Metachronous Colorectal Cancer in Icelandic MSH6 and PMS2 Lynch Syndrome Carriers in 1955-2017: A Population-based Study

被引:2
|
作者
Andresdottir, Arna Kristin [1 ]
Einarsson, Haukur [2 ,3 ]
Jonsdottir, Hildur [1 ]
Jonasson, Jon Gunnlaugur [2 ,4 ]
Bjornsson, Einar Stefan [1 ,4 ]
Haraldsdottir, Sigurdis [1 ,2 ,4 ,5 ,6 ]
机构
[1] Landspitali Univ Hosp Iceland, Dept Med, Reykjavik, Iceland
[2] Landspitali Univ Hosp Iceland, Dept Pathol, Reykjavik, Iceland
[3] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[4] Univ Iceland, Fac Med, Reykjavik, Iceland
[5] Landspitali Univ Hosp Iceland, Dept Oncol, Reykjavik, Iceland
[6] Landspitali Univ Hosp, Dept Oncol, IS-101 Reykjavik, Iceland
关键词
COLECTOMY; RISK;
D O I
10.1053/j.gastro.2023.02.007
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
引用
下载
收藏
页数:4
相关论文
共 46 条
  • [21] Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012
    Rahner, Nils
    Steinke, Verena
    Schlegelberger, Brigitte
    Eisinger, Francois
    Hutter, Pierre
    Olschwang, Sylviane
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2013, 21 (01) : 118 - 118
  • [22] Germline mutation and protein expression analysis of mismatch repair genes MSH6 and PMS2 in Malaysian Lynch syndrome patients
    Zahary, Mohd Nizam
    Kaur, Gurjeet
    Abu Hassan, Muhammad Radzi
    Sidek, Ahmad Shanwani Mohd
    Singh, Harjinder
    Yeh, Lee Yeong
    Ankathil, Ravindran
    INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2014, 29 (02) : 261 - 262
  • [23] Germline mutation and protein expression analysis of mismatch repair genes MSH6 and PMS2 in Malaysian Lynch syndrome patients
    Mohd Nizam Zahary
    Gurjeet Kaur
    Muhammad Radzi Abu Hassan
    Ahmad Shanwani Mohd Sidek
    Harjinder Singh
    Lee Yeong Yeh
    Ravindran Ankathil
    International Journal of Colorectal Disease, 2014, 29 : 261 - 262
  • [24] Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population
    Pratibha Bhai
    Samarth Kulshrestha
    Ratna D. Puri
    Sunita Bijarnia Mahay
    Renu Saxena
    Ishwar Chander Verma
    Indian Journal of Gastroenterology, 2020, 39 : 599 - 607
  • [25] Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population
    Bhai, Pratibha
    Kulshrestha, Samarth
    Puri, Ratna D.
    Bijarnia Mahay, Sunita
    Saxena, Renu
    Verma, Ishwar Chander
    INDIAN JOURNAL OF GASTROENTEROLOGY, 2020, 39 (06) : 599 - 607
  • [26] Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide study
    Boumehdi, Asma-Lamia
    Cherbal, Farid
    Khider, Feriel
    Oukkal, Mohammed
    Mahfouf, Hassen
    Zebboudj, Ferhat
    Maaoui, Mustapha
    ANNALS OF HUMAN GENETICS, 2022, 86 (06) : 328 - 352
  • [27] ENDOMETRIAL ADENOCARCINOMA IN PATIENTS WITH LYNCH SYNDROME: IMMUNOHISTOCHEMISTRY FOR P53 PROTEIN AND MLH1, MSH2, MSH6 AND PMS2 PROTEINS
    Pessini, S.
    Zettler, C. G.
    Ashton-Prolla, P.
    Cossio, S. L.
    Meurer, L.
    Pellanda, L. C.
    Silveira, G. P. G.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2013, 23 (08)
  • [28] Early age of onset and broad cancer spectrum persist in MSH6 and PMS2-associated Lynch syndrome.
    Liu, Ying L.
    Cadoo, Karen Anne
    Maio, Anna
    Patel, Zalak
    Kemel, Yelena
    Salo-Mullen, Erin E.
    Catchings, Amanda
    Ranganathan, Megha
    Kane, Sarah R.
    Shia, Jinru
    Soslow, Robert A.
    Birsoy, Ozge
    Mandelker, Diana
    Hechtman, Jaclyn Frances
    Carlo, Maria Isabel
    Walsh, Michael Francis
    Markowitz, Arnold
    Offit, Kenneth
    Stadler, Zsofia Kinga
    Latham, Alicia
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)
  • [29] Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary Nonpolyposis colorectal cancer (HNPCC)
    van der Klift, H
    Wijnen, J
    Wagner, A
    Verkuilen, P
    Tops, C
    Otway, R
    Kohonen-Corish, M
    Vasen, H
    Oliani, C
    Barana, D
    Moller, P
    DeLozier-Blanchet, C
    Hutter, P
    Foulkes, W
    Lynch, H
    Burn, J
    Möslein, G
    Fodde, R
    GENES CHROMOSOMES & CANCER, 2005, 44 (02): : 123 - 138
  • [30] Implementation of Universal Colorectal Cancer Screening for Lynch Syndrome: A Population-Based Study
    Sierra, Isabel
    Diaz-Algorri, Yaritza
    Maldonado, Valerie
    Alicea, Kimberly
    Rosado, Kathia
    Cruz-Correa, Marcia
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2017, 26 (02)