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  • Autoimmune Liver Disease: Management and Clinical Practice ,1/e

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    도서명: Autoimmune Liver Disease: Management and Clinical Practice ,1/e
    정   가: 260,000원
    판매가: 247,000원
    적립금: 4,940원 (2%)
    저   자: James Neuberger
    출판사: Wiley
    ISBN  : 9781119532606
    출판일: 2020.02
    판   형: Hardcover
    수량: 수량증가수량감소
    판   수: 1/e
    면   수: 336 page
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    Autoimmune Liver Disease: Management and Clinical Practice ,1/e 수량증가 수량감소 (  4940)
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    의학서적전문 "성보의학서적"의 신간의학도서입니다.


    A practical guide to autoimmune liver diseases through pathogenesis, diagnosis, and management
    In Autoimmune Liver Disease Management and Clinical Practice, practitioners will learn about the current state of autoimmune liver disease and how to focus on their diagnosis and treatment. The four-part book begins with a thorough investigation of current immunological thinking as it relates to the autoimmunity of the liver. It also covers the four major hepatic autoimmune liver diseases in both adults and children, their management and the role of liver transplantation, and learned approaches to patient management and empowerment.
    Expert authors in the field have come together to provide a thorough examination of autoimmune liver disease to help support clinicians assisting patients. The text provides an in-depth look at topics including:
    ● The four major hepatic autoimmune liver diseases, their diagnosis, and potential disease management
    ● The use (and misuse) of autoantibodies in diagnosis and treatment
    ● The role and timing of liver transplantation and the impact of recurrent autoimmune liver disease as well as de novo autoimmune hepatitis
    ● Optimal approaches to managing patients and keeping care personalised
    With breadth, depth and current-day relevance, Autoimmune Liver Disease sheds light on recent developments in management of liver disease for practitioners, nurses, and health care professionals.


    -도서목차-


    Preface xv
    Contributors xvii
    Abbreviations xxi
    Introduction: The Paradigm and Paradox of Liver Autoimmunity 1
    M. Eric Gershwin
    Section I Scientific Basis of Clinical Autoimmune Liver Diseases 3
    1 Introduction to the Physiology, Immunology and Pathology of the Liver and Biliary Tree 5
    Marco Carbone and Mario Strazzabosco
    Key Points 5
    Liver Cell Types and Organization 6
    Hepatic Metabolism 7
    Bilirubin Metabolism and Transport 7
    Carbohydrate Metabolism 7
    Lipid Metabolism 8
    Protein Metabolism 8
    Metabolic Zonation 8
    Hepatic Transport Systems 9
    Basolateral (Sinusoidal) Transporters 9
    Apical (Canalicular) Transporters 11
    Drug Metabolism 11
    Bile Formation, Secretion and the Enterohepatic Circulation 12
    Bile Acid Synthesis and Metabolism 13
    Enterohepatic Bile Acid Circulation 13
    Death and Regeneration of Hepatocytes 14
    Cell Death 14
    Liver Regeneration 15
    Cholangiocyte Reaction to Biliary Damage 16
    Protective Role of Biliary HCO3 − Secretion 16
    Cholangiocytes and Immunity 16
    Biochemical Markers and Patterns of Hepatic Injury 17
    Hepatocellular Necrosis 18
    Cholestasis 18
    References 20
    2 Concepts of Autoimmunity Relevant to Autoimmune Liver Diseases 21
    Isaiah G. Roepe and John M. Vierling
    Key Points 21
    Introduction 22
    Role of Innate and Adaptive Immunity in Autoimmunity in the Context of the Liver as an Immune Organ 22
    Overview 22
    Innate Immunity 23
    Liver as an Innate Immune Organ 25
    Adaptive Immunity and Adaptive Immune Functions of the Liver 25
    Role of the Liver as an Adaptive Immune Organ 28
    Generation and Maintenance of Tolerance to Self‐antigens 28
    Overview 28
    Central Tolerance 29
    Central T‐cell Tolerance 29
    Central B‐cell Tolerance 29
    Peripheral Tolerance 30
    T‐ and B‐cell Clonal Anergy 30
    T‐cell Mediated Immune Regulation 30
    Natural and Inducible T Regulatory Cells 30
    Peripheral B‐cell Regulatory Mechanisms 31
    Regulatory Dendritic Cells 31
    Immunoregulatory Interplay Between Treg and Th17 Cells 31
    Risk Factors for Autoimmune Diseases 31
    Genetics 31
    Complex Genetic and Monogenic Diseases 31
    HLA Risk Alleles 32
    Non‐HLA Gene Associations 32
    Critical Role of Epigenetics 33
    Transcription Factor Enhancers and Super Enhancers 33
    MicroRNAs 33
    Sex and Sex Hormones 33
    Vitamin D and Sunlight Exposure 34
    Loss of Immune Tolerance to Autoantigens and Perpetuation of Autoimmune Diseases 34
    Overview 34
    Role of the Microbiome 35
    Mechanisms of Loss of Tolerance to Autoantigens 35
    Bacterial and Viral Infections 35
    Molecular Mimicry of Autoantigens 36
    Neoantigens 36
    Failure of Apoptosis to Conceal Autoantigens and Eliminate Autoreactive Cells 36
    Immune Deviation of Activated T Cells 37
    T‐cell Receptor Revision in the Periphery 37
    Perpetuation of Autoimmune Diseases 37
    Epigenetics 37
    Epitope Spreading 38
    Tissue Memory T Cells 38
    Cytokines Promoting Chronic Inflammation and Autoimmunity 38
    Tertiary Lymphoid Structures and Germinal Centers 39
    Epithelial Cell‐induced Transformation of iTreg to Th17 Cells 39
    Prevention of Autoimmunity and Therapeutic Control of Autoimmune Diseases 39
    Overview 39
    Strategies to Prevent Autoimmunity 39
    Vitamin D3 39
    Gut Microbiota Manipulation in Pregnancy and Infancy 39
    Oral Tolerance 39
    Strategies to Treat Established Autoimmune Diseases 40
    Inducible T Regulatory T Cells 40
    Epigenetic Enhancer Regulation 40
    References 44
    3 Genetics and Risk of Autoimmune Liver Diseases 47
    George F. Mells
    Key Points 47
    Introduction 48
    HLA Associations in Autoimmune Liver Disease 50
    Non‐HLA Associations in Autoimmune Liver Disease 53
    Conclusion 61
    References 62
    4 Autoantibodies and Understanding of Autoimmune Liver Diseases 65
    Benedetta Terziroli Beretta‐Piccoli, Giorgina Mieli‐Vergani, and Diego Vergani
    Key Points 65
    Introduction 66
    Methods of Detection 66
    Anti‐nuclear Antibody 68
    History 68
    Immunofluorescence Reactivities and Antigenic Targets 68
    Clinical Significance in Autoimmune Liver Disease 70
    Ani‐smooth Muscle and Anti‐actin Antibodies 73
    History 73
    Immunofluorescence Reactivities, Antigenic Targets, and Clinical Significance 73
    Anti‐liver‐kidney Microsomal Antibody 74
    History 74
    Immunofluorescence Reactivities, Antigenic Targets, and Clinical Significance 75
    Anti‐liver Cytosol Type 1 Antibody 76
    History 76
    Immunofluorescence Reactivities, Antigenic Targets, and Clinical Significance 76
    Anti‐soluble Liver Antigen Antibody 76
    History 76
    Immunofluorescence Reactivities, Antigenic Targets, and Clinical Significance 77
    Ani‐neutrophil Cytoplasmic Antibody 77
    History 77
    Immunofluorescence Reactivities, Antigenic Targets, and their Clinical Significance 77
    Anti‐mitochondrial Antibody 78
    History 78
    Immunofluorescence Reactivities, Antigenic Targets, and their Clinical Significance 78
    Anti‐asialoglycoprotein Receptor Antibody 79
    History 79
    Immunofluorescence Reactivities, Antigenic Targets, and their Clinical Significance 79
    Indications for Autoimmune Liver Serology Testing 79
    Concluding Remarks 81
    References 82
    5 Environmental Exposure and Risk in Autoimmune Liver Diseases 83
    Ying Qi Li and Andrew L. Mason
    Key Points 83
    Introduction 84
    Autoimmunity 84
    Interaction of Genes and Environmental Triggers in Autoimmunity 85
    Mechanisms for Triggering Autoimmunity 86
    Primary Biliary Cholangitis 89
    Geo‐epidemiology, Clusters, and Case–Control Studies of PBC 92
    Bacterial Infection and PBC 93
    Xenobiotics and PBC 96
    Viruses in PBC 97
    Autoimmune Hepatitis 99
    Prospectus 101
    References 102
    Section II Autoimmune Liver Diseases and Their Clinical Correlation 103
    6 Autoimmune Hepatitis 105
    Aliya Gulamhusein and Patrick McKiernan
    Key Points 105
    Introduction 106
    Definition and Pathophysiology 106
    Epidemiology 107
    Presentation 108
    Adult‐onset AIH 108
    Pediatric‐onset AIH 109
    Diagnosis 109
    Autoimmune Sclerosing Cholangitis 112
    Treatment 112
    Therapeutic Approach in Adults 113
    First-line Therapy 113
    Withdrawal of Therapy 114
    Second‐line Options 114
    Therapeutic Approach in Children 115
    First-line Therapy 115
    Withdrawal of Therapy 115
    Second‐line Options 115
    Prognosis 116
    Adulthood 116
    Childhood 116
    References 118
    7 Primary Biliary Cholangitis 123
    Alessio Gerussi and Marco Carbone
    Key Points 123
    Introduction and Definition 124
    Epidemiology 124
    Etiopathogenesis 125
    Clinical Presentation 126
    Asymptomatic Patients 126
    Symptomatic Patients 126
    Diagnosis 127
    Biochemical Tests 127
    Autoantibodies 128
    Liver Biopsy 128
    Imaging 130
    Differential Diagnosis 130
    Natural History 130
    Disease Course in the UDCA Era 131
    Risk Stratification 132
    Treatment 134
    Ursodeoxycholic Acid 134
    Obeticholic Acid 135
    Fibric Acid Derivatives 136
    Budesonide 137
    Liver Transplantation 137
    Symptom Management 137
    Complications of Liver Disease 139
    Osteoporosis 139
    Advanced Liver Disease 140
    Varices 140
    HCC 140
    Useful Websites 141
    References 141
    8 Primary Sclerosing Cholangitis 143
    Mette Vesterhus, Benedetta Terziroli Beretta‐Piccoli, Kirsten Muri Boberg, and Giorgina Mieli‐Vergani
    Key Points 143
    Introduction 144
    Definition 145
    Adult PSC 145
    Epidemiology 145
    Diagnosis 146
    Diagnosis of Variant Phenotypes 147
    Presentation 147
    Malignancy 149
    Cholangiocarcinoma 149
    Gallbladder Cancer 150
    Colorectal Cancer 150
    Prognosis 150
    Risk Stratification: Clinical Characteristics 150
    Natural History Models 151
    ALP and Bilirubin 151
    Non‐invasive Evaluation of Fibrosis 151
    Treatment 152
    Medical Treatment 152
    Bile Acid Therapy 153
    Microbiota Modulators 153
    Anti-inflammatory Treatment 154
    Antibiotic Therapy 154
    Endoscopic Treatment 154
    Surveillance for Malignancy 154
    Colorectal Cancer: Colonoscopy 155
    Gallbladder Cancer: Ultrasound 155
    Hepatocellular Cancer: Ultrasound 155
    Cholangiocarcinoma 155
    Bone Mineral Density 155
    Juvenile Sclerosing Cholangitis 155
    Epidemiology in Pediatric Disease 155
    Autoimmune Sclerosing Cholangitis 156
    Diagnosis in Children 156
    Clinical Features in Pediatric Disease 158
    Treatment of Pediatric Disease (ASC and Juvenile PSC) 158
    Prognosis in Pediatric Disease 159
    Conclusion 159
    References 160
    9 IgG4‐Related Liver and Biliary Disease 163
    Eleanor Barnes and Emma L. Culver Key Points 163
    Introduction and Historical Perspective 164
    Etiology and Pathogenesis of IgG4‐RD 165
    Development and Characteristics of an IgG4 Antibody Response 165
    Antigens That May Drive an IgG4‐RD Response 166
    IgG4 Antibodies and Pathogenesis 167
    Incidence and Prevalence of IgG4‐RD 167
    Clinical Characteristics of IgG4‐related Hepatobiliary Disease 168
    Hepatobiliary Disease 168
    Disease Outside te Hepatobiliary System 168
    Diagnostic Criteria, Histologic Features, and Approach to Diagnosis of IgG4‐related Hepatobiliary Disease 168
    Diagnostic Criteria for AIP and IgG4‐RD 168
    Histologic Diagnosis of IgG4‐related Hepatobiliary Disease 170
    Utility of Blood Tests, Including Serum IgG4 Levels in IgG4‐RD Diagnostics 171
    Common Alternative Diagnoses to Consider 172
    Radiologic Characteristics of Hepatobiliary IgG4‐RD 173
    IgG4‐RD and Relationship with Malignancy 173
    Management and Treatment of Patients with IgG4‐RD 174
    Monitoring and Follow‐up 175
    Conclusions and Future Directions 175
    References 177
    Section III Specific Clinical Challenges 181
    10 Managing Acute and Chronic Seronegative Liver Disease 183
    Marcus C. Robertson and Peter C. Hayes
    Key Points 183
    Introduction 184
    An Approach to Seronegative Acute Liver Failure 184
    Potential Causes of Seronegative ALF and Features that Suggest an Autoimmune Pathogenesis 185
    Clinical Features of Seronegative ALF 188
    Risk Stratification in Seronegative ALF 188
    Management of Seronegative ALF 189
    N‐Acetylcysteine 190
    Corticosteroids 190
    Emergency Liver Transplantation 191
    An Approach to Cryptogenic Chronic Liver Disease 192
    Potential Causes of Seronegative Chronic Liver Disease and Features that Suggest an Autoimmune Pathogenesis 192
    Non‐alcoholic Fatty Liver Disease 194
    Wilson Disease 194
    Seronegative Autoimmune Hepatitis 195
    Seronegative Primary Biliary Cholangitis 197
    Conclusion 197
    References 198
    11 Managing Pregnant Women with Autoimmune Liver Disease 201
    Eleni Theocharidou and Michael A. Heneghan
    Key Points 201
    Introduction 202
    Fertility in AIH 202
    Pregnancy Outcomes in AIH 202
    Liver‐related Outcomes in Pregnancy 206
    Pregnancy in Cirrhosis 209
    Safety of Medication in Pregnancy 210
    Summary 213
    References 214
    12 Bone Health in Patients with Autoimmune Liver Diseases 219
    Albert Parés and Núria Guañabens
    Key Points 219
    Introduction 220
    Prevalence of Osteoporosis and Fractures 222
    Primary Biliary Cholangitis 222
    Primary Sclerosing Cholangitis 223
    Autoimmune Hepatitis 223
    Pathogenesis 224
    Assessment of Bone Disease 226
    Prevention and Treatment of Bone Loss 227
    General Measures 227
    Pharmacologic Agents 227
    Bisphosphonates 227
    Other Agents 229
    Summary 230
    References 231
    Section IV Transplantation and Its Role in Autoimmune Liver Disease 233
    13 Recurrent Autoimmune Liver Disease and Its Impact on Clinical Practice 235
    Carlos Moctezuma‐Velázquez and Aldo J. Montano‐Loza
    Key Points 235
    Introduction 236
    Primary Biliary Cholangitis 236
    Recurrence of PBC After LT 236
    Diagnosis of PBC After LT 236
    Risk Factors Associated with PBC Recurrence After LT 237
    Treatment of PBC Recurrence After LT 238
    Prognostic Impact of PBC Recurrence After LT 239
    Primary Sclerosing Cholangitis 239
    Recurrence of PSC After LT 240
    Diagnosis of Recurrence of PSC After LT 240
    Risk Factors Associated with PSC Recurrence After LT 240
    Treatment of PSC Recurrence After LT 241
    Prognostic Impact of PSC Recurrence After LT 241
    Autoimmune Hepatitis 241
    Recurrence of AIH After LT 242
    Risk Factors Associated with AIH Recurrence After LT 242
    Treatment of AIH Recurrence After LT 243
    Prognostic Impact of AIH Recurrence After LT 243
    Conclusions 243References 244
    14 Recurrent Autoimmune Liver Disease and its Scientific Significance 247
    Atsushi Tanaka, Patrick S.C. Leung, and M. Eric Gershwin
    Key Points 247
    Introduction 247
    Recurrence of PBC 248
    Incidence and Diagnosis of Recurrent PBC 249
    Risk Factors of Recurrent PBC 250
    Impact of Recurrent PBC on Long‐term Outcomes 250
    Recurrence of PSC 251
    Incidence and Diagnosis of Recurrent PSC 252
    Risk Factors of Recurrent PSC 253
    Impact of Recurrent PSC on Long‐term Outcomes 254
    Recurrence of AIH 254
    Incidence and Diagnosis of Recurrent AIH 254
    Risk Factors of Recurrent AIH 255
    Impact of Recurrent AIH on Long‐term Outcomes 255
    Concluding Remarks 256
    References 257
    Section V Controversies in Autoimmune Liver Diseases 263
    15 Making Sense of Overlap and Crossover Syndromes 265
    Olivier Chazouillères
    Key Points 265
    Introduction 266
    General Considerations 267
    Liver Biopsy 268
    AIH Scores 269
    Genetics 269
    PBC/AIH Overlap Syndrome 269
    PSC/AIH Overlap Syndrome 272
    Liver Transplantation 273
    Conclusions 274
    References 275
    16 The Role of Extrahepatic Autoimmunity in Autoimmune Liver Disease 277
    Ewa Wunsch and Piotr Milkiewicz
    Key Points 277
    Introduction 278
    Epidemiology 278
    Autoimmune Thyroid Disease 279
    Sjogren Syndrome 279
    Systemic Sclerosis 280
    Systemic Lupus Erythematosus 281
    Rheumatoid Arthritis 282
    Celiac Disease 283
    Inflammatory Bowel Disease 284
    Conclusions 286
    Guidelines for Clinicians 287
    References 288
    17 Symptoms, Chronic Disease, and Patient Management 289
    David Jones
    Key Points 289
    Background 290
    Goals of Treatment 290
    Symptoms, Quality of Life, and Health Utility: Key Concepts 291
    Symptoms 291
    Health‐related Quality of Life 292
    Health Utility 292
    Symptoms and Their Management in AILD 292
    Impact of Disease‐modifying Therapy on Symptoms in AILD 292
    Stage‐associated Symptoms 293
    Stage‐independent Symptoms 293
    Pruritus 293
    Fatigue and Cognitive Symptoms 295
    Social Isolation Symptoms 298
    Effective Care Delivery in AILD 299
    References 300
    Index 301


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    - 고객님의 주문으로 수입된 해외 도서인 경우
    - 수령일로 14일 지난 상품의 경우

    - 해외 주문 도서는 고객님의 요청에 의해 주문하는 '개인주문' 상품으로, 단순한 고객변심/착오로 인한 취소, 교환, 반품은 불가능합니다.
    - 해외주문 시 도서가격 및 수입 제반 비용 등을 모두 선결제로 진행하고 재고 관련 등의 사유로 취소, 교환, 반품이 불가능하오니
      이점 꼭 숙지하시고 해외주문시 신중하게 주문하여 주시기 바랍니다.


    반품절차
    - 배송완료후 3일 이내에 고객센터 02-854-2738 혹은 1:1 문의게시판을 통해 교환 및 반품 의사를 알려주세요.
    - 도서는 택배 또는 등기우편으로 보내주시기 바랍니다.
    - 14일 이내에 교환/반품/환불 받으실 상품이 회수되어야 하며, 반품과 환불의 경우 상품주문시 면제받으셨던
      배송비와 반품배송비까지 고객님께서 부담하시게 됩니다.

    반품주소
    (10881) 서울시 구로구 구로중앙로26길 32(구로동) 1층(성보의학서적)
    전화) 02-854-2738

    환불방법
    - 대금은 반품 확인 후에, 카드취소/ 적립금 지급/ 계좌로 환불조치 해 드립니다.
    - 카드결제 시 카드 승인취소절차를 밟게 되며 무통장입금시 현금 환불 혹은 적립금으로 변환 가능합니다.
    - 반품도서와 함께 도서명, 주문번호와 환불계좌번호를 알려주시면 빠른 처리 가능합니다.



    서비스문의

    성보의학서적(Medical Book Store) 전화: 02) 854-2738 팩스: 02) 854-2808 이메일: medcore15@naver.com

    고객센터: (02)854-2738

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