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作 者:Elisabetta Dell’Unto Maria Rinzivillo Gianluca Esposito Elsa Iannicelli Daniela Prosperi Francesco Panzuto Bruno Annibale
机构地区:[1]Department of Medical-Surgical Sciences and Translational Medicine,Sapienza University of Rome,Rome,Italy [2]Digestive Disease Unit-ENETS Center of Excellence,Sant’Andrea University Hospital,Italy [3]Radiology Unit-ENETS Center of Excellence,Sant'Andrea University Hospital,Rome,Italy [4]Nuclear Medicine Unit-ENETS Center of Excellence,Sant’Andrea University Hospital,Rome,Italy
出 处:《Gastroenterology Report》2024年第1期805-807,共3页胃肠病学报道(英文)
基 金:supported by Sapienza University of Rome[Grant Ateneo 2022 RM12218161A53B1D].
摘 要:Background Gastric neuroendocrine tumors(g-NETs)are classified into:Type 1,associated with chronic atrophic gastritis(CAG);Type 2,related to Zollinger-Ellison Syndrome/Multiple Endocrine Neoplasia Type 1;and sporadic Type 3[1].Type 1,the most common,typically presents as small,well-differentiated tumors with excellent survival[1].Tumor size and gender are important prognostic factors in Type 1 g-NETs,with a controversial prognostic role of the Ki-67 index[2,3].Metastatic Type 1 g-NETs are rare and treatment of advanced cases mirrors that of other advanced NETs,including somatostatin analogs(SSA)and peptide receptor radionuclide therapy(PRRT),though specific data are limited[1].
关 键 词:ELLISON NEUROENDOCRINE GASTRIC
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