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Liver: A Complete Book on Hepato-Pancreato-Biliary Diseases - E-Book

Liver: A Complete Book on Hepato-Pancreato-Biliary Diseases - E-Book

Mamun-Al Mahtab

(2012)

Additional Information

Book Details

Abstract

The spectrum and etiology of liver diseases vary widely between East and West and hence the focus and experience of hepatologists also remain varied at two corners of the globe. Hepatology being perhaps one of the most flourishing and evolving discipline of medical sciences, a book with recent information written by experts from all over the world was much needed. The present book fulfills this need.

The book will serve as a useful reference manual to consultants, postgraduate students, and residents of Hepatology, Gastroenterology, Internal Medicine, Pathology, Virology, and Preventive Medicine as well as undergraduate clinical medical students.

Liver is a comprehensive book that discusses all aspects of diseases ranging from epidemiology to prognosis. This book is unique in its conception and presentation, as not only it provides new information but also offers a balanced and rational approach to diseases of liver, pancreas, and biliary system. One of the characteristic features of the book is inclusion of diseases of pancreas and separate chapters on important topics like cytokines and chemokines and apoptosis in liver diseases, as a sound background in these is essential for becoming a good specialist. It contains a chapter on evidence-based clinical practice in hepatology, which is the basis of modern clinical practice. It also includes a chapter on preventive aspects of hepato-biliary diseases keeping in mind that prevention of diseases is always preferred to cure.

One of the unique features of this book is, it has contributors from all over the world.


Table of Contents

Section Title Page Action Price
Front Cover\r Front Cover
Front Matter\r i
Copyright\r iv
Foreword\r vii
Preface\r ix
Acknowledgements x
Contributors xi
Contents xvii
Section I basics In Hepatology\r 1
Chapter 1 - Anatomy and Histology of the Liver 3
Anatomy 3
Lobes of the Liver 3
The Peritoneal Connections 4
Bile Ducts 4
Blood Supply 4
Embryology 4
Histology 4
Hepatocytes 5
Nuclei 6
Cytoplasm 6
Bile Ducts 7
Endothelial Cells 7
Sinusoidal Endothelial Cells 7
Other Endothelial Cells 8
Macrophages 8
Stellate Cells 8
Hemopoietic Cells 8
Extracellular Matrix 8
Chapter 2 - Hepatocellular Function 10
Structure of the Liver 10
Evaluation of Hepatocellular Function 11
Metabolic Functions of the Liver 11
Carbohydrate Metabolism 11
Fat Metabolism 11
Protein Metabolism 11
Immunological Function 12
Miscellaneous Metabolic Functions of the Liver 12
Bile Acid Metabolism 12
Bile Secretion 12
Storage of Vitamins 12
Storage of Iron 12
Removal or Excretion of Drugs, Hormones, and Other Substances 12
Excretion of Bilirubin in the Bile 12
Chapter 3 - Apoptosis in Liver Disease 14
Introduction 14
Factors Involved in Regulation of Apoptosis 14
Mechanisms of Regulation of Apoptosis 14
Elimination of Apoptotic Liver Cells 15
Apoptosis and Liver Disease 15
Viral Hepatitis 15
Hepatitis A 15
Hepatitis B 15
Hepatitis C 15
Other Viruses 15
Autoimmune Hepatitis 15
Hepatocellular Carcinoma 15
Cholestatic Liver Diseases 15
Primary Biliary Cirrhosis 16
Primary Sclerosing Cholangitis 16
Obstructive Jaundice 16
Drug-Induced Liver Disease 16
Alcoholic Liver Disease 16
Methods of Studying Apoptosis 17
Conclusion 17
Chapter 4 - Cytokine and Chemokine in Liver Disease 19
Cytokines as Immune Mediators 19
Adaptive Immune Response in Viral Hepatitis 19
Inflammation 21
Fibrosis 21
Alcoholic Liver Disease and Hepatitis C Virus 21
Nonalcoholic Steatohepatitis 22
HIV-HCV Co-Infection 23
Chapter 5 - Preventive Aspects of Hepatobiliary Diseases 25
Spectrum of Liver Diseases and Prevention 25
Prevention of Viral Hepatitis 25
Hepatitis A and E 25
Immunization Against Hepatitis A 26
Active Immunization 26
Passive Immunization 26
Hepatitis B, C, and D 26
Prevention of Hepatitis B and D 26
Precautions for Modifying Risk Factors 26
Injection Safety 26
Patient-Care Equipment 26
Work Environment 26
Hand Hygiene and Gloves 26
Abstinence or Reduced Alcohol Intake 26
Safe Sex Practices 27
Caution Regarding Intimate Contact 27
Active Immunization 27
Postexposure Prophylaxis 27
Prevention of Hepatitis D 27
Prevention of Hepatitis C 27
Prevention of Cirrhosis 27
Prevention of Hepatocellular Carcinoma 27
Prevention of Alcoholic Cirrhosis 28
Liver Abscesses 28
Prevention of Liver Abscesses 28
Prevention of Pyogenic Liver Abscess 28
Prevention of Gall Stones 28
Cholesterol Gall Stones 28
Prevention of Drug-Induced Hepatitis 28
Autoimmune Hepatitis 29
Prevention of Liver Fluke Infection 29
Chapter 6 - Bioethics in Hepatology 30
Introduction 30
Impact of Genetic Testing 30
Types of Genetic Testing 31
Principles of Genetic Testing and Counseling 32
Respect for the Autonomy of Persons 32
Informed Consent 32
Nondirectiveness 33
The Right not to Know 33
Privacy and Confidentiality 34
Genetic Testing for Vulnerable Groups 34
Ethical and Legal Resources Related to Genetic Testing 34
Conclusion 35
Chapter 7 - Evidence-Based Clinical Practice in Hepatology 36
Introduction 36
The Evidence Hierarchy 36
Does The Trial Have A Sufficient Sample Size And Has It Been Properly Estimated? 38
What Are The Risks Of Bias In The Trial? 39
Generation Of The Allocation Sequence 39
Allocation Concealment 39
Blinding 40
Are There Statistical Analyses Of Entry Data? 40
Are The Statistical Analyses Of The Outcomes In Accordance With The Trial Protocol And Are They Intend To Treat? 40
Who Are The Participants And Which Outcomes Are Reported? 40
Which Experimental Intervention Has Been Used? 40
Which Comparator Has Been Used: Placebo Or Active? 41
The Basic Design Of The Trial: Parallel-Group Or Cross-Over Randomized Trial? 41
Multiple Promising Interventions: The Factorial Design 41
Cluster Randomized Trials 41
What Is The Goal Of The Trial? 42
Conflicts Of Interests 42
Systematic Reviews And Meta-Analyses 43
Section II\r Assessing The Liver 45
Chapter 8 - Liver Function Tests 47
Introduction 47
Liver Injury Markers 48
Alanine and Aspartate Aminotransferases 48
Lactate Dehydrogenase 49
Cholestasis Markers 49
Alkaline Phosphatases 49
γ-Glutamyl Transpeptidase and 5' Nucleotidase 49
Markers of Liver Clearance of Metabolites and Drugs 50
Clearance of Bilirubin 50
Clearance of Ammonia 51
Markers of Liver Synthetic Function 51
Prothrombin Time 51
Albumin 52
Serum Protein Electrophoresis 52
Liver Fibrosis Biomarkers 52
Hyaluronic Acid Test 52
Combinations of LFTs as Markers of Liver Fibrosis 53
Panels of Biomarkers 54
Panels of Biomarkers for Fibrosis and Necroinflammatory Activity 54
Panels of Biomarkers for Liver Steatosis 54
Noninvasive Tests: Future Perspectives 54
Specific Biochemical and Serologic Tests for Liver Diseases 55
Conclusion 55
Chapter 9 - Hepatic Imaging 57
Introduction 57
Imaging Techniques 57
Conventional Radiography 57
Ultrasonography 57
Computed Tomography 58
Magnetic Resonance Imaging 58
Nuclear Scintigraphy 59
Imaging of Focal Liver Disease 59
Benign Liver Lesions 59
Hepatic Cysts 59
Hemangiomas 59
Focal Nodular Hyperplasia 60
Hepatic Adenomas 60
Biliary Cystadenomas and Cystadenocarcinomas 60
Focal Infection 60
Malignant Liver Lesions 61
Hepatocellular Carcinoma 61
Cholangiocarcinoma 61
Intrahepatic or Peripheral Cholangiocarcinoma 61
Hilar and Distal Extrahepatic Cholangiocarcinoma 62
Metastases 62
Imaging of Diffuse Liver Disease 62
Cirrhosis 62
Iron Overload (Hemochromatosis and Hemosiderosis) 63
Steatohepatitis and Fatty Liver 63
Budd-chiari Syndrome 63
Conclusion 64
Chapter 10 - Liver Biopsy 65
Introduction 65
Indications 65
Relative Contraindications 66
Preprocedure Evaluation 66
Coagulopathy Assessment 66
Choice of Modality for Image Guidance 66
Needle Selection 66
Technique 66
Complications 67
Chapter 11 - Histopathological Changes in Liver Diseases 69
Introduction 69
Technical Aspects of the Evaluation of Liver Tissue 69
Tissue Biopsy 69
Fixation and Sectioning 70
Special Histochemical Stains 70
Special Techniques 72
Immunohistochemistry 72
Immunofluorescence 72
Electron Microscopy 73
In Situ Hybridization 73
Special Microscopy 73
Other Newer Techniques 73
General Approach to the Morphological Evaluation of Liver Tissue 74
Gross Examination 74
Microscopic Examination 75
Terminology in Hepatic Histopathology 75
Specific Liver Diseases 82
Developmental Anomalies 82
Metabolic Diseases 84
Cholestasis and Biliary Tract Diseases 88
Fatty Liver Disease 90
Infections 91
Viral Hepatitis-acute and Chronic 91
Bacterial Infections 92
Fungal Infections 93
Parasitic Infestations 93
AIDS and Liver 93
Hepatic Fibrosis and Cirrhosis 94
Vascular Disorders 96
Granulomatous Liver Disease 97
Autoimmune Liver Disease 98
Liver in Systemic Disease 99
Masses of Liver-non-Neoplastic and Neoplastic 100
Benign Lesions of Liver 100
Malignant Lesions of Liver 103
Liver Transplant Rejection and Other Complications 104
Chapter 12 - Hematological Changes in Liver Diseases 107
Introduction 107
Morphological Changes in Blood Cells in Liver Disease 108
Macrocytosis 108
Target Cells 108
Stomatocytes 108
Acanthocytes 109
Echinocytes 109
Spherocytes 109
Schistocytes 109
Anemia in Liver Disease 109
Acute Blood Loss 109
Chronic Gastrointestinal Blood Loss with Resultant Iron Deficiency 109
Folic Acid and Vitamin B12 Deficiency 110
Hemolysis 110
Zieve's Syndrome 110
Spur Cell Hemolytic Anemia 110
Hemolysis Associated with Wilson's Disease 110
Hemolysis Associated with Hepatitis C Infection 110
Splenic Pooling and Sequestration 111
Inadequate Erythropoietin Response 111
Myelosuppression 111
Leucopenia and Leucocytosis 111
Thrombocytopenia and Impaired Platelet Function 111
Aplastic Anemia 112
Coagulation 112
Overview of Coagulation and Fibrinolysis 112
Coagulation and Liver Disease 113
Impaired Synthesis of Coagulation Factors 113
Impaired Clearance of Activated Coagulation Factors 114
Vitamin-k Deficiency 114
Enhanced Fibrinolysis and Dysfibrinogenemia 114
Disseminated Intravascular Coagulation 115
Warfarin and Liver Disease 115
Liver Transplantation 115
Cholestatic Liver Disease 115
Kasabach-merritt Syndrome 115
Pregnancy-Related Conditions 115
Hematological Complications of Hepatitis C Infection 116
Cryoglobulinemia 116
Lymphoma and Other Lymphoproliferative Disorders 116
Autoimmune Cytopenias 117
Hepatitis B Infection and Non-Hodgkin Lymphoma 117
Hematological Effects of Alcohol 117
Peripheral Blood 117
Bone Marrow Cytology 117
Bone Marrow Histology 118
Polycythemia and Liver Disease 118
Hepatic Manifestations of Hematological Disorders 118
Lymphoma and the Liver 119
Hematological Causes of the Budd-chiari Syndrome 120
Hepatic Complications of Hematopoietic Stem Cell Transplantation 120
Veno-Occlusive Disease 120
Graft-Versus-Host Disease 120
Conclusions 120
Section III\r Congenital Liver Diseases 123
Chapter 13 - Congenital Hyperbilirubinemias 125
Introduction 125
Unconjugated Hyperbilirubinemia 125
Gilbert's Syndrome 125
Epidemiology 125
Etiology 125
Mode of Inheritance 126
Clinical Features 126
Diagnosis 126
Treatment and Prognosis 127
Crigler-Najjar Syndrome 128
Epidemiology 128
Etiology 128
Mode of Inheritance 128
Clinical Features 128
Diagnosis 129
Treatment and Prognosis 129
Conjugated Hyperbilirubinemia 130
Rotor's Syndrome 130
Etiology 130
Clinical Features 130
Diagnosis and Treatment 130
Dubin-Johnson Syndrome 130
Etiology 131
Clinical Features 131
Diagnosis 131
Treatment and Prognosis 131
Chapter 14 - Wilsons Disease 132
Introduction 132
Pathophysiology 132
Clinical Features 132
Hepatic Presentation 133
Neurological Presentation 133
Psychiatric Presentation 133
Renal Tubular Acidosis 133
Orthopedic Involvement 133
Ocular Involvement 133
Other Presentations 133
Diagnosis 133
Serum Ceruloplasmin 133
Serum Copper 134
Urinary Copper 134
Hepatic Copper Estimation 134
Liver Histology 134
Making the Diagnosis of Wilson's Disease Causing Fulminant Liver Failure 134
Genetic Studies 134
Treatment 135
Penicillamine 135
Trientine 135
Zinc 136
Treatment During Pregnancy 136
Diet 136
Liver Transplantation 136
Other Agents 136
Copper Overload Disorders Other than Wilson's Disease 136
Chapter 15 - Hereditary Hemochromatosis 138
Introduction 138
History 138
Genetics 138
HFE-Related Hemochromatosis 138
Non-HFE-Related Hemochromatosis 139
Pathophysiology 140
Clinical Features 140
Clinical Classification Of Hemochromatosis 141
Diagnosis 141
Genotyping 141
Liver Biopsy 141
Treatment 142
Family And Population Screening 143
Chapter 16 - Alpha-1 Antitrypsin Deficiency 144
Introduction 144
History 145
The AAT protein 145
Nomenclature 146
The AAT Gene and its Evolution 146
Function 147
Biosynthesis of AAT 147
Prevalence of AAT Deficiency 148
Genetic Epidemiology of AAT Deficiency 148
Far East and Asia 148
Developing Countries 148
Natural History 148
Clinical Recognition of AAT Deficiency 149
Genetic Testing for AAT Deficiency 149
Diagnostic Testing 149
Pre-Dispositional Testing 150
Assessment of Carrier Status in Relation to Reproduction 150
Population Screening 150
Identification of Individuals with AAT Deficiency 150
Early Detection Prenatal 150
Detection in Adults 150
Symptoms 151
Physical Findings 151
Laboratory Tests 152
Quantitative Tests 152
Qualitative Tests 152
Risk Factors 152
Pathophysiology of AAT Deficiency 153
Liver Disease 154
Mechanism of Liver Damage 155
Diagnosis and Management 155
Follow-Up 156
Therapy 156
Prevention 157
Chapter 17 - Glycogen Storage Disease 158
Introduction 158
Epidemiology 158
Etiology and Genetic Background 158
Pathology 158
Type I Glycogenosis (Gierke Disease) 160
Pathomechanism 160
Clinical Picture 160
Treatment 160
Type II Glycogenosis (Pompe Disease) 160
Type III Glycogenosis (Cori Disease) 161
Chapter 18 - Porphyria 164
Introduction 164
Classification 164
Pathomechanism 164
Acute hepatic porphyrias 165
Clinical picture 165
Differential diagnosis 166
Therapy 166
Nonacute porphyrias 166
Porphyria cutanea tarda 166
Pathomechanism and genetic background 167
Clinical picture 167
Differential diagnosis 167
Therapy 167
Protoporphyria erythropoietic 168
Epidemiology, genetic background and pathomechanism 168
Clinical picture 168
Congenital erythropoietic porphyria 168
Hepatoerythropoietic porphyria 169
Symptomatic (secondary) porphyrias 169
Epilog 169
Section IV Jaundice\r 171
Chapter 19 - Hepatocellular Jaundice 173
Definition of Jaundice 173
Pathphysiology (Bilirubin Metabolism) 173
Clinical Presentations of Jaundice Patients 174
Hepatomegaly with or without Pain 174
Coagulation Disturbances 175
Circulatory Changes 175
Causes of Hepatocellular Jaundice 175
Acute Hepatocellular Jaundice 175
Acute Viral Hepatitis 175
Symptoms and Sign 175
Diagnosis 176
Treatment 176
Acute Hepatitis Due to Other Viruses 176
Infectious Mononucleosis 176
Cytomegalovirus 176
Yellow Fever 176
Herpes Simplex 176
Other Infectious Agent 176
Toxoplasmosis 176
Liver Damage Caused by Drugs 176
Hepatocellular Necrosis 176
Chronic Liver Disease 177
Miscellaneous Acute Reactions 178
Diagnosis and Treatment 178
Hepatic Ischemia 178
Ischemic Hepatitis 178
Hepatic Infarction 179
Ischemic Cholangiopathy 179
Acute Liver Failure (Acute Fulminant Hepatitis) 179
Etiology 179
Hemodynamic Monitoring 180
General Management 180
Liver Transplantation 180
Chronic Hepatocellular Jaundice 181
Chronic Hepatitis 181
Etiology and Classification 181
Alcoholic Liver Disease 181
Fatty Liver (Steatosis) 181
Hepatitis 181
Cirrhosis 181
Chapter 20 - Prehepatic Jaundice 187
Normal Metabolism of Hemoglobin to Bilirubin 187
Hemolysis, Ineffective Hemopoiesis, and Jaundice 187
Harmful Effects of Prehepatic Jaundice 188
Congenital Constitutional Causes of Hemolytic Jaundice 188
Hereditary Spherocytosis 188
Other Membrane Defects 189
Pyruvate Kinase Deficiency 189
G6PD Deficiency 189
Hemoglobinopathies 190
Other Inherited Hemolytic Anemia 190
Congenital Constitutional Causes of Ineffective Hemopoiesis-Thalassemia 190
Chapter 21 - Cholestatic Liver Disease 192
Introduction 192
Normal Bile Formation And Secretion 192
Molecular Mechanisms And Pathophysiology Of Cholestasis 193
Clinical Features Of Cholestasis 194
Biochemical Alterations In Cholestasis 194
Intrahepatic Cholestasis Versus Extrahepatic Cholestasis 194
Imaging In Cholestasis 195
Liver Histopathology 195
Differential Diagnosis Of Intrahepatic Cholestasis 196
Treatment 196
Drug-Induced Cholestasis 197
Pure Cholestasis 198
Cholestatic Hepatitis 198
Cholestatic Hepatitis Associated With Bile Duct Injury 198
Vanishing Bile Duct Syndrome 198
Large Bile Duct Strictures 198
Section V \rhepatotropic Viruses 199
Chapter 22 - Hepatitis A Virus 201
Introduction 201
Definition 201
Virology 201
Structure Of The Virus (Fig. 22-1) 201
Steps Of Viral Replication 201
History 202
Epidemiology 202
Clinical Types Of Hepatitis A 202
Acute Hepatitis 202
Cholestatic Hepatitis 202
Relapsing Hepatitis 203
Fulminant Hepatic Failure 203
Hepatitis A In Pregnancy 203
Laboratory Tests 203
Histopathology 203
Prevention 204
Prophylaxis 204
Preexposure Prophylaxis 204
Hepatitis A Vaccine 204
Indications 204
Postexposure Prophylaxis 204
Treatment 204
Chapter 23 - Hepatitis E Virus 206
Introduction 206
Hepatitis E Virus 206
The Virus And Genome Organization 206
Viral Proteins 206
Replication Cycle 207
Genetic Variation 207
Epidemiology 208
Transmission 209
Clinical Features 209
Serological And Other Tests 209
Serosurveys 210
Animal Models 210
Vaccine Development 210
Conclusion 212
Chapter 24 - Hepatitis B Virus 213
Introduction 213
Virology Of HBV 213
Molecular Virology 213
Life Cycle 213
Epidemiology Of Hepatitis B 214
Geographic Distribution 214
HBV Genotypes 214
Modes Of Transmission 215
Natural History Of HBV Infection 216
Clinical Dynamics Of HBV Infection 216
Diagnosis 217
Clinical Manifestations 217
Acute HBV Infection 218
Chronic HBV Infection 218
HBeAg Positive Chronic Hepatitis B 218
HBeAg Negative Chronic Hepatitis B 218
Inactive HBsAg \"carrier\" state 219
Cirrhosis Of Liver And HCC 219
Extra Hepatic Manifestations 219
Management Of Hepatitis B Infection 219
Evaluation Of Patients 219
Goals Of Treatment 220
Prevention Of HBV Infection 220
Chapter 25 - Hepatitis B Virus: Mutants 221
Introduction 221
HBV Mutants 221
Surface Gene Mutations 222
Core Gene Mutations 223
Precore Gene Mutations 223
X-gene Mutations 223
Polymerase Gene Mutations 223
Chapter 26 - Hepatitis B Virus: Advances In Management 225
Introduction 225
Advances In The Prophylaxis Of HBV 225
Advances In The Management Of HBV 226
Management Of Patients With Chronic HBV Infection 226
Management On The Basis Of Better Understanding About HBV Genome And Viral Life Cycle 226
Management On The Basis Of Advances In Natural History Of HBV 227
Advancement In Understanding About Pathogenesis Of Chronic HBV Infection And Their Utility In Patient Management 228
Conclusion 228
Chapter 27 - Hepatitis C Virus 229
The Hepatitis C Virus Discovery And Nomenclature 229
Epidemiology Of Hepatitis C Infection 229
Natural History Of HCV 230
HCV Coinfection With HIV And HBV 230
HCV And Alcohol 230
Extrahepatic Manifestations Of HCV Infection 231
Global Distribution Of HCV Genotype 231
Treatment Of Chronic Hepatitis C 231
Type I IFNs 231
Ribavirin 232
Therapy For Chronic HCV With Pegylated-IFN And Ribavirin 232
Management Of Patients 232
Patients With Genotype 1 HCV 232
Patients With Genotypes 2 And 3 HCV 233
Other Genotypes 233
Difficult Patient Groups 233
Management Of Side Effects Of Therapy 233
Future Developments 234
Conclusion 234
Chapter 28 - Hepatitis D Virus 235
History 235
Virion Structure 235
HDV Genome 235
Hepatitis D Antigen 235
Lipoprotein Envelope of HDV 236
HDV Life Cycle 236
HDV Infection 236
Coinfection 236
Superinfection 236
Pathogenesis of HDV-Induced Hepatitis 237
Natural History of Hepatitis D 237
Epidemiology of HDV Infection 237
The Mediterranean Basin 237
The Far East 237
Western Countries 238
HDV in South East Asia 238
HDV Genotypes 238
Genotype I 238
Genotype II 238
Genotype III 238
Impact of HDV on HBV 238
Diagnosis of HDV Infection 239
Detection of Serum HDV AG 239
Detection of Serum HDV RNA 239
Detection of Anti-HDV Antibody 239
Tissue Markers of HDV Infection 239
Clinical Presentations of HDV Infection 240
Acute Hepatitis B Virus Infection 240
Acute Hepatitis of Undetermined Origin in a Chronic HBV Carrier 240
HBSAG-Positive Chronic Liver Disease 240
Treatment 240
Clinical Course of HDV Infection 240
AIMS of Treatment 240
Treatment of Acute HDV Infection 240
Treatment of Chronic HDV Infection 241
Interferon Alfa 241
Trials of Therapy 241
Pegylated IFN 242
Other Treatment Options 242
Current Recommendations for Treatment 243
Future Perspectives for Treatment 243
Prevention of HDV Infection 244
Summary 244
Chapter 29 - Other Hepatitis Viruses 245
Introduction 245
GBV-C or HGV 245
TTV and Related Viruses 245
Section VI Autoimmune Liver Diseases\r 247
Chapter 30 - Autoimmune Hepatitis 249
Introduction 249
Epidemiology 249
Etiopathogenesis of AIH 250
Clinical Features 250
Demography 250
Symptoms 250
Signs 250
Associated Diseases with AIH 250
Natural History 251
Laboratory Features 251
Diagnosis 251
Basic Diagnostic Tests 251
Clinical Criteria 252
Scoring System 252
Established Autoantibodies 252
Antinuclear Antibody 252
Antismooth Muscle Antibody 253
Anti-Lkm1 Antibody 253
Perinuclear Antineutrophil Cytoplasmic Antibodies 253
Histopathology 254
Types 254
Type 1 AIH 254
Type 2 AIH 254
Type 3 AIH 255
Variants 255
Overlap Syndrome with PBC 255
Overlap Syndrome with PSC 255
Autoimmune Cholangitis 255
Cryptogenic (Autoantibody Negative) Chronic Hepatitis 256
Concurrent AIH with Chronic Viral Hepatitis 256
Treatment 256
Indications for Treatment 256
Treatment Regimens 256
Side Effects of the Drugs 256
Monitoring of Patients on Treatment and During Follow Up 257
Treatment End-Points and Further Course of Action 257
Treatment Results 258
Remission 258
Treatment Failure 258
Incomplete Response 258
Survival 259
Promising Drugs 259
Liver Transplantation 259
Chapter 31 - Primary Biliary Cirrhosis 261
Introduction 261
Epidemiology 261
Genetic Factors 262
Etiology and Pathogenesis 262
Molecular Mimicry 262
Environmental Factors/Xenobiotics 262
Microbial Infection 263
Immune Response 263
Antimitochondrial Autoantibodies 263
Adaptive Immunity/T-cell Responses Against Mitochondrial Antigens 264
Innate Immunity in PBC 264
Antinuclear Antibodies in PBC 264
Biliary Epithelial Cells 265
Apoptosis and Liver Injury in PBC 265
Clinical Features 265
Presentation 265
Asymptomatic PBC 265
Symptomatic PBC 266
Symptoms and Disease Complications 266
Fatigue 266
Pruritus 266
Jaundice 266
Xanthomata and Xanthelasma 266
Abdominal Pain 267
Portal Hypertension 267
Metabolic Bone Disease 267
Steatorrhea and Fat Soluble Vitamin Malabsorption 267
Hepatocellular Carcinoma 267
Associated Disorders 267
Autoimmune Disorders 267
Gastrointestinal Diseases 268
Pulmonary Disorders 268
Renal Tubular Acidosis 268
Laboratory Tests 268
Biochemical Features 268
Serological Features 268
Liver Histology 269
Diagnosis 269
Differential Diagnosis 269
Autoimmune Cholangitis 270
PBC and Aih Overlap Syndrome 270
Natural History and Prognosis 270
Asymptomatic PBC 270
Symptomatic PBC 271
Prognostic Survival Models 271
Medical Treatment 271
Symptomatic Treatment 271
Pruritus 271
Sicca Syndrome 272
Raynaud's Syndrome 272
Hypercholesterolemia 272
Preventive Treatment 272
Osteoporosis 272
Portal Hypertension 272
Treatment of Underlying Liver Disease 272
Ursodeoxycholic Acid 272
Immunosuppressive Therapy 273
Antifibrotic Agents 273
Combination Therapy 273
Liver Transplantation 273
Chapter 32 - Primary Sclerosing Cholangitis 275
Introduction 275
Epidemiology 275
Prevalence of PSC in IBD 276
Etiology and Pathogenesis 276
Immunogenic Factors 276
Infections 277
Diagnosis 277
Laboratory Investigations 277
Radiological Features 277
Histology 277
Special Populations 278
Small Duct PSC 278
Overlap Diseases 278
Management of Complications 278
Dysplasia and Cancer 278
Other Complications 278
Nonspecific 278
Specific 279
Transplant 279
Prognosis 279
Section VII \rInfluence Of Drugs Andenvironment On Liver 281
Chapter 33 - Drug-Induced Liver Diseases 283
Introduction 283
Diagnosis 283
Epidemiology 283
Management 284
Conclusion 284
Chapter 34 - Arsenic-Induced Liver Disease 285
Introduction 285
The Arsenicosis Map and Its Impact 285
Metabolism of Arsenic 285
Health Effects of Arsenic Exposure 286
Arsenic and Liver Diseases 286
Epidemiological Study 286
Arsenic and Hepatic Fibrosis 287
Mechanisms of Injury 288
Arsenic and Liver Cancer 289
Chapter 35 - Alcoholic Liver Disease 291
Introduction 291
Epidemiology 291
Disease Spectrum 292
Alcoholic Fatty Liver 292
Alcoholic Hepatitis 292
Cirrhosis 292
Pathophysiology 292
Oxidative Injury 292
Cytokine and Immune-Mediated Injury 293
Contributory Factors 293
Sex 293
Malnutrition 293
Viral Hepatitis 293
Clinical Presentation 293
Pathology 294
Diagnosis 295
Screening 295
Laboratory Values 295
Role of Liver Biopsy 295
Treatment of Ald 295
Abstinence 296
Glucocorticoids 296
Cytokine-Directed Therapies 296
Nutritional Therapies 297
Other Therapies 297
Prognosis Criteria 298
Liver Transplantation for ALD 298
Chapter 36 - Nonalcoholic Fatty Liver Disease 300
Introduction 300
Prevalence 300
General Population 300
At Risk Groups 300
Obesity 300
Diabetes Mellitus 300
Metabolic Syndrome 301
Other Insulin-Resistant States 301
Natural History 301
Diagnosis 301
Clinical and Laboratory Features 301
Imaging 302
Biopsy 302
Pathogenesis 302
Insulin Resistance-Peripheral or Hepatic? 302
Additional Factors 303
Oxidative Stress 303
Mitochondrial Dysfunction 303
Adipocytokines 303
Other Potential Damaging Factors 304
Impaired Fat Handling Within the Hepatocyte 304
Genetic Factors 304
Dietary Factors 304
Treatment of NAFLD 305
Nonpharmacological Approach for Insulin Resistance 305
Weight Reduction 300
Diet 305
Exercise 305
Antiobesity Agents 306
Orlistat 306
Sibutramine 306
Cannabinoid Receptor Antagonist 306
Bariatric Surgery 306
Insulin-Sensitizing Agents 307
Metformin 307
Thiazolidinediones 307
Fibrates 308
Hepatoprotective Agents 308
Antioxidant/Anticytokine Agents 308
Ursodeoxycholic Acid 309
Pentoxifylline 309
Vitamin E (-tocopherol) 309
Betaine and SAMe 309
The Use of HMG Co a Reductase Inhibitor (Statins) in NAFLD 309
Other Potential Therapies 309
Angiotensin II Blockade 309
Section VIII\rLiver Failure 311
Chapter 37 - Acute Liver Failure 313
Introduction 313
Definition 313
Classification 313
Incidence 314
Etiologies of ALF 314
Nonacetaminophen-Induced ALF 314
Acetaminophen-Induced ALF 315
Other Drugs Implicated in ALF 315
Causes of ALF 316
Vascular 316
Metabolic 316
Miscellaneous 316
Prognosis 316
Different Diagnostic Criteria 316
King's College Criteria 317
Clichy Criteria 317
Meld and ALF 317
Pathogenesis of Hepatic Encephalopathy Due to ALF 318
Investigations for the Etiology of ALF 318
Management of ALF 318
Initial Management 319
Paracetamol-Induced ALF 319
Nonparacetamol-Induced ALF 319
Specific Management 319
Encephalopathy 319
Clinical Manifestations 319
Monitoring of ICP 320
Treatment 320
Experimental Therapies 321
Induction of Hypothermia 321
Prophylactic Phenytoin 321
Induction of Hypernatremia 321
Complications 321
Cardiovascular and Pulmonary Complications 321
Renal Complications 321
Treatment 322
Metabolic Disturbances 322
Infection and Sepsis 322
Malnutrition 323
Coagulopathy 323
Liver Transplantation and Support Systems 323
Unhelpful Treatments 323
Newer Approaches 323
Artificial Hepatic Assist Devices 324
Auxiliary Liver Transplantation 324
Liver Support Systems 324
Xenotransplantation 324
Chapter 38 - Liver Dialysis 325
Introduction 325
Principles of MARS and Role of Albumin 325
Impact on Central and Local Hemodynamics 326
Impact on Kidney Function 327
Impact on Central Nervous Function 328
Impact on Liver Function and Cytokine Profile 328
Impact on Pruritus 329
Conclusion 329
Section IX \rCirrhosis And Complications 331
Chapter 39 - Cirrhosis of Liver 333
Introduction 333
From fibrosis to cirrhosis 333
Epidemiology 334
Classification of Cirrhosis 335
Morphological Classification of Cirrhosis 335
Etiology of Cirrhosis 335
Clinical Presentation 336
Symptoms 336
Physical Examination Findings 336
Hepatocellular Dysfunction 337
Jaundice 337
Skin Findings 337
Hand Findings 337
Palmar Eythema 337
Dupuytren's Contracture 337
Nail Changes 337
Clubbing and HOA 338
Asterixis (Flapping Tremor) 338
Gynecomastia 338
Testicular Atrophy 338
Findings Related to Portal Hypertension 338
Splenomegaly 338
Ascites 338
Dilated Abdominal Veins 339
Cruveilhier-Baumgarten Murmur 339
Fetor Hepaticus 339
Other Features 339
Eye Signs 339
Hepatomegaly 339
Clinical Conditions Associated with Liver Cirrhosis 339
Type II Diabetes 339
Bacterial Infections 340
Malnutrition 340
Extrahepatic Autoimmune Diseases 340
Chronic Relapsing Pancreatitis and Pancreatic Calcifications 340
Peptic Ulcer Disease 340
Diagnosis of Cirrhosis 340
Laboratory Findings 340
Hematology 340
Serum Biochemistry 341
Serological, Immunological, or Genetic Tests in Liver Cirrhosis 341
Imaging in Liver Cirrhosis 342
Liver Biopsy 342
Complications of Cirrhosis 343
Prognosis of Cirrhosis 344
Treatment of cirrhosis 345
Liver Transplantation for End-Stage Liver Cirrhosis 346
Chapter 40 - Hepatic Encephalopathy 348
Introduction 348
Burden of HE 348
Nomenclature and Grading of HE 349
Diagnosis of HE 350
Pathogenesis of HE 350
Ammonia 350
GABA/Endogenous Benzodiazepines 350
Infection/Inflammation 351
Treatment of HE 351
Management of Precipitating Factors 351
Dietary Proteins 351
Nonabsorbable Disaccharides 351
Antibiotics 352
Probiotics 352
l-ornithine l-aspartate (LOLA) 352
Oral Zinc 352
Sodium Benzoate 352
Flumazenil 352
Branched Chain Amino Acids 352
Bromocriptine 352
Minimal Hepatic Encephalopathy 353
Historical Aspects 353
Clinical significance of MHE 353
Diagnostic Tools for MHE 353
Neuropsychological assessment 353
EEG 354
Critical flicker frequency 354
Diagnosis of MHE 354
Treatment of MHE 354
Nonabsorbable Disaccharides 355
Prebiotics and synbiotics 355
Is It Time to Recognize and Treat MHE? 356
Chapter 41 - Portal Hypertension: Pathophysiology 357
Introduction 357
Embryology 357
The Portal Vein 357
Hepatic Arterial Supply 357
Control of Intrahepatic Circulation 358
Definition of Portal Hypertension 358
Basic Hemodynamics 358
Pathogenesis 358
Increased Resistance 358
Factors that Control Stellate Cell Contractility 359
Vasoconstrictors 360
Adrenergic Agonists 360
Angiotensin II 360
Endothelins 360
Vasodilators 360
Nitric Oxide 360
Carbon Monoxide 360
Prostaglandins 360
Cannabinoids 360
Increased Portal Venous Flow 361
Increased Hepatic Arterial Flow 361
Clinical Features of Portal Hypertension 361
Etiology of Portal Hypertension 361
Presinusoidal Portal Hypertension 362
Portal Vein Thrombosis 362
Schistosomiasis 362
Idiopathic Portal Hypertension 362
Sinusoidal Portal Hypertension 362
Alcoholic Liver Disease 362
Hepatitis B 362
Hepatitis C 362
Postsinusoidal Portal Hypertension 363
Budd-Chiari Syndrome 363
Conclusions 363
Chapter 42 - Portal Hypertension: Management 364
Introduction 364
Etiology 364
Pathophysiology Of Portal Hypertension 365
Diagnosis 365
Endoscopy 365
Pulsed Doppler Together With Abdominal Ultrasonography 365
Portal Pressure Measurements 365
Endosonography 365
Measurement Of Variceal Pressure 365
Natural History And Clinical Manifestations Of Portal hypertension 365
Esophageal Varices 365
Gastric Varices 365
Ectopic Varices 366
Portal Hypertensive Gastropathy 366
Management Of Variceal Bleed 366
Preprimary Prophylaxis 366
Primary Prophylaxis 366
Pharmacological Treatment 366
Nonselective -Blockers 366
Organic Nitrates 366
Spironolactone 366
Endoscopic Therapy 366
Endoscopic Sclerotherapy 366
Endoscopic Variceal Ligation 366
Acute Variceal Hemorrhage 366
Resuscitation 366
Antibiotic Prophylaxis 367
Pharmacological Treatment 367
Vasopressin 367
Terlipressin 367
Somatostatin 367
Octreotide 367
Endoscopic Treatment 367
Emergency EST 367
Emergency EVL 367
Balloon Tamponade 367
Chapter 43 - Ascites 370
Introduction 370
Definition 370
Prevalence 370
Pathogenesis 370
Clinical Aspects 371
Diagnosis and Investigation 371
Complementary Studies 371
Classification 372
Uncomplicated Ascites 372
Refractory Ascites 372
Management of Ascites 372
General Measures 372
Specific Measures 372
Bed Rest 372
Sodium Restriction 372
Therapeutic Paracentesis 373
Diuretics 374
Peritoneovenous Shunt 374
Transjugular Intrahepatic Portosystemic Shunt 375
Liver Transplantation 376
Prognosis 376
Section \tX \rLiver In Cardiovascular Diseases 379
Chapter 44 - Budd-Chiari Syndrome 381
Introduction 381
Pathology 382
Clinical Features 382
Prognosis 383
Diagnosis 383
Real Time Doppler Sonography 383
Hepatic Venography 383
Liver Biopsy 384
Treatment 384
Liver Decompression 384
Surgical Shunt 384
Do Shunts Improve Liver Histology and Fibrosis? 384
TIPS 385
Liver Transplantation 385
Chapter 45 - Extrahepatic Portal Vein Obstruction 386
Introduction 386
Etiology 386
In Children 386
In Adults 386
Clinical Features 386
Pathology 388
Diagnosis 389
Laboratory Abnormalities 389
Prognosis 389
Treatment 389
Chapter 46 - Hepatic Vena Cava Disease 390
Introduction 390
Nomenclature of the Disease 390
History of HVD 391
Epidemiology of HVD 392
Etiology of HVD 392
Congenital Vascular Malformation Theory (Hirooka 1969) 392
Thrombosis Theory (Okuda 1986) 392
Thrombophlebitis Theory 392
Pathophysiology of HVD 393
Acute Disease 393
Chapter 47 - Liver in Congestive Cardiac Failure 399
Introduction 399
Congestive Hepatopathy 399
Clinical Features and Diagnosis 400
Clinical Course 400
Treatment 400
Cardiogenic Ischemic Hepatitis 400
Diagnosis 401
Clinical Course 401
Treatment 401
Congestive Liver Fibrosis and Congestive Cirrhosis (Cardiac Cirrhosis) 401
Diagnosis 402
Treatment 402
Cardiac Drugs in Hepatic Dysfunction 402
Chapter 48 - The Liver in Shock 403
Introduction 403
Acute Right Heart Failure 403
Acute Left Heart Failure 403
Chronic Passive Congestion (Cardiac Sclerosis) 404
Shock Liver 404
Treatment and Prognosis 405
Section XI \rNon-Viral Infections Of Liver 407
Chapter 49 - Amebic Liver Abscess 409
Introduction 409
Epidemiology 409
Etiology 410
The Organism 410
Life Cycle 410
Morphology of ALA 410
Pathogenesis 411
Clinical Features 411
Demography 411
Symptoms 411
Atypical Presentations 412
Complications 412
Diagnosis 413
Laboratory Findings 413
Imaging 413
Stool Examination 413
Serology 414
Diagnostic Aspiration 414
Differential Diagnosis 414
Treatment 414
Prognosis 415
Prevention 416
Chapter 50 - Pyogenic Liver Abscess 417
Introduction 417
Epidemiology 417
Etiology 417
Biliary Tree 417
Hematogenous Dissemination of Microorganism 417
Direct Extension from a Contiguous Focus of Infection 418
Trauma 418
Cryptogenic 418
Predisposing Factors 418
Microbiology 418
Organism by Source of Infection 418
Clinical Manifestations 418
Laboratory Findings 419
Imaging Studies 419
Microbial Cultures 419
Difference Between Amebic and PLA 419
Treatment 420
Antibiotic Therapy 420
Abscess Drainage 420
Percutaneous Drainage of PLA 420
Percutaneous vs. Surgical Drainage 420
Endoscopic Retrograde Cholangiopancreatography 420
Prognosis 420
Chapter 51 - Hydatid Disease of Liver 422
Introduction 422
Epidemiology 422
Characteristics of the Parasite and Cycle 422
Hepatic Hydatid Disease in Humans 424
Diagnosis 425
Clinical Presentation 425
Clinical Laboratory 426
Imaging 427
Therapy 435
Surgical Therapy 436
Indications of Surgical Therapy 436
Preoperative Work-Up 436
Hepatic Hydatidosis Surgery 436
Treatment of the Parasite 436
Managing the Pericystic Membrane or Adventitia 436
Comparison between Conservative and Radical Techniques 438
Hydatid Relapse after Surgical Therapy 438
Laparoscopic Surgery 439
Chemotherapy 439
Percutaneous Procedures 440
Complications of Hepatic Hydatidosis 441
Biliary Complications 441
Suppurated Hydatid Cyst 442
Peritoneal Rupture 442
Thoracic Complications of Hepatic Hydatidosis 443
Chapter 52 - Human leptospirosis 445
Introduction 445
Historical Aspects 446
Etiological Agent 446
Classification 446
Modes of Transmission 447
Environmental Factors 447
Occupational Factors 447
Epidemiology 447
Clinical Picture and Manifestations 449
Septicemic Phase 450
Immune Phase 450
Pathogenesis and Pathology 451
Hemorrhagic Form 451
Hepatic Form 451
Renal Form 451
Myocardial Form 452
Pulmonary Form 452
Ophthalmic Lesions 452
Meningeal Lesions 452
Diagnostic Approaches 452
Laboratory Diagnosis 452
Blood and Urinary Profile 452
Microscopic Methods 453
Dark-Field/Phase Contrast Microscopy 453
Silver Impregnation 453
Fluorescent Method 453
Serological Methods 453
Macroscopic Agglutination Test 453
Microscopic Agglutination Test 453
Microcapsule Agglutination Test 453
Enzyme-linked Immunosorbent Assay 454
Lepto-dipstick 454
Latex Agglutination Test 454
Indirect Hemagglutination Test 454
Complement Fixation Test 454
Molecular Methods 454
Nucleic Acid Hybridization 454
Polymerase Chain Reaction 454
Ribotyping Methods 454
Pulsed-field Gel Electrophoresis 454
Restriction Enzyme Analysis 454
Culture 454
Animal Inoculation 455
Differential Diagnosis 455
Treatment 455
Prognosis 455
Prevention and Control 456
Conclusion 456
Section XII \rLiver Diseases In Pregnancy And Childhood 457
Chapter 53 - Pregnancy and Liver Diseases 459
Introduction 459
Liver in Normal Pregnancy 459
Intrahepatic Cholestasis of Pregnancy 459
Toxemias 460
Hellp Syndrome 460
Acute Fatty Liver of Pregnancy 460
Hepatic Rupture and Hemorrhage 461
Acute Viral Hepatitis in Pregnancy 461
Other Liver Diseases in Pregnancy 461
Chapter 54 - Pediatric Liver Diseases 463
Introduction 463
Infants 464
The Jaundiced Infant 464
Unconjugated hyperbilirubinemia 464
Differential diagnosis of unconjugated hyperbilirubinemia in neonates 464
Crigler-Najjar syndrome types 1 and 2 464
Gilbert's syndrome 464
Conjugated hyperbilirubinemia 464
Differential diagnosis of conjugated hyperbilirubinemia 464
Biliary atresia 465
Choledochal cysts 467
Caroli disease in infancy 467
Neonatal sclerosing cholangitis 467
Endocrine causes of neonatal conjugated hyperbilirubinemia 467
Chromosomal causes of conjugated hyperbilirubinemia 468
Progressive familial intrahepatic cholestasis 468
Alagille's syndrome, arteriohepatic dysplasia, syndromic paucity of bile ducts, Watson-Miller syndrome 469
Peroxisomal disorders 470
Infections 470
Acute liver failure in infancy 471
HIV 471
Leishmaniasis 471
Tuberculosis 471
Dengue infection 472
Tyrosinemia type 1 472
Galactosemia 472
Inborn errors of metabolism 472
Mitochondrial disorders 473
Neonatal hemochromatosis (NNH) 473
Familial hemophagocytic lymphohistiocytosis 474
Neonatal lupus erythematosus 474
Hepatosplenomegaly in infancy 474
Glycogen storage disorders 475
Lysosomal storage disorders 475
Gaucher disease 475
Niemann Pick disease 475
Older children 476
Infections in Older Children 476
Hepatitis A 476
Hepatitis E 476
Herpesviruses 476
Treatment of herpesvirus infection 476
Parvovirus B19 476
Group A streptococcus 476
Tuberculosis 477
Malaria 477
Prevention 477
Typhoid fever 477
Dengue fever 477
Leptospirosis 477
Seronegative hepatitis (Non A-G hepatitis) 477
Treatment 477
Liver Abscess 477
Presenting features 477
Diagnosis 477
Predisposing factors 478
Treatment 478
Drug-Induced Liver Disease 478
Presenting features 478
Section XIII \rSpace Occupying Lesions Of Liver 491
Chapter 55 - Benign Liver Lesions 493
Introduction 493
Hepatocellular Lesions 493
Hepatocellular Adenoma 493
Epidemiology 493
Pathogenesis 494
Macroscopic Appearance 494
Microscopic Appearance 494
Presentation 494
Natural History 494
Diagnosis 494
Laboratory Investigations 494
Imaging 495
Management 495
Focal Nodular Hyperplasia 495
Epidemiology 495
Pathogenesis 496
Macroscopic Appearance 496
Microscopic Appearance 496
Presentation 496
Natural History 496
Diagnosis 496
Management 497
Nodular Regenerative Hyperplasia 497
Epidemiology 497
Pathogenesis 497
Macroscopic Appearance 497
Chapter 56 - Hepatocellular Carcinoma 505
Introduction 505
Epidemiology, Risk Factors, And Pathogenesis 505
Clinical Features 506
Screening, Surveillance, And Diagnosis 506
Serological Markers 507
Alpha-Fetoprotein 507
Other Serological Markers 507
Radiological Imaging Of HCC 508
Ultrasonography 508
CT Scanning 508
MR Imaging 508
Histological Confirmation 509
Screening Protocols 509
Staging And Prognosis 509
Management Of HCC 509
Surgical Resection 510
Liver Transplantation 510
Ablative Approaches 513
Percutaneous Ethanol Injection 513
Cryosurgery 513
Radiofrequency Ablation 514
Transarterial Chemoembolization 514
Other Ablative Modalities 514
New Frontiers 515
Prevention Of HCC 515
Conclusions 515
Chapter 57 - Hepatic Metastases 517
Introduction and Epidemiology 517
Imaging Techniques 517
Computed Tomography 517
Magnetic Resonance Imaging 518
Ultrasonography 518
Hepatic Angiography and CT Portography 518
Inferior Vena Cavography 519
Positron Emission Tomography 519
Laparoscopic Staging 519
Classification 519
Hepatic Metastases from Colorectal Cancer 520
Incidence 520
Natural History 520
Treatment 520
Liver Resection 520
Rationale 520
Decision Making 521
Prognosis 523
Basingstoke Predictive Index 523
Molecular Determinants of Outcome 523
Repeat Resection for Recurrent Disease 524
Laparoscopic Resection 524
Long-term Results 524
Medical Treatment 525
Systemic Chemotherapy 525
HAI Chemotherapy 525
Neoadjuvant Chemotherapy 526
Nonresective Destructive Techniques 527
Radiofrequency Ablation 527
Cryoablation 527
Brachytherapy 527
High Intensity Focused Ultrasound (HIFU) 527
Others 527
Conclusion 527
Neuroendocrine Hepatic Metastases 528
Classification of NECs 528
Small Intestine Carcinoids 528
Pancreatic Neuroendocrine Cancers 528
Treatment 529
Liver Resection 529
Liver Transplantation 529
Radiofrequency, Ethanol, and Cryoablation 529
Medical Treatment 529
Primary Hepatic Neuroendocrine Tumors 529
Section XIV \rSurgery And Liver 533
Chapter 58 - Liver Transplantation 535
Introduction 535
Indications for Liver Transplantation 535
Patient Evaluation 537
Pretransplantation Management Issues 537
Waiting-List Monitoring of Hepatitis B Liver Transplant Candidates 537
Waiting-List Monitoring and Treatment of Hepatitis C Liver Transplant Candidates 537
Adjunctive Treatment and Staging of Hcc Transplant Candidates 538
Living Donor Liver Transplantation: Indications, Donor Evaluation, and Outcome 538
LDLT for Hepatocellular Carcinoma 539
Perioperative Complications 539
Long-Term Complications after Liver Transplantation 540
Opportunistic Infections 540
Chronic Rejection 540
Calcineurin Inhibitor-Induced Nephrotoxicity 541
Other Side Effects of CNI 541
De Novo Malignancies 542
Biliary Complications 542
Metabolic Bone Disease 543
Recurrent Diseases after Liver Transplantation 543
Recurrence of Hepatitis C in the Allograft 543
Recurrence of Hepatitis B in the Allograft 544
Recurrence of Cholestatic Liver Diseases and AIH 545
Tumor Recurrence 546
Recurrent Alcohol Abuse after Liver Transplantation for Alcoholic Liver Disease 547
Outcome of Liver Transplantation in Hiv Patients 547
Experiences with Liver Transplantation in Inherited Metabolic Liver Diseases 547
Outcome after Liver Transplantation for Acute Hepatic Failure 548
Conclusion 548
Chapter 59 - Surgery in Liver Diseases 550
Recent Advances in Liver Resection for Hepatocellular Carcinoma 550
Indication for Safe Hepatectomy 550
Ultrasound-Guided Hepatectomy 550
Inflow Occlusion for Hepatectomy 551
PVE before Hepatectomy 551
Summary 551
Section XV \rDiseases Of Gallbladder And Biliary Tree 553
Chapter 60 - Gallstone Disease 555
Introduction 555
Composition of Gallstones 555
Prevalence 556
Risk factors (Table 60-1) 556
Genetic and Racial Factors 556
Sex 556
Pregnancy and Parity 556
Obesity 556
Weight Loss 557
Total Parenteral Nutrition 557
Dietary Factors 557
Hyperlipidemia 557
Drugs 557
Cirrhosis 557
Hemolysis 557
Pathogenesis 557
Cholesterol Gallstones 557
Nucleating and Antinucleating Factors 558
Gallbladder Hypomotility 558
Recent Advances in Pathogenesis of Gallstones 558
Pathogenesis of Pigment Stones 558
Black Pigment Stones 558
Natural History of Gallstone Disease 559
Clinical Manifestations of Gallstone Disease 559
Gallstones and Gallbladder Cancer 559
Gallstones and Xanthogranulomatous Cholecystitis 559
Diagnosis 560
Management of Gallstones (Table 60-5) 560
Asymptomatic Gallstones 561
Symptomatic Gallstones 561
Comparison of Open Cholecystectomy and Laparoscopic Cholecystectomy 561
Nonoperative Therapies 562
Acute Cholecystitis 562
Choledocholithiasis 562
Chapter 61 - Other Gallbladder Diseases 564
Introduction 564
Anatomy 564
Acute Acalculous Cholecystitis 565
Acute Hydrops Gallbladder 565
Adenomyomatosis of the Gallbladder 565
Definition 566
Incidence and Prevalence 566
Polyps of Gallbladder 566
Pathology 566
Cholesterol Polyps 566
Inflammatory Polyps 566
Adenomas 566
Clinical Manifestations 566
Treatment 566
Chapter 62 - Carcinoma of Gallbladder 568
Introduction 568
Epidemiology 568
Etiology and Pathogenesis 568
Gallbladder Anatomy: Relevance to Gallbladder Cancer 569
Clinical Presentation 569
Imaging 570
Ultrasonography 570
Computed Tomography Scan 571
Magnetic Resonance Imaging 571
Positive Emission Tomography 571
Staging 571
Laboratory Abnormalities 571
Prognosis 571
Treatment 572
Gallbladder Polyps 572
T1 Tumors 573
T2 Tumors 573
T3 and T4 Tumors 573
Chapter 63 - Cysts and Congenital Biliary Anomalies 574
Introduction 574
Development of the Fetal Liver 574
Congenital Anomalies of the Biliary Tree 574
Choledochal Cysts 574
Caroli's Disease and Caroli's Syndrome 575
Congenital (Simple) Liver Cysts 576
Other Inherited Abnormalities of Extrahepatic Bile Ducts 576
Mesenchymal Hamartoma of the Liver 576
Biliary Atresia 576
Chapter 64 - Benign Biliary Stricture 578
Introduction 578
Anatomy of the Bile Ducts 578
Etiology of Benign Biliary Strictures 578
Bismuth Classification of Benign Postoperative Biliary Strictures 580
Pathogenesis and Pathophysiology 580
Portal Hypertension 581
Effects of Biliary Obstruction 581
Nutritional Effects of Biliary Obstruction 581
Cardiovascular and Renal Effects of Obstructive Jaundice 581
Infectious Complications of Obstructive Jaundice 581
Clinical Presentation 582
Diagnostic Evaluation 582
Liver Function Test 582
Imaging Modalities 583
Ultrasonography 583
Computerized Tomography Scan 583
Cholangiography 583
Magnetic Resonance Cholangiopancreatography 583
Percutaneous Transhepatic Cholangiography 583
Endoscopic Retrograde Cholangiography 583
Hepatobiliary Scintigraphy 583
Endoscopic Ultrasound 584
Intraductal Ultrasound 584
Liver Biopsy 584
Other Investigations 584
Assessing and Accessing Biliary Strictures 585
Management of Biliary Strictures 585
General Measures 585
Biliary Drainage 585
Percutaneous Approach 585
Endoscopic Treatment 586
Surgical Management 587
Biliary Stents in Benign Biliary Strictures 588
Metal Stents 588
Bioabsorbable Stents 588
Nonpostoperative Biliary Strictures 588
Chronic Pancreatitis Related Biliary Strictures 588
Biliary Strictures Following Liver Transplantation 589
Primary Sclerosing Cholangitis 589
Portal Biliopathy 589
Biliary Tuberculosis 589
Aids-Related Biliary Stricture 589
Biliary Parasitosis 589
Conclusions 589
Chapter 65 - Hepatobiliary Ascariasis 591
Introduction 591
Pathogenesis 591
Clinical Manifestations (Tables 65-1 and 65-2) 592
Common Presentations 592
Uncommon Presentations 593
Investigations 593
Treatment 594
Antihelminthic Drugs 594
Endoscopic Interventions 594
Surgery 595
Recurrent Infection 595
Chapter 66 - Cholangiocarcinoma 596
Introduction 596
Classification of cca 596
Epidemiology 597
Etiology and risk factors 598
Pathogenesis 599
Pathology and staging 599
Clinical features 600
Diagnosis 601
Investigations 602
Imaging of the biliary system 602
Management 604
Conclusion 606
Section XVI Diseases Of Pancreas\r 609
Chapter 67 - Acute Pancreatitis 611
Introduction 611
Structure and Function 611
Endocrine Function 612
Exocrine Functions 612
Functional Units 612
Pathophysiology 612
Injury to Acinar Cells 612
Marked Disturbance of Subcellular Membrane Trafficking 612
Activated Neutrophils 612
Macrophages Release Cytokines 612
Epidemiology 612
Incidence 612
Age, Sex, and Race Distribution 613
Relapse Rate 613
Morbidity and Mortality 613
Etiology 613
Gallstones and Biliary Tract Disease (30-60%) 613
Alcohol (30-35%) 613
Idiopathic 614
Post-ercp (8%) 614
Trauma (∼1.5%) 614
Drugs (∼1.4%) 614
Definitely Associated 614
Probably Associated 614
Infection (<1%) 614
Viral 614
Bacterial 614
Ascariasis 614
Aids 614
Hereditary Pancreatitis (< 1%) 615
Hypercalcemia (< 1%) 615
Hyperparathyroidism 615
Developmental and Structural Abnormalities of Pancreas and Biliary System (< 1%) 615
Hyperlipidemia (< 1%) 615
Pregnancy 615
Tumor (< 1%) 615
Postoperative (< 1%) 615
After Organ Transplantation 615
Scorpion and Snake Bite (< 1%) 615
Toxins (< 1%) 615
Clinical Features 616
Complications 616
Intra-abdominal Infections 616
Pancreatic Necrosis 616
Diagnosis 617
Laboratory Tests 617
Pancreatic Enzymes 617
Amylase 617
Lipase 617
Hepatic Enzymes 617
Full Blood Count 617
CRP 617
Blood Culture 617
Fasting Lipid Profile 617
Calcium 617
Urea, Creatinine and Electrolytes, and Blood Sugar 617
Arterial Blood Gases 617
Imaging Studies 617
Plain X-ray of Abdomen 617
Abdominal Ultrasonography 617
CT Abdomen 617
Dynamic Spiral CT 618
Magnetic Resonance Cholangiopancreatography (MRCP) 618
Endoscopic Ultrasonography (EUS) 618
ERCP 618
CT-guided Needle Aspiration 618
Histologic Findings 618
Mild Cases 618
Severe Cases 618
Staging 618
Acute Physiology and Chronic Health Evaluation (APACHE) 618
Management 619
Medical Care 619
Surgical Care 619
Management of Complications 619
Pseudocyst 619
Percutaneous Aspiration 619
Endoscopic Approach 619
Pancreatic Duct Disruption 620
Infected Pancreatic Necrosis 620
Nutritional Management of Pancreatitis 621
Pancreatic Response to Nutritional Intake 621
Nutritional Support in Pancreatitis 621
Jejunal Feeding 622
TPN 622
Total Enteral Nutrition (TEN) 622
Initiation of Enteral Feeding 622
Enteral Feeding in Severe Acute Pancreatitis 622
Criteria for Advancement to Oral Diet 622
Acute Complicated Pancreatitis (or Where Surgery is Needed) 622
Chapter 68 - Chronic Pancreatitis 623
Definition 623
Epidemiology 623
Etiology 623
Alcohol 623
Pancreatic Duct Obstruction 624
Pancreas Divisum 624
Metabolic Changes 624
Sphincter Of Oddi Dysfunction 624
Cystic Fibrosis 624
Hereditary Causes 624
Autoimmune Causes 625
Nutritional Causes 625
Pathophysiology 625
Clinical Features 625
Complications 625
Pain 625
Malabsorption 625
Diabetes Mellitus 625
Pseudocyst Formation 625
Venous Thrombosis 626
Bile Duct Obstruction 626
Duodenal Obstruction 626
Pseudoaneurysm 626
Pancreatic Cancer 626
Diagnosis 627
Histology 627
Pancreatic Exocrine Function Testing 627
Imaging 628
Plain Radiography/Transabdominal Ultrasound 628
Computerized Tomography 629
Endoscopic Retrograde Cholangiopancreatography 629
Endoscopic Ultrasonography 629
Magnetic Resonance Imaging 629
Management 629
Pain Control 629
Analgesics 629
Pancreatic Enzyme Supplements 630
Antioxidants 630
Endoscopic Therapies 630
Denervation Procedures 630
Surgical Options 630
Malabsorption/Exocrine Insufficiency 631
Possible Causes For Poor Response To Pancreatic Enzyme Supplements 631
Diabetes Mellitus 631
Pseudocysts 631
Venous Obstruction 632
Bile Duct Obstruction 632
Duodenal Obstruction 632
Pseudoaneurysm 632
Chapter 69 - Pancreatic Carcinoma 634
Introduction 634
Clinical Features 634
Physical Findings 634
Laboratory Values 634
Differential Diagnosis 635
Diagnostic Procedures 635
Prognosis 635
Operative Findings 636
Resection 637
Chemotherapy 637
Index\r 638
A 638
B 638
C 639
D 639
E 640
F 640
G 640
H 641
I 641
J 642
K 642
L 642
M 642
N 642
O 643
P 643
Q 644
R 644
S 644
T 645
U 645
V 645
W 645
X 645
Y 645
Z 645