نتایج جستجو برای: lynch syndrome

تعداد نتایج: 623651  

2017
Min Kyu Kim

After the discovery of Lynch syndrome in the 1960s [1], its definition started from hereditary nonpolyposis colorectal cancer (HNPCC) specifically focusing affected organs. However, affected organs include nearly the whole body the endometrium, ovary, ureter, stomach, pancreas, biliary system, small bowel, brain, and skin. The past several decades have shifted our focus from organs to genes. In...

2012
Bente A Talseth-Palmer Juul T Wijnen Ingvild S Brenne Shantie Jagmohan-Changur Katie A Ashton Carli M Tops Tiffany-Jane Evans Mary McPhillips Claire Groombridge Janina Suchy Grzegorz Kurzawski Allan Spigelman Pål Møller Hans M Morreau Tom Van Wezel Jan Lubinski Hans FA Vasen Rodney J Scott

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts Bente A Talseth-Palmer, Juul T Wijnen, Ingvild S Brenne, Shantie Jagmohan-Changur, Katie A Ashton, Carli M Tops, Tiffany-Jane Evans, Mary McPhillips, Claire Groombridge, Janina Suchy, Grzegorz Kurzawski, The Dutch Cancer G...

2012
KENTA MASUDA KOUJI BANNO AKIRA HIRASAWA MEGUMI YANOKURA KOSUKE TSUJI YUSUKE KOBAYASHI IORI KISU ARISA UEKI HIROYUKI NOMURA EIICHIRO TOMINAGA NOBUYUKI SUSUMU DAISUKE AOKI

Lynch syndrome is a genetic disease that often develops in patients with endometrial cancer and is caused by abnormal DNA mismatch repair (MMR) genes. In the United States, it was recently reported that the prevalence of Lynch syndrome with an hMSH2 mutation in patients with endometrial cancer in the lower uterine segment (LUS) is much greater tha...

Journal: :Oncology 2005
Henry T Lynch Jane F Lynch

The Lynch syndrome (hereditary nonpolyposis colorectal cancer [HNPCC]), is the most common form of hereditary colorectal cancer (CRC), accounting for 2% to 7% of all CRC cases. The next most common hereditary CRC syndrome is familial adenomatous polyposis (FAP), which accounts for less than 1% of all CRC. Lynch syndrome is of crucial clinical importance due to the fact that it predicts the life...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2013
Robyn L Ward Sian Hicks Nicholas J Hawkins

PURPOSE Molecular screening techniques are available to identify hereditary Lynch syndrome in people with newly diagnosed colorectal cancer (CRC). We aimed to determine whether decisions of patients or clinicians reduced detection of Lynch syndrome. PATIENTS AND METHODS A prospective cohort of 245 consecutive individuals with mismatch repair-deficient CRC recruited from a population-based mol...

Journal: :Anticancer research 2014
Anne-Sophie Bats Helene Blons Celine Narjoz Marie-Aude Le Frere-Belda Pierre Laurent-Puig Fabrice Lecuru

AIM To assess the feasibility of Microsatellite Instability (MSI) analysis in uterine cavity washings for detecting endometrial cancer in Lynch syndrome. MATERIALS AND METHODS This was a proof-of-concept study in Lynch syndrome patients, scheduled for hysterectomy. At the beginning of surgical procedure, uterine cavity washings were performed, and sent for MSI analysis. Pathological examinati...

2016
Melissa K Frey Gizelka David-West Khushbakhat R Mittal Franco M Muggia Bhavana Pothuri

Occult endometrial cancer is occasionally discovered in women with Lynch syndrome undergoing risk-reducing hysterectomy. The case presented here demonstrates that preoperative endometrial sampling can help detect these occult cancers; however, there are currently no recommendations for this preoperative intervention. A 50-year-old woman with Lynch syndrome underwent endometrial sampling prior t...

2014
Yen Y. Tan Lisa J. Fitzgerald

This article explores the views of general practitioners and specialists on their referral of patients with suspected Lynch syndrome to cancer genetic services. Using a purposive maximum variation sampling strategy, we conducted semi-structured interviews face-to-face with 28 general practitioners and specialists in public or private hospitals and specialist clinics between March and August 201...

2014
Ralph Schneider Claudia Schneider Christian Jakobeit Alois Fürst Gabriela Möslein

BACKGROUND The most frequent hereditary colorectal cancer (CRC) syndromes are Lynch syndrome and familial adenomatous polyposis (FAP), accounting for approximately 5% of the CRC burden. Both are characterized by an autosomal dominant mode of transmission and require an individualized approach of intensified screening and prophylactic surgery. METHODS In this review, we provide an overview of ...

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