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Underwood's Pathology

Underwood's Pathology

Simon Cross

(2013)

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Book Details

Abstract

Underwood’s Pathology (formerly General and Systematic Pathology) is an internationally popular and highly acclaimed textbook, written and designed principally for students of medicine and the related health sciences. Pathology is presented in the context of modern cellular and molecular biology and contemporary clinical practice. After a clear introduction to basic principles, it provides comprehensive coverage of disease mechanisms and the pathology of specific disorders ordered by body system. An unrivalled collection of clinical photographs, histopathology images and graphics complement the clear, concise text.

For this sixth edition, the entire book has been revised and updated. Well liked features to assist problem-based learning – including body diagrams annotated with signs, symptoms and diseases and a separate index of common clinical problems – have been retained and refereshed.

Additional value is provided by the complementary online version – hosted on studentconsult.com - which includes the complete, fully searchable text, downloadable images, clinical case studies and a revised, interactive self-assessment section to check your understanding and aid exam preparation. This all combines to make Underwood’s an unsurpassed learning package in this fascinating and most central medical specialty.

  • Contents perfectly matches needs of medical students.
  • Very clinical approach is ideally suited to integrated courses.
  • Each organ system chapter begins with a brief review of normal structure and function, emphasizing aspects that are important to an understanding of the subsequently discussed disease processes.
  • Offers an unrivalled superb collection of clinical photographs, histopathology images, and graphics, approximately 700 in all, that richly depict the appearance of both healthy and diseased tissues.
  • Extensive International Advisory Board validates contents.
  • New co-editor, Dr Simon Cross.
  • Structure of chapters revised to make the book much easier to use during courses that are problem- or case-based.
  • Several new contributors and re-written chapters.
  • Expanded International Advisory Board.

Table of Contents

Section Title Page Action Price
Front cover cover
Underwood's Pathology: a Clinical Approach i
Copyright page iv
Table of Contents v
Preface vi
Acknowledgements vii
International Advisers viii
Contributors ix
Index of Patient Symptoms x
1 Basic Pathology 1
1 What is pathology? 3
History of pathology 4
Morbid anatomy 4
Microscopic and cellular pathology 4
Molecular pathology 5
Cellular and molecular alterations in disease 5
Scope of pathology 5
Clinical pathology 5
Subdivisions of clinical pathology 5
Techniques of pathology 5
Gross pathology 5
Light microscopy 6
Histochemistry 7
Immunohistochemistry and immunofluorescence 7
Electron microscopy 7
Biochemical techniques 7
Haematological techniques 7
Cell cultures 7
Medical microbiology 7
Molecular pathology 7
Learning pathology 7
Disease mechanisms 7
Systematic pathology 7
Building knowledge and understanding 8
Pathology in the problem-oriented integrated medical curriculum 8
The problem-oriented approach 8
The disease-oriented approach 9
Making diagnoses 9
Diagnostic pathology 9
Autopsies 9
Pathology and populations 9
Causes and agents of disease 9
The health of a nation 9
Preventing disability and premature death 10
Further reading 10
2 What is disease? 11
What is disease? 12
Limits of normality 12
Responses to the environment 12
Adaptation 12
Disease: failure of adaptation 12
Darwinian medicine 12
Ageing and adaptation 12
Disease predisposition as an adaptive advantage 13
Characteristics of disease 13
Aetiology 13
Identification of the causes of disease 13
Probability of disease 13
Host predisposition to disease 14
Causes and agents of disease 15
Causal associations 15
Koch’s postulates 16
Pathogenesis 16
Latent intervals and incubation periods 16
Structural and functional manifestations 16
Structural abnormalities 16
Functional abnormalities 17
What makes patients feel ill? 17
Lesions 17
Pathognomonic abnormalities 17
Complications and sequelae 17
Prognosis 17
Remission and relapse 18
Morbidity and mortality 19
Disability and disease 19
Nomenclature of disease 19
Primary and secondary 19
Acute and chronic 19
Benign and malignant 19
Prefixes 20
Suffixes 20
Eponymous names 20
Syndromes 20
Numerical disease coding systems 20
Principles of disease classification 20
General classification of disease 20
Congenital diseases 21
Fetal origins of adult disease 22
Acquired diseases 22
Inflammatory diseases 22
Vascular disorders 22
Growth disorders 22
Injury and repair 22
Metabolic and degenerative disorders 22
Iatrogenic diseases 22
Epidemiology 22
Epidemiological clues to the causes of disease 23
Disease incidence, prevalence, remission and mortality rates 23
Geographic variations 23
Historical changes in disease incidence and mortality 24
Socio-economic factors 25
Occupational factors 25
Hospital and community contrasts 26
Age and disease 26
Common causes of mortality and morbidity 26
Further reading 26
3 What causes disease? 27
Causes of disease 28
Predisposing factors and precursors of disease 28
Prenatal factors 28
Aetiology and age of disease onset 28
Multifactorial aetiology of disease 29
Evidence for genetic and environmental factors 29
Family studies 29
Studies on twins 29
Studies on migrants 29
Association with gene polymorphisms 30
HLA types 30
Blood groups 31
Cytokine genes 31
Gender and disease 31
Racial differences 31
Genetic abnormalities in disease 32
Gene structure and function 32
Nuclear DNA 32
Nuclear genes 33
Gene linkage and recombination 33
Gene transcription and translation 33
Homeobox genes 33
Mitochondrial genes 34
Mitochondria and ageing 34
Techniques for studying genetic disorders 34
Modes of inheritance in families 34
Homozygous and heterozygous states 34
Chromosomal analysis 35
Molecular analysis of genetic disorders 36
Functional and positional genetics 36
Genetic linkages 36
DNA polymorphisms 36
Polymerase chain reaction 37
Diseases due to genetic defects 38
Abnormal chromosome numbers 38
Autosomes 38
Sex chromosomes 38
Fragile sites and chromosomal translocations 38
Single gene defects 38
X-linked single gene disorders 40
Environmental factors 40
Chemical agents causing disease 40
Mechanisms of chemical injury 40
Corrosive effects 40
Metabolic effects 40
Membrane effects 41
Mutagenic effects 41
Allergic reactions 41
Important chemical agents 41
Smoking 41
Alcohol 41
Dusts 41
Drugs 41
Physical agents causing disease 42
Mechanical injury 42
Thermal injury 42
Radiation injury 42
Infective agents 42
Bacteria 43
Bacterial pili and adhesins 44
Bacterial toxins 44
Exotoxins 44
Endotoxins 44
Aggressins 46
Undesirable consequences of immune responses 46
Viruses 47
DNA and RNA viruses 48
Tissue specificity 49
Pathogenesis of cell injury 49
Yeasts and fungi 49
Mycotoxins 52
Parasites 53
Prions 53
Further reading 53
2 Disease Mechanisms 55
4 Disorders of growth, differentiation and morphogenesis 57
Definitions 58
Growth 58
Differentiation 58
Morphogenesis 58
Normal growth, differentiation and morphogenesis 59
Regeneration and replication 59
The cell cycle 59
Molecular events in the cell cycle 60
Duration of the cell cycle 60
Therapeutic interruption of the cell cycle 60
Apoptosis: physiological cell death in growth and morphogenesis 61
Regulation of apoptosis 61
The intrinsic pathway 61
The extrinsic pathway 62
The execution phase 62
Apoptosis in development 62
Differentiation and morphogenesis 63
Control of normal differentiation 63
Cell position and inductive phenomena 63
Control of gene expression in the establishment of phenotype 64
Epigenetic regulation of gene expression 65
Stem cells and transdifferentiation 65
Maintenance and modulation of an attained differentiated state 66
Normal differentiation and morphogenesis: summary 66
Abnormalities of growth, differentiation and morphogenesis 66
Increased growth: hypertrophy and hyperplasia 66
Physiological hypertrophy and hyperplasia 67
Pathological hypertrophy and hyperplasia 67
Apparently autonomous hyperplasias 67
Hyperplasia in tissue repair 68
Skin 70
Liver 70
Heart 71
Decreased growth: atrophy 71
Physiological atrophy and involution 71
Pathological atrophy 71
Decreased function 71
Loss of innervation 71
Loss of blood supply 72
‘Pressure’ atrophy 72
Lack of nutrition 72
Loss of endocrine stimulation 72
Hormone-induced atrophy 72
Decreased growth: hypoplasia 72
Metaplasia 72
Congenital disorders of differentiation and morphogenesis 73
Chromosomal abnormalities affecting whole chromosomes 73
Autosomal chromosomes 73
Sex chromosomes 74
Parts of chromosomes 74
Single gene alterations 74
Enzyme defects 74
Defects in receptors or cellular transport 74
Non-enzyme protein defects 74
Anomalies of fetal development 75
Embryo division abnormalities 75
Teratogen exposure 75
Failure of cell and organ migration 75
Anomalies of organogenesis 76
Agenesis (aplasia) 76
Atresia 76
Hypoplasia 76
Maldifferentiation (dysgenesis, dysplasia) 76
Ectopia, heterotopia and choristomas 76
Complex disorders of growth and morphogenesis 76
Neural tube defects 76
Disorders of sexual differentiation 76
Cleft palate and related disorders 77
Further reading 78
5 Responses to cellular injury 79
Cellular injury 80
Causative agents and processes 80
Physicochemical agents 80
Biological agents 81
Blockage of metabolic pathways 81
Cellular respiration 81
Glucose deprivation 81
Protein synthesis 81
Loss of growth factor or hormonal influence 81
Ischaemia and reperfusion injury 81
Free radicals 81
Failure of membrane integrity 82
DNA damage or loss 82
Patterns of cellular injury and death 83
Autophagy 83
Lethal cell injury 83
Necrosis 83
Coagulative necrosis 84
Colliquative necrosis 84
Caseous necrosis 84
Gangrene 84
Fibrinoid necrosis 84
Fat necrosis 85
Patterns of cell death in systematic pathology 85
Repair and regeneration 85
Cell renewal 85
Stem cells 85
Complete restitution 86
Organisation 86
Granulation tissue 86
Wound contraction and scarring 87
Outcome of injuries in different tissues 87
Skin 87
Incised wound: healing by first intention 87
Tissue loss: healing by second intention 87
Keloid nodules 87
Mechanism of skin healing and repair 88
Gastrointestinal tract 88
Mucosal erosions 88
Mucosal ulceration 88
Bone 89
Fracture healing 89
Problems with fracture healing 89
Liver 89
Kidney 90
Muscle 90
Neural tissue 90
Modifying influences 91
Age 91
Disorders of nutrition 91
Neoplastic disorders 91
Cushing’s syndrome and steroid therapy 91
Diabetes mellitus and immunosuppression 91
Vascular disturbance 91
Denervation 92
Injury due to ionising radiation 92
Definition and sources 92
Electromagnetic radiation 92
Particulate radiation 92
Ultraviolet light 92
Units of dose 92
Background radiation 93
Mode of action 93
Effects on tissues 93
Early effects 93
Late effects 94
Bone marrow 94
Intestine 94
Skin 94
Gonads 94
Lung and kidney 94
Whole body irradiation 95
Ionising radiation and tumours 95
Principles of radiation protection 96
Further reading 97
6 Disorders of metabolism and homeostasis 99
Inborn errors of metabolism 100
Disorders of carbohydrate metabolism 100
Disorders of amino acid metabolism 100
Phenylketonuria 100
Alkaptonuria 101
Homocystinuria 101
Storage disorders 101
Disorders of cell membrane transport 101
Channelopathies 101
Cystic fibrosis 101
Cystic fibrosis transmembrane conductance regulator (CFTR) 102
Clinicopathological features 102
Diagnosis 102
Treatment 102
Porphyrias 102
Clinicopathological features 103
Disorders of connective tissue metabolism 104
Osteogenesis imperfecta 104
Marfan’s syndrome 104
Acquired metabolic disorders 104
Gout 104
Aetiology 105
Clinicopathological features 105
Water homeostasis 105
Dehydration 105
Water excess 105
Oedema and serous effusions 106
Inflammatory oedema 106
Venous oedema 106
Lymphatic oedema 106
Hypoalbuminaemic oedema 107
Ascites and pleural effusions 107
Electrolyte homeostasis 108
Sodium and potassium homeostasis 108
Hypernatraemia 108
Hyponatraemia 108
Hyperkalaemia 108
Hypokalaemia 108
Calcium homeostasis 108
Hypercalcaemia 108
Hypocalcaemia 109
Acid–base homeostasis 109
Acidosis and alkalosis 109
Respiratory acidosis 109
Metabolic acidosis 109
Respiratory alkalosis 109
Metabolic alkalosis 109
Metabolic consequences of malnutrition 109
Protein–energy malnutrition 110
Malnutrition in children 110
Kwashiorkor 110
Marasmus 111
Cachexia 111
Vitamin deficiencies 111
Thiamine (B1) deficiency 111
Folate and vitamin B12 deficiency 111
Vitamin C deficiency 112
Vitamin D deficiency 112
Vitamin K deficiency 112
Obesity 113
Metabolic syndrome 113
Trace elements and disease 113
Aluminium 113
Copper 114
Iodine 114
Lead 114
Mercury 114
Tissue depositions 115
Calcification 115
Dystrophic calcification 115
‘Metastatic’ calcification 115
Amyloid 116
Classification 116
Systemic amyloidosis 116
Myeloma-associated amyloidosis 117
Reactive (secondary) amyloidosis 117
Senile amyloidosis 117
Haemodialysis-associated amyloidosis 118
Hereditary amyloidosis 118
Localised amyloidosis 118
Clinical effects and diagnosis 118
Further reading 119
7 Ischaemia, infarction and shock 121
Non-thromboembolic vascular insufficiency 122
Thromboembolic vascular occlusion 123
Clot 123
Thrombosis 123
Role of platelets 123
Thrombus formation 123
Arterial thrombosis 123
Venous thrombosis 124
Clinical effects 124
Fate of thrombi 125
Embolism 125
Pulmonary embolism 125
Systemic embolism 126
Embolic atheroma 127
Platelet emboli 127
Infective emboli 127
Fat embolism 127
Gas embolism 128
Amniotic embolism 128
Tumour embolism 128
Embolism of foreign matter 128
Infarction 128
Reperfusion injury 128
Morphology of infarcts 128
Gangrene 129
Capillary ischaemia 130
Susceptibility to ischaemia 130
Low-flow infarction 130
‘Watershed’ areas 130
Portal vasculature 130
Arterial stenoses 130
Infarction and metabolic activity 131
Shock 131
Cardiogenic shock 132
Hypovolaemic shock 132
Other vascular effects of bacterial toxaemia 132
Further reading 132
8 Immunology and immunopathology 133
Defence against infection 134
Non-specific defences 134
Innate immunity 134
Specific immunity 134
Key molecules 134
Antigens 134
Antibody 135
T-cell receptors 136
Major histocompatibility complex antigens 137
Accessory and co-stimulatory molecules 138
Cytokines 139
Structural organisation of the immune system 139
T- and B-lymphocyte development 140
Primary and secondary lymphoid organs 140
Functional organisation of the immune response 142
Antigen presentation 142
Antibody production 142
Cell-mediated responses 143
Non-specific effector mechanisms 143
Complement 143
Complement activation 143
Classical pathway activation 144
Alternative pathway activation 144
Lectin pathway activation 144
The membrane attack complex 144
Biological effects of complement 144
Control of the complement pathway 144
Macrophages 145
Neutrophil polymorphonuclear leucocytes 145
Antibody-dependent cell-mediated cytotoxicity 145
Natural killer cells 145
Outcomes of immune responses 145
Direct effects of antibody 146
Indirect effects of antibody 146
Killing of target cells 146
Inflammation 146
Immunodeficiency 146
Primary antibody deficiencies 146
Transient hypogammaglobulinaemia of infancy 147
X-linked agammaglobulinaemia (XLA) – Bruton’s disease 148
Hyper-IgM syndrome 148
Selective IgA deficiency 148
Common variable immunodeficiency 148
Primary defects in cell-mediated immunity 148
Severe combined immunodeficiency 148
DiGeorge syndrome (‘Catch 22’ anomaly) 148
Primary defects in phagocyte function 149
Chronic granulomatous disease 149
Primary complement deficiency 149
Secondary immunodeficiency 149
Acquired immune deficiency syndrome (AIDS) 150
Transmission of HIV 150
Clinical spectrum of HIV infection 151
Immunopathogenesis of HIV infection 151
Therapeutic options 151
Hypersensitivity reactions 152
Immediate hypersensitivity (type I) 152
Antibody to cell-bound antigen (type II) 153
Immune complex hypersensitivity (type III) 153
Delayed-type hypersensitivity (type IV) 154
Autoimmunity and autoimmune disease 156
Patterns of autoimmune disease 156
Organ-specific autoimmune diseases 156
Non-organ-specific autoimmune diseases 156
Epidemiology of autoimmune disease 157
Immunological tolerance 157
Thymic tolerance 157
Peripheral tolerance 157
Immunological ignorance 157
Anergy 157
Regulation and suppression 157
B-cell tolerance 158
Breakdown of tolerance 158
Overcoming peripheral tolerance 158
Molecular mimicry 158
Aetiology of autoimmune disease 158
Genetic factors 158
Environmental factors 158
Hormones 158
Infection 159
Drugs 159
Ultraviolet radiation 159
Mechanisms of tissue damage 159
Treatment of autoimmune diseases 159
Replacement of function 159
Suppression of the autoimmune response 159
Principles of organ transplantation 160
Histocompatibility genetics 160
Kidney transplantation 160
Selection of recipient and donor 160
The post-transplantation period 161
Clinical rejection 161
Immunopathology of graft rejection 161
Immunosuppression 161
Graft survival 162
Complications 162
Transplantation of other organs 162
Liver transplantation 162
Heart transplantation 163
Pancreatic transplantation 163
Skin grafting 163
Corneal grafting 163
Bone marrow transplantation 163
Selection and preparation of patients 163
Complications 163
Peripheral blood stem cell transplantation 164
Further reading 164
Websites 164
9 Inflammation 165
Acute inflammation 166
Causes of acute inflammation 166
Microbial infections 166
Hypersensitivity reactions 166
Physical agents 166
Irritant and corrosive chemicals 166
Tissue necrosis 166
Essential macroscopic appearances of acute inflammation 166
Redness (rubor) 166
Heat (calor) 166
Swelling (tumor) 167
Pain (dolor) 167
Loss of function 167
Early stages of acute inflammation 167
Changes in vessel calibre 167
Increased vascular permeability 167
Features of the fluid exudate 168
Ultrastructural basis of increased vascular permeability 168
Other causes of increased vascular permeability 168
Tissue sensitivity to chemical mediators 169
Formation of the cellular exudate 169
Margination of neutrophils 169
Adhesion of neutrophils 169
Neutrophil emigration 169
Diapedesis 169
Later stages of acute inflammation 170
Chemotaxis of neutrophils 170
Chemical mediators of acute inflammation 170
Chemical mediators released from cells 170
Plasma factors 170
Role of tissue macrophages 171
Role of the lymphatics 171
Role of the neutrophil polymorph 171
Movement 171
Adhesion to microorganisms 171
Phagocytosis 172
Intracellular killing of microorganisms 172
Release of lysosomal products 172
The role of mast cells 172
Special macroscopic appearances of acute inflammation 172
Effects of acute inflammation 172
Beneficial effects 172
Harmful effects 174
Sequelae of acute inflammation 174
Resolution 174
Suppuration 174
Abscess 175
Organisation 175
Progression to chronic inflammation 175
Systemic effects of inflammation 176
Pyrexia 176
Constitutional symptoms 176
Weight loss 176
Reactive hyperplasia of the reticuloendothelial system 176
Haematological changes 176
Amyloidosis 176
Chronic inflammation 177
Causes of chronic inflammation 177
Primary chronic inflammation 177
Transplant rejection 177
Progression from acute inflammation 177
Recurrent episodes of acute inflammation 177
Macroscopic appearances of chronic inflammation 178
Microscopic features of chronic inflammation 178
Paracrine stimulation of connective tissue proliferation 178
Cellular cooperation in chronic inflammation 178
Macrophages in chronic inflammation 179
Specialised forms of macrophages and granulomatous inflammation 179
Epithelioid histiocytes 179
Histiocytic giant cells 181
Langhans giant cells 181
Foreign body giant cells 181
Role of inflammation in systemic and organ-specific diseases 181
Further reading 182
10 Carcinogenesis and neoplasia 183
General characteristics of neoplasms (tumours) 184
Definitions 184
Incidence of tumours 184
Structure of tumours 184
Stroma 184
Tumour shape and correlation with behaviour 185
Tumour histology 185
Classification of tumours 186
Behavioural classification 186
Benign tumours 186
Malignant tumours 187
Histogenetic classification 188
Histological grade (degree of differentiation) 189
Nomenclature of tumours 189
Epithelial tumours 190
Benign epithelial tumours 190
Malignant epithelial tumours 190
Carcinoma in situ 190
Connective tissue and other mesenchymal tumours 191
Benign connective tissue and mesenchymal tumours 192
Malignant connective tissue and mesenchymal tumours 192
Eponymously named tumours 192
Miscellaneous tumours 192
Teratomas 192
Embryonal tumours: the ‘blastomas’ 192
Mixed tumours 192
Endocrine tumours 193
Hamartomas 193
Cysts 193
Biology of tumour cells 193
Aberrant proliferation and cellular immortalisation 194
Genomic instability in tumour cells 194
Mitotic and apoptotic activity 194
Metabolic and other abnormalities 194
Tumour products 194
Carcinogenesis 195
Identification of carcinogens 196
Epidemiological evidence 196
Occupational and behavioural risks 197
Scrotal carcinoma 197
Lung carcinoma 197
Carcinoma of the cervix 197
Bladder carcinoma 197
Direct evidence 197
Thorotrast 197
Thyroid carcinoma and radiation in children 197
Experimental testing 198
Known or suspected carcinogens 198
Chemical carcinogens 198
Polycyclic aromatic hydrocarbons 199
Aromatic amines 199
Nitrosamines 199
Azo dyes 199
Alkylating agents 200
Oncogenic viruses 200
Human papillomavirus 200
Epstein–Barr virus 200
Radiant energy 201
Ultraviolet light 201
Ionising radiation 202
Hormones 202
Bacteria, fungi, parasites and miscellaneous carcinogens 202
Bacteria 202
Fungi 202
Parasites 202
Miscellaneous: asbestos 202
Host factors in carcinogenesis 202
Race 203
Diet 203
Constitutional factors 203
Inherited predisposition 203
Age 203
Sex 203
Premalignant lesions and conditions 203
Transplacental carcinogenesis 204
Cellular and molecular events in carcinogenesis 205
Experimental observations 205
Latency 205
Initiation, promotion and progression 205
Genetic abnormalities in tumours 206
Chromosomal abnormalities 206
Genetic mechanisms in carcinogenesis 207
Genomic instability 207
Tumour suppressor genes 208
‘Caretakers’ and ‘gatekeepers’ 208
Oncogenes 209
Activation of oncogenes in tumours 210
Autocrine stimulation of neoplastic cell growth 211
Epigenetic contribution to tumour growth 211
Interaction of carcinogens with oncogenes and tumour suppressor genes 211
Behaviour of tumours 212
Invasion and metastasis 212
Invasion 213
Proteinases and inhibitors 213
Clinicopathological significance 214
Metastasis 214
The metastatic sequence 214
Routes of metastasis 215
Haematogenous metastasis 215
Lymphatic metastasis 215
Transcoelomic metastasis 215
Clinical effects of tumours 216
Local effects 216
Metabolic effects 216
Tumour type-specific effects 216
Non-specific metabolic effects 216
Prognosis 217
Prognostic indices 217
Tumour type 217
Tumour grade 217
Tumour stage 217
Tumour dormancy 218
Early detection of cancer by screening 218
Hallmarks 219
Further reading 219
Websites 219
11 Ageing and death 221
Ageing 222
3 Systematic Pathology 245
13 Cardiovascular system 246
Common clinical problems from cardiovascular disease 247
Diseases of the arteries and other vessels 248
Normal arterial structure 248
Age-related vascular changes 248
Atherosclerosis 249
Atherosclerotic lesions 249
What causes atherosclerosis? 250
How do lesions develop? 251
Clinical manifestations of atherosclerosis 252
Plaque morphology and the vulnerable plaque concept 252
Preventive and therapeutic approaches to atherosclerosis and atherothrombosis 253
Surgical and percutaneous interventions 253
Aneurysms 253
Atherosclerotic aortic aneurysms 253
Aortic dissection (dissecting aneurysms) 253
‘Berry’ aneurysms 254
Capillary microaneurysms 254
Vasculitic aneurysms 254
Mycotic aneurysms 255
Hypertension 255
Aetiological classification 255
Epidemiology 255
Essential hypertension 256
The sympathetic nervous system 256
The renin–angiotensin–aldosterone system 256
Dietary sodium and potassium 256
Secondary hypertension 257
Renal disease and hypertension 257
Endocrine causes 257
Coarctation of the aorta 257
Drug therapy 257
Pathological classification 257
Benign (essential) hypertension 257
Malignant hypertension 257
Pulmonary hypertension 258
Vascular and systemic effects 258
Vascular changes 258
Heart 258
Nervous system 259
Kidneys 259
Diabetic vascular disease 259
Vasculitis 259
Pathogenesis 259
Systemic vasculitis 259
Cutaneous small vessel vasculitis 260
Cranial (giant cell) arteritis 261
Pulseless (Takayasu’s) disease 261
Buerger’s disease 261
Diseases of veins 262
Normal venous structure 262
Venous thrombosis 262
Varicosities 262
Diseases of lymphatics 263
Normal lymphatic structure 263
Lymphatic involvement in disease 263
Tumours of blood vessels 263
Benign tumours 263
Malignant tumours 263
Cardiac disease 263
Normal structure and function of the heart 263
Heart failure 264
Pathophysiology 264
Ventricular function in heart failure 264
Neurohormonal changes in heart failure 265
Other pathophysiological changes in heart failure 265
Clinicopathological features 266
Dyspnoea 266
Systemic venous congestion and oedema 266
Other pathophysiological changes 266
Ischaemic heart disease 267
Pathophysiology 267
Myocardial infarction 267
Clinical features 267
Morphology 268
Serology 268
Clinical classification: STEMI versus non-STEMI 269
Complications 270
Unstable angina 270
Chronic ischaemic heart disease 270
Clinical features 270
Morphology 271
Sudden cardiac death 271
Aetiology 271
Prevention 272
Valvular heart disease 272
Pathophysiology 272
Clinicopathological features 273
Mitral incompetence 274
Mitral stenosis and rheumatic fever 274
Aortic stenosis 275
Aortic incompetence 275
Tricuspid and pulmonary valve disease 275
Infective endocarditis 275
Aetiology 275
Morphology 275
Endocarditis in unusual hosts 276
Patients with prosthetic heart valves 276
The elderly 276
Drug addicts 276
Complications 277
Local effects 277
Systemic effects 277
Diagnosis, treatment and prevention 277
Investigations 277
Treatment 278
Prevention 278
Non-infective endocarditis 278
Pericarditis and myocarditis 278
Pericarditis 278
Acute pericarditis 278
Chronic pericarditis 279
Glossary 721
Index 731
A 731
B 734
C 737
D 741
E 743
F 744
G 745
H 747
I 749
J 751
K 751
L 752
M 753
N 756
O 757
P 758
Q 761
R 761
S 762
T 765
U 767
V 767
W 768
X 769
Y 769
Z 769