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Background. The aim of this prospectively collected, retrospectively analyzed clinical investigation was to describe "unmasked" clinical symptoms and methods of diagnosis, treatment, and short-term follow-up of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) diagnosed during 1 year in Austria. In 1954, Thorson was the first to describe the clinical "carcinoid syndrome". Carcinoids are derived from Kulchinsky or enterochromaffin cells, which are part of the diffuse neuroendocrine cells of the gut. The incidence of carcinoid tumors is estimated to be 1-2 cases per 100,000 people, accounting for just 0.5% of all malignancies. This website is a service of the National Cancer Institute's Surveillance, Epidemiology, and End Results program and one of several resources for Cancer Registrars.. SEER*RSA Home Gastric neuroendocrine neoplasms (G-NENs) are uncommon, and data on their management is limited. We here investigated the clinicopathological characteristics, surgical and survival outcomes in G-NENs among Chinese. Moreover, we will discuss their prognostic value. From existing databases of the West China Hospital, we retrospectively identified 135 consecutive patients who were surgically Strosberg JR, Weber JM, Feldman M, et al. Prognostic validity of the American Joint Committee on Cancer staging classification for midgut neuroendocrine tumors. J Clin Oncol 2013; 31:420. Shi C, Woltering E, Beyer DT, et al.. Neuroendocrine Tumors of the Colon and Rectum. In: AJCC Cancer Staging Manual, 8th, Amin MB (Ed), AJCC, Chicago 2017. p.401. * Primary sites C165, C166, C168, and C169 are listed in the chapter heading but are not specified in the anatomic subsites in this chapter of the UICC manual; however, they are included in this schema and TNM staged if appropriate histology criteria are met * **Site-Specific Factor 25, Schema Discriminator: EsophagusGEJunction (EGJ)/Stomach The cause of stomach cancer is not yet known. Gastric ulcers are sometimes thou
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