Hereditary Colorectal Cancer

ISBN-13: 9781441966025 / Angielski / Twarda / 2010 / 630 str.

M. a. Rodriguez-Bigas; Miguel A. Rodriguez-Bigas; Raul Cutait

Opis

Colorectal cancer is the third most commonly diagnosed cancer in the US and the third most recently linked to cancer deaths. The national annual incidence rate of colorectal cancer is approximately 148,000+, striking slightly more females than males. The lifetime risk of colorectal cancer is 5-6%, however patients with a familial risk (with two or more first or second degree relatives) make up 20% of the patients. Persons who carry genetic mutations linked to hereditary colorectal cancer are the most likely to develop the disease.

Recenzje

"This unique book is designed as a consultative source for individuals involved in the care of patients with colorectal cancer and patients at risk due to familial genetic testing. ... Genetics counselors, medical geneticists, surgeons, and oncology specialists would find this book extremely useful. ... The intimidating subject of hereditary colorectal cancer is well reviewed and presented in an easy-to-read manner. A job well done." (Luis F. Escobar, Doody's Book Reviews, October, 2018)

"This comprehensive book details basic scientific knowledge, clinically relevant algorithms, and the historical framework of hereditary colorectal cancer. ... It is written for colorectal specialists, which may include surgeons, gastroenterologists, oncologists, and geneticists. ... The book would be an excellent definitive reference for any medical library. ... There is no comparable book, and the information it provides would be very difficult to obtain from other sources in such a well - balanced and complete presentation." (Neal Wilkinson, Doody's Review Service, January, 2011)

Spis treści

Introduction.- Familial Adenomatous Polyposis.- Historical Aspects of Lynch Syndrome.- Molecular Genetics of Familial Adenomatous Polyposis.- DNA Mismatch Repair.- Hamartomatous Polyposis.- Hyperplastic Polyposis Syndrome: Colorectal Cancer Predisposition.- MUTYH-Associated Polyposis.- Polymorphic Variation and Risk of Colorectal Cancer.- The Pathologist and the Phenotype of Hereditary Colorectal Cancer.- Genotype Phenotype Correlation in Familial Adenomatous Polyposis (FAP).- Surgery for Familial Adenomatous Polyposis.- Duodenal Adenomas in Familial Adenomatous Polyposis.- FAP Associated Desmoid Tumours.- Attenuated Familial Adenomatous Polyposis: Diagnosis, Management and Future Prognosis.- An Overview of the Lynch Syndrome (hereditary nonpolyposis colorectal cancer, HNPCC).- Surgical Management.- Extracolonic Tumors.- Surveillance.- MUTYH Associated Polyposis.- Peutz-Jeghers Syndrome.- Clinical Aspects of Juvenile Polyposis.- Hereditary Mixed Polyposis Syndrome and Multiple Adenoma Patients.- Hyperplastic Polyposis.- Genetic Counseling Overview.- Across Culture and Health Systems - Europe.- Across Culture and Health Systems - Asia (Hong Kong).- Across Culture and Health Systems - Asia (Japan).- Across Culture and Health Systems - Africa.- Across Culture and Health Systems - Argentina.- Across Culture and Health Systems - Australia.- Across Culture and Health Systems - Korea.- Across Culture and Health Systems - America.- Psychological Impact of Genetic Counseling and Testing for Hereditary Colorectal Cancers.- Chemoprevention For Inherited Colorectal Cancer.- Registries

Blurb

Early detection of colorectal cancers is a significant and relatively recent achievement. Persons who carry genetic mutations linked to hereditary colorectal cancer make up 20% of the patient population. With the advent of molecular genetics and the description of hereditary colorectal cancer syndromes, clinicians and genetic counselors are able to use genetic predisposition testing as an effective and important way to identify patients and families affected by inherited colorectal cancer syndromes. Hereditary Colorectal Cancer is a comprehensive collection that documents not only Familial Adenomatous Polyposis and the Lynch syndrome, but also less understood syndromes, including the Hamartomatous Polyposis Syndromes and MutYH Associated Polyposis. Internationally recognized clinicians and researchers further delve into the evolution and potential of syndromes, genes and molecular alterations that have yet to be defined. Instrumental experts in this field of discovery were carefully selected by the section editors to create this premier reference work for clinicians, scientists and researchers confronted with the treatment and management of hereditary colorectal cancer.