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University of the Chinese Academy of Sciences, Beijing, China
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Introduction Neuroendocrine neoplasms (NENs) arise from neuroendocrine systems and often occur in tissues, such as lung, pancreas and pituitary tissues ( Ohki et al. 2014 , Gao et al. 2018 ). However, due to the low incidence and the lack
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Introduction Pancreatic neuroendocrine neoplasms (panNENs) are considered rare malignancies despite a steady increase in their incidence as shown by recent epidemiological studies ( Dasari et al. 2017 ). PanNENs are considered slow
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Introduction Functional imaging has become critical for gastro–entero–pancreatic neuroendocrine neoplasm (GEP NEN) ( Krenning et al . 1994 , Baudin 2007 ). Somatostatin receptors (sst) are expressed by these tumors, and somatostatin receptor
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‘Vita-Salute’ San Raffaele University, Milan, Italy
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‘Vita-Salute’ San Raffaele University, Milan, Italy
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OR pancreatic neuroendocrine neoplasm OR pancreatic neuroendocrine neoplasms OR Adenomas, Islet Cell OR Islet Cell Adenoma OR Islet Cell Adenomas OR Islet Cell Tumor OR Islet Cell Tumors OR Tumor, Islet Cell OR Tumors, Islet Cell OR Island Cell Tumor
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Introduction Small intestinal neuroendocrine tumours (SI-NETs) are rare and mostly slow-growing neoplasms originating from the enterochromaffin (EC) cells of the intestine ( de Herder 2005 , Yao et al . 2008 ). EC cells are chemo- and
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Department of Pathology, Department of Pathology, Department of General, Department of Gastroenterology and Endocrinology, Department of Endocrinology, Department of General and Abdominal Surgery, Department of Gastroenterology and Endocrinology, Department of Hepatology and Gastroenterology, Department of Pathology, Institute of Pathology, University of Kiel, Michaelisstr. 11, 24105 Kiel, Germany
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Department of Pathology, Department of Pathology, Department of General, Department of Gastroenterology and Endocrinology, Department of Endocrinology, Department of General and Abdominal Surgery, Department of Gastroenterology and Endocrinology, Department of Hepatology and Gastroenterology, Department of Pathology, Institute of Pathology, University of Kiel, Michaelisstr. 11, 24105 Kiel, Germany
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Introduction Neuroendocrine tumors (NETs) of the stomach, intestine, and pancreas are heterogeneous, as far as their morphology, function, and biology are concerned. The WHO classification therefore distinguishes the gastroenteropancreatic NETs
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patients had a history of primary pulmonary neuroendocrine neoplasms. Clinical information including sex, age, type of surgery, clinical history, the presence of distant metastases, and follow-up findings was collected by consulting clinical charts. This
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Introduction Neuroendocrine (carcinoid) tumors (NETs) are neoplasms of the endocrine system arising predominantly in the gastrointestinal (GI) tract and respiratory system. These neoplasms originate in cells of the diffuse neuroendocrine system, and
Department of Clinical Sciences and Community Health (DISCCO), Laboratory of Endocrine and Metabolic Research, Department of Biosciences, Endocrinology Unit, University of Milan, Milan, Italy
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Department of Clinical Sciences and Community Health (DISCCO), Laboratory of Endocrine and Metabolic Research, Department of Biosciences, Endocrinology Unit, University of Milan, Milan, Italy
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a model in cancer research, focusing on potential applications in neuroendocrine tumors (NETs). Zebrafish as a cancer model Although fish do not have certain organs found in mammals (breast, prostate, and lung), zebrafish spontaneously develops
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501 – 513 . ( doi:10.1056/NEJMoa1003825 ) 19 Rindi G Arnold R 2010 Nomenclature and classification of neuroendocrine neoplasms of the digestive system. In World Health Organization Classification of Tumours of the Digestive