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췌관내 유두상 점액종양으로 오인된 췌장의 신경내분비종양
손성범 ( Sung Birm Sohn ),김효정 ( Hyo Jung Kim ),김재선 ( Jae Seon Kim ),김백희 ( Baek Hui Kim ),김상훈 ( Sang Hun Kim ),김지형 ( Ji Hyoung Kim ),송지영 ( Ji Young Song ),김태현 ( Tae Hyun Kim ) 대한췌장담도학회 2014 대한췌담도학회지 Vol.19 No.4
Neuroendocrine tumors of the pancreas are exremely rare tumors, but recent imaging examination advances, diagnostic frequency is also increasing. However, there is difficulty of diagnosis of pancreatic serotonin producing neuroendocrine tumors, because tumors grow slowly and clinical symptoms are not significant. A 60-year-old male patient with pancreatic duct dilatation progresses gradually during the seven years without obstructing lesion in imaging studies, we suspected the mass as intraductal papillary mucinous neoplasm. However, we diagnosed his case as neuroendocrine tumor after surgery and report here with literature review. Korean J Pancreatobiliary 2014;19(4):210-214