Hereditary intraductal papillary mucinous neoplasm of the pancreas

被引:7
|
作者
Denost, Q. [1 ]
Chafai, N. [1 ]
Arrive, L. [2 ]
Mourra, N. [3 ]
Paye, F. [1 ]
机构
[1] Hop St Antoine, Dept Digest Surg, F-75012 Paris, France
[2] Hop St Antoine, Dept Radiol, F-75571 Paris, France
[3] Hop St Antoine, Dept Pathol, F-75571 Paris, France
关键词
CLINICOPATHOLOGICAL FEATURES; TUMORS; MALIGNANCY; RECURRENCE; PATIENT;
D O I
10.1016/j.clinre.2011.11.013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Intraductal papillary mucinous neoplasm (IPMN) is a rare pancreatic tumor defined as intraductal mucin-producting neoplasm with tall, columnar, mucin-containing epithelium. IPMN have already been described in association with inherited genetic disorder including familial adenomatous polyposis and Peutz-Jeghers syndrome. However, there is no reported description of familial history of IPMN. We reported in this case-report IPMN in the first-degree relatives without familial history of colorectal polyposis or previous extra-pancreatic cancer. The rarety of IPMN suggests that the coexistence of this tumor in two first-degree relatives is probably due to a genetic inherited factor that remains to be elucidated. (c) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:E23 / E25
页数:3
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