - classification
Risk Assessment - classification
Sex Distribution - classification
Somatostatinoma - classification
Survival Analysis - classification
United States - epidemiology
Zollinger-Ellison Syndrome - classification

Find related publications in this database (Keywords)
duodenal carcinoid
carcinoid
gastrinoma
Zollinger-Ellison syndrome
somatostatinoma
MEN I
gangliocytic paraganglioma
von Recklinghausen's disease
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