血管活性肠肽瘤1例  

Pancreatic vasoactive intestinal polypeptidesecreting tumor:A case report

作　　者：张丽平[1] 吴会超[1] 罗兰[1] 

机构地区：[1]遵义医学院附属医院消化内科,贵州省遵义市563099

出　　处：《世界华人消化杂志》2013年第21期2117-2120,共4页World Chinese Journal of Digestology

基　　金：贵州省科技厅社会攻关计划基金资助项目;No.SY[2010]3085~~

摘　　要：血管活性肠肽瘤(vasoactive-intestinal polypeptidesecreting tumors,VIPomas)是罕见的胰腺内分泌肿瘤.临床上以大量水样腹泻,顽固性低血钾,胃酸缺乏为主要特征性表现.此病非常罕见,临床上较易误诊.本文报道血管活性肠肽瘤1例,通过病史及实验室、影像学、内镜学、组织学检查结合相关文献进行分析讨论,提高对该病的认识.Vasoactive intestinal polypeptide-secreting tu- mor （VIPoma） of the pancreas is a rare type of pancreatic endocrine neoplasm. The main clini- cal features of VIPoma include large amount of watery diarrhea, hypokalemia and achlorhydria. Due to extreme rarity of this disease, it is eas- ily misdiagnosed. Here we report such a case to raise the awareness of this clinical entity. We also performed a review of the literature to sum- marize its clinical manifestations, diagnosis and treatment.

关 键 词：血管活性肠肽瘤 水样腹泻 低钾血症 诊断 

分 类 号：R735.9[医药卫生—肿瘤]