Characteristics of early-onset vs late-onset colorectal cancer: a review

R Collaborative, AM Zaborowski, A Abdile… - JAMA …, 2021 - jamanetwork.com
Importance The incidence of early-onset colorectal cancer (younger than 50 years) is rising
globally, the reasons for which are unclear. It appears to represent a unique disease …

[HTML][HTML] The management of Peutz–Jeghers syndrome: European hereditary tumour group (EHTG) guideline

A Wagner, S Aretz, A Auranen, MJ Bruno… - Journal of clinical …, 2021 - mdpi.com
The scientific data to guide the management of Peutz–Jeghers syndrome (PJS) are sparse.
The available evidence has been reviewed and discussed by diverse medical specialists in …

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

N Hearle, V Schumacher, FH Menko, S Olschwang… - Clinical Cancer …, 2006 - AACR
Background: Although an increased cancer risk in Peutz-Jeghers syndrome is established,
data on the spectrum of tumors associated with the disease and the influence of germ-line …

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

HFA Vasen, I Blanco, K Aktan-Collan, JP Gopie… - Gut, 2013 - gut.bmj.com
Lynch syndrome (LS) is characterised by the development of colorectal cancer, endometrial
cancer and various other cancers, and is caused by a mutation in one of the mismatch repair …

The “unnatural” history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance

A Ahadova, TT Seppälä, C Engel… - … journal of cancer, 2021 - Wiley Online Library
Individuals with Lynch syndrome (LS), one of the most common inherited cancer syndromes,
are at increased risk of developing malignancies, in particular colorectal cancer (CRC) …

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome …

P Møller, T Seppälä, I Bernstein, E Holinski-Feder… - Gut, 2017 - gut.bmj.com
Objective Estimates of cancer risk and the effects of surveillance in Lynch syndrome have
been subject to bias, partly through reliance on retrospective studies. We sought to establish …

[HTML][HTML] Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

M Dominguez-Valentin, JR Sampson, TT Seppälä… - Genetics in …, 2020 - nature.com
Purpose Pathogenic variants affecting MLH1, MSH2, MSH6, and PMS2 cause Lynch
syndrome and result in different but imprecisely known cancer risks. This study aimed to …

Familial endometrial cancer in female carriers of MSH6 germline mutations

J Wijnen, W Leeuw, H Vasen, H Klift, P Møller… - Nature …, 1999 - nature.com
MSH6 germline mutations 142 nature genetics• volume 23• october 1999 gressive muscular
dystrophy. This mouse will become a useful animal model for studying the …

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444

R Caspari, S Olschwang, W Friedl… - Human Molecular …, 1995 - academic.oup.com
An earlier study has shown that FAP patients with mutations in codons 136–302 of the APC
gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE) …

[HTML][HTML] Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

J Burn, DT Bishop, JP Mecklin, F Macrae… - … England Journal of …, 2008 - Mass Medical Soc
Background Observational and epidemiologic data indicate that the use of aspirin reduces
the risk of colorectal neoplasia; however, the effects of aspirin in the Lynch syndrome …