Pediatric Hepatology and Liver Transplantation

ISBN-13: 9783319963990 / Angielski / Twarda / 2019 / 829 str.

Lorenzo D'Antiga

Opis

This book is the first to provide balanced examination of both pediatric liver disease and liver transplantation - two topics that are inherently related, given that most chronic liver disorders eventually require organ replacement.

Spis treści

Chapter 1: Liver disease in paediatric medicine: An overview.- Chapter 2: Anatomy and histology of the liver and biliary tract.- Chapter 3: Laboratory evaluation of hepatobiliary disease.- Chapter 4: Diagnostic and interventional radiology.- Chapter 5: Practical approach to the jaundiced infant.- Chapter 6: Biliary atresia and other disorders of the extrahepatic biliary tree.- Chapter 7: Acute liver failure.- Chapter 8: Viral hepatitis.- Chapter 9: Autoimmune liver disease.- Chapter 10: Fibrocystic liver disease.- Chapter 11: Gallstone disease.- Chapter 12: Genetic and familial cholestasis.- Chapter 13: Wilson disease.- Chapter 14: Liver disease in cystic fibrosis.- Chapter 15: Inherited metabolic disorders.- Chapter 16: Non-alcoholic fatty liver disease and steatohepatitis in children.- Chapter 17: Complications of cirrhosis.- Chapter 18: Cirrhotic and non-cirrhotic portal hypertension.- Chapter 19: Vascular liver disease.- Chapter 20: Liver tumours and nodular lesions.- Chapter 21: The liver in systemic illness.-Chapter 22: Nutrition and liver disease.-Chapter 23: Intensive care management of the child with liver disease.- Chapter 24: Peculiarities of common and uncommon indications to liver transplantation.- Chapter 25: Organs availability and allocation.- Chapter 26: Surgical Techniques.- Chapter 27: Living donor liver transplantation.- Chapter 28: Listing for transplantation, postoperative management and f/up protocol.- Chapter 29: Surgical complications.- Chapter 30: Immunosuppression in paediatric liver transplantation.- Chapter 31: Pathology of liver allograft dysfunction.- Chapter 32: Chronic rejection and late allograft hepatitis.- Chapter 33: CMV and EBV infection and disease.- Chapter 34: Liver transplantation for inborn errors of metabolism.- Chapter 35: Immune tolerance following liver transplantation.- Chapter 36: Long-term outcome and transition to adult care.- Chapter 37: Neurodevelopment and Health Related Quality of Life of the Transplanted Child.- Chapter 38: Pediatric Liver Disease In Latin America.- Chapter 39: Liver disease in the African continent.- Chapter 40: Liver disease in the Asian continent.- Chapter 41: Next generation sequencing for the diagnosis of monogenic liver disease.- Chapter 42: Cell therapy for acute and chronic liver disease.- Chapter 43: Gene therapy in paediatric liver disease.

O autorze

Lorenzo D’Antiga is a paediatric Hepatologist and Gastroenterologist working in Italy. His current position is Director of Child Health and of the Paediatric Liver, GI and Transplantation Unit of the Hospital Papa Giovanni XXIII of Bergamo. He trained as a paediatrician at the University of Padua and as a Paediatric Hepatologist in the United Kingdom, at King’s College Hospital London. He has worked as Consultant Gastroenterologist and Hepatologist as well as Paediatric Intensivist, specializing in organ failure and transplantation. ESPGHAN member for 15 years, he contributed to the field of paediatric hepatology with publications, scientific presentation and invited lectures. He has been member of the Council of the ESPGHAN as Education Secretary (till 2014) and member of the Education Committee of the UEG (till 2014). He serves as Senior Associate Editor for Journal of Pediatric Gastroenterology and Nutrition, and as Associate Editor of  Liver Transplantation.

Blurb

This book is the first to provide balanced examination of both pediatric liver disease and liver transplantation – two topics that are inherently related, given that most chronic liver disorders eventually require organ replacement. The different forms of liver disease encountered in the pediatric age group are first discussed in a series of disease-specific chapters that have a reader-friendly, uniform structure covering pathophysiology, diagnostic and treatment algorithms, clinical cases, and transition to adult care. Key topics in the field of liver transplantation are then addressed. Examples include indications and contraindications, surgical techniques and complications, immunosuppression, in pediatric liver transplantation, acute and chronic rejection and allograft dysfunction, and CMV and EBV infection in transplant recipients, long-term graft injury and tolerance. A section on pediatric hepatology across the world includes chapters presenting the features and management of pediatric liver disease in South-America, Africa and Asia. A closing section considers what the future holds for pediatric liver disease and its management, including novel genetic testing, cell therapy and gene therapy. Pediatric Hepatology and Liver Transplantation will be of value for a range of practitioners, from residents making their first approach to pediatric liver disease through to specialists working in transplantation centers.