Hereditary cancer syndromes are linked to alterations in single genes, and detection and clinical interpretation of these alterations can guide cancer risk reduction for patients and their families through screening, prophylactic measures, and other strategies. Diagnosis and Management of Hereditary Cancer summarizes hereditary syndromes and their associated cancers and genes, presented in 50 practice-enhancing tables that relate clinical, genetic, diagnostic, and management aspects.

Format: Hardback
Length: 384 pages
Publication date: 05 July 2021
Publisher: Elsevier Science & Technology

Numerous hereditary cancer syndromes are intricately associated with alterations in single genes, exerting a profound influence on the risk of cancer development. By accurately detecting and comprehending these genetic variations, healthcare professionals can effectively implement screening, preventive measures, and other strategies to mitigate cancer risk for patients and their families. In order to provide a comprehensive understanding of hereditary cancer syndromes and their corresponding cancers and genes, Diagnosis and Management of Hereditary Cancer offers a comprehensive summary. This invaluable resource is presented in a format that facilitates practical application, encompassing 50 practice-enhancing tables that seamlessly integrate clinical, genetic, diagnostic, and management aspects. Designed to cater to both specialists and novice practitioners, this volume aims to elevate the care provided to individuals with hereditary cancer and their families.

Hereditary Cancer Syndromes and Genetic Alterations

Hereditary cancer syndromes are characterized by the presence of genetic mutations that increase the risk of developing certain types of cancer. These syndromes are often caused by alterations in single genes, which can have a significant impact on the development and progression of cancer.

The detection and clinical interpretation of these genetic alterations are crucial in guiding cancer risk reduction for patients and their families. By identifying individuals who are at high risk of developing cancer, healthcare professionals can implement screening programs, such as mammography, colonoscopy, or genetic testing, to early detect the disease. This early detection allows for timely treatment and improved outcomes, reducing the burden of cancer and improving the quality of life for patients.

In addition to screening, genetic counseling can also be provided to patients and their families to help them understand the implications of their genetic mutations and make informed decisions about their care. Genetic counselors can provide information about the risk of developing other cancers, the benefits and risks of genetic testing, and available treatment options. They can also assist patients in navigating the healthcare system and accessing resources and support services.

Diagnosis and Management of Hereditary Cancer is a comprehensive resource that summarizes hereditary syndromes and their associated cancers and genes. This volume is intended to guide both specialists and novice practitioners in the field of hereditary cancer. The information is presented in a manner that is easy to understand and apply, with 50 practice-enhancing tables that relate clinical, genetic, diagnostic, and management aspects in a manner that has previously not been available in a single reference.

The book begins by providing an overview of hereditary cancer syndromes, including their prevalence, characteristics, and associated cancers. It then delves into the genetic basis of these syndromes, discussing the specific genes involved and the mechanisms by which they increase cancer risk. The book also covers the diagnostic process for hereditary cancer, including genetic testing, pedigree analysis, and molecular profiling.

In addition to diagnostic considerations, the book provides comprehensive information about the management of hereditary cancer. It discusses the role of surveillance, screening, and preventive measures, as well as the treatment options available for patients with hereditary cancer. The book also addresses the psychosocial aspects of hereditary cancer, including the impact on patients and their families and the importance of support and counseling.

One of the key strengths of Diagnosis and Management of Hereditary Cancer is its practical approach. The book is filled with examples and case studies that illustrate the application of the information presented in the text. This allows readers to gain a deeper understanding of the complexities of hereditary cancer and how to effectively manage it.

Another notable feature of the book is its emphasis on the multidisciplinary approach to hereditary cancer care. It recognizes that hereditary cancer is a complex disease that requires a team of healthcare professionals, including oncologists, genetic counselors, and other specialists, to provide comprehensive care. The book encourages collaboration and communication between these professionals to ensure that patients receive the best possible care.

In conclusion, Diagnosis and Management of Hereditary Cancer is a valuable resource for healthcare professionals who are involved in the care of individuals with hereditary cancer. By providing a comprehensive summary of hereditary syndromes and their associated cancers and genes, the book helps practitioners to better understand the genetic basis of cancer and implement effective screening, preventive, and treatment strategies. The practical approach and multidisciplinary approach to care make this book an essential tool for improving the care and outcomes of patients with hereditary cancer.

Weight: 726g
Dimension: 161 x 235 x 32 (mm)
ISBN-13: 9780323907460