Langer Peter, Slater Emily, Fendrich Volker, Habbe Nils, Bartsch Detlef K
Philipps-University Hospital, Department of General Surgery, Baldingerstraße, D-35043 Marburg, Germany +49 6421 2866442 ; +49 6421 2868995
Expert Opin Med Diagn. 2007 Oct;1(2):193-201. doi: 10.1517/17530059.1.2.193.
The term 'familial pancreatic cancer (FPC) defines families with at least two first-degree relatives with confirmed pancreatic cancer that do not fulfill the criteria of other inherited cancer syndromes with an increased risk for the development of PC, such as Peutz-Jeghers syndrome, hereditary pancreatitis and hereditary breast and ovarian cancer. FPC is a mostly autosomal dominant inherited tumor syndrome with a heterogeneous phenotype. The major genetic defect has not been identified yet, although mutations, for example in the BRCA2 gene, could be identified in some FPC families. Nevertheless, most experts recommend participation in screening and surveillance programs to high-risk individuals. Most board-approved screening programs are based on endoscopic ultrasound. The first data on the prospective screening of high-risk individuals have demonstrated that precursor lesions of PC can be identified, but false-positive findings do occur.
术语“家族性胰腺癌(FPC)”指的是至少有两名一级亲属确诊患有胰腺癌,且不符合其他遗传性癌症综合征(如黑斑息肉综合征、遗传性胰腺炎以及遗传性乳腺癌和卵巢癌,这些综合征会增加患胰腺癌的风险)标准的家族。FPC是一种大多呈常染色体显性遗传的肿瘤综合征,具有异质性表型。尽管在一些FPC家族中可检测到例如BRCA2基因的突变,但主要的基因缺陷尚未明确。然而,大多数专家建议高危个体参与筛查和监测项目。多数经委员会批准的筛查项目基于内镜超声检查。关于高危个体前瞻性筛查的首批数据表明,胰腺癌的前驱病变能够被识别出来,但假阳性结果确实存在。