Attenuated familial adenomatous polyposis with desmoids caused by an APC mutation

被引:5
|
作者
Tsuneo Ikenoue
Kiyoshi Yamaguchi
Mitsuhiro Komura
Seiya Imoto
Rui Yamaguchi
Eigo Shimizu
Shinichi Kasuya
Tetsuo Shibuya
Seira Hatakeyama
Satoru Miyano
Yoichi Furukawa
机构
[1] Advanced Clinical Research Center,Division of Clinical Genome Research
[2] The Institute of Medical Science,undefined
[3] The University of Tokyo,undefined
[4] Laboratory of DNA Information Analysis,undefined
[5] Human Genome Center,undefined
[6] The Institute of Medical Science,undefined
[7] The University of Tokyo,undefined
[8] Laboratory of Sequence Analysis,undefined
[9] Human Genome Center,undefined
[10] The Institute of Medical Science,undefined
[11] The University of Tokyo,undefined
关键词
D O I
10.1038/hgv.2015.11
中图分类号
学科分类号
摘要
We present here a case of attenuated familial adenomatous polyposis (AFAP) with a family history of desmoids and thyroid tumors. This patient had no colonic polyps but did have multiple desmoids. Genetic analysis identified a 4-bp deletion in codon 2644 (c.7932_7935delTTAT: p.Tyr2645LysfsX14) of the adenomatous polyposis coli (APC) gene. In cases with limited numbers of colonic polyps and desmoids, AFAP may be caused by a mutation in the 3′ region of APC.
引用
收藏
相关论文
共 50 条
  • [41] Treatment of desmoids and mesenteric fibromatosis in familial adenomatous polyposis with raloxifene
    Tonelli, F
    Ficari, F
    Valanzano, R
    Brandi, ML
    [J]. TUMORI JOURNAL, 2003, 89 (04): : 391 - 396
  • [42] Telomere length in familial adenomatous polyposis-associated desmoids
    Middleton, SB
    Pack, K
    Phillips, RKS
    [J]. DISEASES OF THE COLON & RECTUM, 2000, 43 (11) : 1535 - 1539
  • [43] Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis
    Nielsen, M.
    Hes, F. J.
    Nagengast, F. M.
    Weiss, M. M.
    Mathus-Vliegen, E. M.
    Morreau, H.
    Breuning, M. H.
    Wijnen, J. T.
    Tops, C. M. J.
    Vasen, H. F. A.
    [J]. CLINICAL GENETICS, 2007, 71 (05) : 427 - 433
  • [44] APC intragenic haplotypes in familial adenomatous polyposis
    Almeida, R
    Morton, N
    Fidalgo, P
    Leitao, N
    Mira, C
    Rueff, J
    Monteiro, C
    [J]. CLINICAL GENETICS, 1996, 50 (06) : 483 - 485
  • [45] Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene
    Brensinger, JD
    Laken, SJ
    Luce, MC
    Powell, SM
    Vance, GH
    Ahnen, DJ
    Petersen, GM
    Hamilton, SR
    Giardiello, FM
    [J]. GUT, 1998, 43 (04) : 548 - 552
  • [46] 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
  • [47] Identification a nonsense mutation of APC gene in Chinese patients with familial adenomatous polyposis
    Li, Haishan
    Zhang, Lingling
    Jiang, Quan
    Shi, Zhenwang
    Tong, Hanxing
    [J]. EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2017, 13 (04) : 1495 - 1499
  • [48] Erythromycin readthrough of APC nonsense stop codon mutation in Familial adenomatous polyposis
    Kariv, R.
    Fliss-Isacov, N.
    Caspi, M.
    Arbesfeld, R.
    [J]. ANNALS OF ONCOLOGY, 2018, 29
  • [49] Somatic mutation of the APC gene in thyroid carcinoma associated with familial adenomatous polyposis
    Iwama, T
    Konishi, M
    Iijima, T
    Yoshinaga, K
    Tominaga, T
    Koike, M
    Miyaki, M
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 1999, 90 (04): : 372 - 376
  • [50] Serrated adenoma in familial adenomatous polyposis: relation to germline APC gene mutation
    Matsumoto, T
    Iida, M
    Kobori, Y
    Mizuno, M
    Nakamura, S
    Hizawa, K
    Yao, T
    [J]. GUT, 2002, 50 (03) : 402 - 404