Intraductal papillary mucinous neoplasm of the pancreas in a patient with attenuated familial adenomatous polyposis

被引:38
作者
Chetty, R
Salahshor, S
Bapat, B
Berk, T
Croitoru, M
Gallinger, S
机构
[1] Princess Margaret Hosp, Univ Hlth Network, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Pathol, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Familial GI Canc Registry, Toronto, ON M5G 1X5, Canada
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Ctr Canc Genet, Toronto, ON M5G 1X5, Canada
[5] Ontario Canc Inst, Dept Med Biophys, Toronto, ON, Canada
[6] Univ Toronto, Dept Surg, Toronto, ON, Canada
关键词
D O I
10.1136/jcp.2004.020925
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A 67 year old man with a clinical diagnosis of attenuated familial adenomatous polyposis ( AFAP) and a past history of synchronous colon cancers in the transverse colon was also found to have an intraductal papillary mucinous neoplasm (IPMN) of the pancreas. In addition, several foci of heterotopic gastric oxyntic mucosa were noted in the duodenum, interspersed with flat and polypoid adenomas. The duodenal adenomas showed low grade dysplasia, loss of adenomatous polyposis coli (APC) protein expression, but retention of beta catenin staining, localised to the nucleus and cytoplasm. The IPMN in the pancreas showed an identical immunohistochemical profile to the duodenal adenomas. The heterotopic gastric foci in the duodenum were negative for the APC protein, and b catenin staining was membranous in location. Although the patient did not show germline truncating APC mutations or mutations in the MYH gene, the past history, clinical features, and immunohistochemical profile of the various lesions suggest strongly that the IPMN is part of the spectrum of lesions encountered in AFAP. Whether the heterotopic oxyntic gastric mucosa in the duodenum is also related is unclear, but it may represent a forme fruste of fundic gland polyps.
引用
收藏
页码:97 / 101
页数:5
相关论文
共 31 条
  • [1] Sporadic fundic gland polyps -: Common gastric polyps arising through activating mutations in the β-catenin gene
    Abraham, SC
    Nobukawa, B
    Giardiello, FM
    Hamilton, SR
    Wu, TT
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03) : 1005 - 1010
  • [2] Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
    Al-Tassan, N
    Chmiel, NH
    Maynard, J
    Fleming, N
    Livingston, AL
    Williams, GT
    Hodges, AK
    Davies, DR
    David, SS
    Sampson, JR
    Cheadle, JR
    [J]. NATURE GENETICS, 2002, 30 (02) : 227 - 232
  • [3] Reciprocity between membranous and nuclear expression of beta-catenin in colorectal tumours
    Hao, XP
    Tomlinson, I
    Ilyas, M
    Palazzo, JP
    Talbot, IC
    [J]. VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 1997, 431 (03): : 167 - 172
  • [4] Immunohistochemical evaluation of adenomatous polyposis coli, β-catenin, c-Myc, cyclin D1, p53, and retinoblastoma protein expression in syndromic and sporadic fundic gland polyps
    Hassan, A
    Yerian, LM
    Kuan, SF
    Xiao, SY
    Hart, J
    Wang, HLL
    [J]. HUMAN PATHOLOGY, 2004, 35 (03) : 328 - 334
  • [5] Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status
    Heinimann, K
    Müllhaupt, B
    Weber, W
    Attenhofer, M
    Scott, RJ
    Fried, M
    Martinoli, S
    Müller, HJ
    Dobbie, Z
    [J]. GUT, 1998, 43 (05) : 675 - 679
  • [6] Hernegger GS, 2002, DIS COLON RECTUM, V45, P127
  • [7] Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations
    Jones, S
    Emmerson, P
    Maynard, J
    Best, JM
    Jordan, S
    Williams, GT
    Sampson, JR
    Cheadle, JP
    [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (23) : 2961 - 2967
  • [8] KLIMSTRA DS, 2004, MODERN PATHOL, V17, pA305
  • [9] Attenuated familial adenomatous polyposis (AFAP). A review of the literature
    Anne Lyster Knudsen
    Marie Luise Bisgaard
    Steffen Bülow
    [J]. Familial Cancer, 2003, 2 (1) : 43 - 55
  • [10] Le Borgne J, 1997, Chirurgie, V122, P31