Literature DB >> 7979199

The tumor spectrum in HNPCC.

P Watson1, H T Lynch.   

Abstract

HNPCC is an inherited disorder characterized by an increased risk for cancers of the colorectum and endometrium. An increased risk of cancer of other organs, and heterogeneity among HNPCC families in extracolonic cancer risk, has been hypothesized. We evaluated these hypotheses in a study of 1317 high risk members of 23 HNPCC families. Expected numbers of cancer occurrences were calculated from general population incidence data, and compared to observed numbers. The distribution of cancers among families was compared to the distribution expected under the hypothesis of uniform risk. Significant excesses of cancers of the stomach, small bowel, hepatobiliary system, upper urologic tract, and ovary were found. Gastrointestinal tract cancers were uniformly distributed among families, but urologic tract and gynecologic tract cancers were significantly heterogeneously distributed. Our results indicate that HNPCC family members are at increased risk for cancer at specific extracolonic sites. We also found evidence of heterogeneity among HNPCC families in the risk for some extracolonic cancers.

Entities:  

Mesh:

Year:  1994        PMID: 7979199

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  33 in total

1.  Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.

Authors:  Kandelaria Rumilla; Karen V Schowalter; Noralane M Lindor; Brittany C Thomas; Kara A Mensink; Steven Gallinger; Spring Holter; Polly A Newcomb; John D Potter; Mark A Jenkins; John L Hopper; Tiffany I Long; Daniel J Weisenberger; Robert W Haile; Graham Casey; Peter W Laird; Loic Le Marchand; Stephen N Thibodeau
Journal:  J Mol Diagn       Date:  2010-12-23       Impact factor: 5.568

2.  Approach to early-onset colorectal cancer: clinicopathological, familial, molecular and immunohistochemical characteristics.

Authors:  Jose Perea; Edurne Alvaro; Yolanda Rodríguez; Cristina Gravalos; Eva Sánchez-Tomé; Barbara Rivera; Francisco Colina; Pablo Carbonell; Rogelio González-Sarmiento; Manuel Hidalgo; Miguel Urioste
Journal:  World J Gastroenterol       Date:  2010-08-07       Impact factor: 5.742

3.  Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank.

Authors:  Rachel E Rosenblum; Celina Ang; Sabrina A Suckiel; Emily R Soper; Meenakshi R Sigireddi; Sinead Cullina; Gillian M Belbin; Aimee L Lucas; Eimear E Kenny; Noura S Abul-Husn
Journal:  JCO Precis Oncol       Date:  2020-11-23

Review 4.  Importance of PCR-based Tumor Testing in the Evaluation of Lynch Syndrome-associated Endometrial Cancer.

Authors:  Amanda S Bruegl; Annessa Kernberg; Russell R Broaddus
Journal:  Adv Anat Pathol       Date:  2017-11       Impact factor: 3.875

Review 5.  Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.

Authors:  Henry T Lynch; Stephen Lanspa; Trudy Shaw; Murray Joseph Casey; Marc Rendell; Mark Stacey; Theresa Townley; Carrie Snyder; Megan Hitchins; Joan Bailey-Wilson
Journal:  Fam Cancer       Date:  2018-07       Impact factor: 2.375

6.  Urothelial carcinoma in a man with hereditary nonpolyposis colon cancer.

Authors:  Dean L Lenz; Lewis E Harpster
Journal:  Rev Urol       Date:  2003

7.  Clinicopathological and molecular genetic analysis of HNPCC in China.

Authors:  Ding-Cun Luo; Qi Cai; Meng-Hong Sun; Yao-Zhong Ni; Shi-Chang Ni; Zhe-Jing Chen; Xiao-Yang Li; Chong-Wei Tao; Xue-Miao Zhang; Da-Ren Shi
Journal:  World J Gastroenterol       Date:  2005-03-21       Impact factor: 5.742

Review 8.  Colorectal cancer molecular profiling: from IHC to NGS in search of optimal algorithm.

Authors:  Larissa V Furtado; Wade S Samowitz
Journal:  Virchows Arch       Date:  2017-05-27       Impact factor: 4.064

Review 9.  Impact of DNA mismatch repair system alterations on human fertility and related treatments.

Authors:  Min-hao Hu; Shu-yuan Liu; Ning Wang; Yan Wu; Fan Jin
Journal:  J Zhejiang Univ Sci B       Date:  2016-01       Impact factor: 3.066

Review 10.  Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

Authors:  Katharina Wimmer; Julia Etzler
Journal:  Hum Genet       Date:  2008-08-18       Impact factor: 4.132

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