A Case of Pancreatic Neuroendocrine Tumor Mimicked Intraductal Papillary Mucinous Neoplasm
作者： Sung Birm Sohn , Hyo Jung Kim , Jae Seon Kim , Baek Hui Kim , Sang Hun Kim
DOI: 10.15279/KPBA.2014.19.4.210
关键词: Neuroendocrine tumors 、 Pancreas 、 Male patient 、 General surgery 、 Medicine 、 Pancreatic duct 、 Pathology 、 Intraductal papillary mucinous neoplasm 、 Lesion 、 Pancreatic neuroendocrine tumor
摘要: Neuroendocrine tumors of the pancreas are exremely rare tumors, but recent imaging examination advances, diagnostic frequency is also increasing. However, there difficulty diagnosis pancreatic serotonin producing neuroendocrine because grow slowly and clinical symptoms not significant. A 60-year-old male patient with duct dilatation progresses gradually during seven years without obstructing lesion in studies, we suspected mass as intraductal papillary mucinous neoplasm. diagnosed his case tumor after surgery report here literature review. Korean J Pancreatobiliary 2014;19(4):210-214
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