Risk of breast cancer in Lynch syndrome: a systematic review

AK Win, NM Lindor, MA Jenkins - Breast Cancer Research, 2013 - Springer
Introduction Lynch syndrome is an autosomal dominantly inherited disorder of cancer
susceptibility caused by germline mutations in the DNA mismatch repair (MMR) genes …

Mismatch repair status and clinical outcome in endometrial cancer: a systematic review and meta-analysis

I Diaz-Padilla, N Romero, E Amir, X Matias-Guiu… - Critical reviews in …, 2013 - Elsevier
Background The association between the deficiency in mismatch repair (MMR) genes and
prognosis in women with endometrial cancer is unclear. Here we report a systematic review …

Familial risk-colorectal cancer: ESMO clinical practice guidelines

J Balmaña, F Balaguer, A Cervantes… - Annals of …, 2013 - annalsofoncology.org
Lynch syndrome is the most common hereditary colorectal cancer (CRC) syndrome and it
accounts for∼ 1%-3% of all CRC burden [1]. The syndrome is transmitted with an autosomal …

Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention

KH Lu, M Daniels - Familial cancer, 2013 - Springer
Women with Lynch syndrome have an additional need to address the substantial increased
lifetime risk of endometrial and ovarian cancer. Endometrial or ovarian cancer can be the …

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers

AK Win, S Parry, B Parry, MF Kalady, FA Macrae… - Annals of surgical …, 2013 - Springer
Background Despite regular surveillance colonoscopy, the metachronous colorectal cancer
risk for mismatch repair (MMR) gene mutation carriers after segmental resection for colon …

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

AK Win, NM Lindor, I Winship, KM Tucker… - JNCI: Journal of the …, 2013 - academic.oup.com
Background Lynch syndrome is an autosomal dominantly inherited disorder caused by
germline mutations in DNA mismatch repair (MMR) genes. Previous studies have shown …

BRAF mutation in sporadic colorectal cancer and Lynch syndrome

A Thiel, M Heinonen, J Kantonen, A Gylling, L Lahtinen… - Virchows Archiv, 2013 - Springer
The aim of the study was to detect mutations of BRAF oncogene in colorectal cancer and to
use this information to identify Lynch syndrome patients. Consecutive cases of primary …

Colorectal cancer screening

RW Burt, JA Cannon, DS David, DS Early… - Journal of the National …, 2013 - jnccn.org
Mortality from colorectal cancer can be reduced by early diagnosis and by cancer prevention
through polypectomy. These NCCN Guidelines for Colorectal Cancer Screening describe …

Lynch syndrome-associated neoplasms: a discussion on histopathology and immunohistochemistry

J Shia, S Holck, G DePetris, JK Greenson, DS Klimstra - Familial Cancer, 2013 - Springer
It was a century ago that Warthin, a pathologist, first described the clinical condition now
known as Lynch syndrome. One hundred years later, our understanding of this syndrome …

How do we approach the goal of identifying everybody with Lynch syndrome?

H Hampel, A De La Chapelle - Familial cancer, 2013 - Springer
Lynch syndrome (LS) is the most common inherited cause of colorectal (CRC) and
endometrial cancer. We here define LS as an individual with a germline deleterious …