Recurrent idiopathic pancreatitis in familial adenomatous polyposis: Report of a case-series and review of the literature

被引:5
|
作者
van Esch, Aura A. J. [1 ]
Drenth, Joost P. H. [1 ]
Morsche, Rene H. M. te [1 ]
Jansen, Jan B. M. J. [1 ]
Nagengast, Fokko M. [1 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Gastroenterol & Hepatol, NL-6500 HB Nijmegen, Netherlands
关键词
familial adenomatous polyposis; pancreatitis; SPINK1;
D O I
10.1007/s10689-007-9118-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Familial adenomatous polyposis (FAP) is characterized by the development of multiple adenomatous polyps predominantly in the colon but also in the duodenum. Scattered case reports indicate that there is a risk for pancreatitis in FAR The most likely cause of pancreatitis in FAP is obstructing ampullary adenomas. We describe 7 FAP patients who experienced one or more episodes of pancreatitis. Two patients experienced pancreatitis after endoscopic treatment of ampullary adenoma. The cause of the pancreatitis in 5 of 7 patients could not be determined, as none of the patients had obstruction of the ampulla. Furthermore, other risk factors for pancreatitis such as pancreatic serine protease inhibitor Kazal type I (SPINK1) gene mutations were ruled out. A review of literature identified 20 FAP patients who developed the first episode of pancreatitis at a mean age of 45 years (range 23-72 years). Some 55% had recurrent episodes of pancreatitis. Eight patients had (peri) ampullary adenomas or carcinomas. In most cases, the course of pancreatitis was mild with an uneventful outcome, but one patient died after an episode of acute pancreatitis.
引用
收藏
页码:275 / 280
页数:6
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