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Pocket Essentials of Clinical Medicine

Pocket Essentials of Clinical Medicine

Anne Ballinger

(2011)

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Book Details

Abstract

Mini Kumar & Clark goes into its fifth edition! New to this best-selling, portable, quick reference to clinical medicine:

  • Fully updated in line with the latest edition of Kumar & Clark’s Clinical Medicine
  • New chapter on malignant disease
  • Practical procedures and therapeutics taken into individual chapters as appropriate.

From reviews of the previous edition:

‘This really is an excellent medical textbook … Easily covers undergraduate medicine.’

‘Pocket Essentials is a great little book to review the night before you start on a rotation. It is small enough that you can easily read over the chapter and then appear on the ward with a good idea of what is going on.’

‘In short this book is concise, succinct and gets straight to the point.’

‘This book summarises everything you need to know: causes, diagnoses and treatments.’

‘I am finding this book very helpful and more importantly very concise. It has most things you need to know about common clinical pathologies.’

‘… I turned to Pocket Essentials of Clinical Medicine as my clinical medicine reference guide – and what a guide! An excellent book, which gives you the clinical features, investigations and management for a whole variety of different illnesses. The book is clearly laid out, and even has normal blood chemistry values at the end. Do yourself a favour and buy this book!’

‘This mini paperback is a must for anyone studying medicine. It gives all the information one would need and all without the pain of carrying around a large book.’

‘I liked this book … it was useful having a smaller reference book … to carry around on wards etc. – it's more digestible and easier to follow than big K&C, and gives a little more background than the Oxford Handbook – and I know people who use it to revise for finals.’


Table of Contents

Section Title Page Action Price
Front cover cover
Medical emergencies ifc_2
Symptom based ifc_2
System based ifc_2
Infectious diseases and tropical medicine ifc_2
Gastroenterology and nutrition ifc_2
Liver, biliary tract and pancreatic disease ifc_2
Diseases of the blood and haematological malignancies ifc_2
Malignant disease ifc_2
Rheumatology ifc_2
Water and electrolytes ifc_2
Renal disease ifc_2
Cardiovascular disease ifc_2
Respiratory disease ifc_2
Intensive care medicine ifc_2
Poisoning, drug and alcohol abuse ifc_2
Endocrinology ifc_2
Diabetes mellitus and other disorders of metabolism ifc_2
The special senses ifc_2
Neurology ifc_2
Dermatology ifc_2
Half title page i
series page ii
Essentials of Kumar and Clark's Clinical Medicine, 5/e iii
Copyright page iv
Table of Contents v
Series Preface vii
Preface ix
Abbreviations xi
Significant websites xv
General Websites xv
Medical dictionaries xv
Guidelines and evidence based medicine xv
Medical calculators xvi
Healthcare journals and magazines xvi
Medical societies and organizations xvi
Others xvi
Chapter-Specific Websites xvi
1 Ethics and communication xvi
2 Infectious diseases xvii
3 Gastroenterology and nutrition xvii
1 Ethics and communication 1
Legally valid consent 2
Obtaining consent 2
Special circumstances 3
Emergencies 3
Adults who lack capacity to consent 3
Children 3
Research procedures 3
Teaching 4
Human immunodeficiency virus (HIV) testing 4
Advance directives 4
Communication 4
The medical interview 5
1. Building a relationship 5
2. Opening the discussion 5
3. Gathering information 5
4. Understanding the patient 6
5. Sharing information 6
6. Reaching agreement on management 6
7. Providing closing 6
Breaking bad news 6
Complaints and lawsuits 8
Culture and communication 8
Patients with impaired faculties for communication 8
Medical record keeping 9
2 Infectious diseases 11
Common investigations in infectious disease 12
Pyrexia of unknown origin 13
Investigations 13
Management 14
Septicaemia 15
Aetiology 15
Clinical features 15
Investigations 16
Management 16
Common viral infections 16
Measlesnd 16
Clinical features 16
The pre-eruptive and catarrhal stage 16
Eruptive or exanthematous stage 17
Complications 17
3 Gastroenterology and nutrition 65
Gastroenterology 65
Symptoms of gastrointestinal disease 65
Dyspepsia and indigestion 65
Dysphagia 65
Vomiting 65
Flatulence 66
Diarrhoea and constipation 66
Steatorrhoea 67
Abdominal pain 67
Investigation of gastrointestinal disease 67
Endoscopy 67
Oesophagogastroduodenoscopy (OGD, ‘gastroscopy’) 67
Sigmoidoscopy 68
Colonoscopy 68
Small bowel examination 69
Imaging 69
Plain X-rays 69
Ultrasound 69
Transabdominal ultrasound 69
Endoscopic ultrasound (EUS) 69
Endoanal and endorectal ultrasonography 69
Computed tomography (CT) scan 70
Magnetic resonance imaging (MRI) 71
Positron emission tomography (PET) scanning 71
Contrast studies 71
Oesophageal physiology testing 71
The mouth 71
Mouth ulcers 72
Non-infective 72
Infective 72
Oral white patches 72
Atrophic glossitis 72
Geographical tongue 72
Periodontal disorders 73
Salivary gland disorders 73
The oesophagus 73
Gastro-oesophageal reflux disease (GORD) 74
Pathophysiology 74
Clinical features 74
Investigations 74
OGD 74
24-hour intraluminal pH monitoring or impedance 74
Management 74
Complications 75
Oesophageal stricture formation 75
Barrett’s oesophagus, 75
Achalasia 76
Pathology 76
Clinical features 76
Investigations 76
Management 76
Complications 77
Systemic sclerosis 77
Other oesophageal dysmotility disorders 77
Hiatus hernia 77
Benign oesophageal strictures 77
Oesophageal perforation 78
Iatrogenic perforation 78
Traumatic or spontaneous oesophageal rupture 78
Malignant oesophageal tumours 78
Pathology 78
Epidemiology and aetiological factors 78
Squamous carcinoma 78
Adenocarcinoma 78
Clinical features 78
Investigations 79
Management 79
Prognosis 79
Benign oesophageal tumours 79
The stomach and duodenum 79
Helicobacter pylori infection 80
Epidemiology 80
Clinicopathological features 80
Diagnosis of infection 80
Management 80
Peptic ulcer disease 81
Epidemiology 81
Aetiology 81
Clinical features 82
Investigations 82
Management 82
Ulcers associated with H. pylori 82
H. pylori-negative peptic ulcers 83
Surgery 83
Complications 83
Perforation 83
Gastric outlet obstruction 83
Haemorrhage 83
Management of dyspepsia 83
Gastropathy and gastritis 83
Gastropathy 84
Gastritis 85
Gastric cancer 85
Epidemiology 85
Aetiology 85
Pathology 85
Clinical features 86
Investigations 86
Management 86
Prognosis 86
Other gastric tumours 86
GISTs 86
Gastric lymphoma 86
Gastric polyps 86
Gastrointestinal bleeding 87
Acute upper gastrointestinal bleeding 87
Aetiology 87
Management 87
Immediate management 87
Risk assessment 87
Resuscitate 87
Pre-endoscopy drug therapy 87
Determine site of bleeding 88
Specific management 89
Post-endoscopy 90
Lower gastrointestinal bleeding 91
Management 91
Specific management 91
Chronic gastrointestinal bleeding 91
Investigations 92
Management 92
The small intestine 92
Coeliac disease (gluten-sensitive enteropathy) 93
Aetiopathogenesis 93
Clinical features 93
Investigations 94
Serum antibodies 94
Distal duodenal biopsies 94
Blood count 94
Small bowel radiology or capsule endoscopy 94
Bone densitometry 94
Management 94
Complications 95
Dermatitis herpetiformis 95
Tropical sprue 95
Bacterial overgrowth 95
Clinical features 95
Diagnosis 96
Management 96
Intestinal resection 96
Whipple’s disease 96
Tuberculosis 97
Clinical features 97
Diagnosis 97
Imaging 97
Histology 97
Management 97
Protein-losing enteropathy 97
Meckel’s diverticulum 97
Intestinal ischaemia 98
Tumours of the small intestine 98
Malignant tumours 98
Benign small bowel tumours 98
Carcinoid tumours 98
Pathology 98
Clinical features 99
Investigations 99
Management 99
Inflammatory bowel disease 99
Epidemiology 99
Aetiology 99
Genetic susceptibility 99
Environment 100
Host immune response 100
Pathology 100
Clinical features 100
Crohn’s disease 100
Ulcerative colitis 100
Investigations 100
Blood tests 101
Radiology and imaging 101
Rigid or flexible sigmoidoscopy 101
Colonoscopy 102
Small bowel imaging 102
Perianal CD 102
Ultrasonography 102
Plain abdominal X-ray 102
Radiolabelled white cell scanning 102
Differential diagnosis 102
Management 103
Medical 103
Surgery 104
Cancer in inflammatory bowel disease 106
Prognosis 106
Microscopic colitis 106
The colon and rectum 106
Constipation 107
Investigation 107
Management 108
Faecal incontinence 108
Diverticular disease 108
Aetiology 109
Clinical features 109
Management 109
Miscellaneous conditions 109
Megacolon 109
Ischaemic colitis 109
Colon polyps and the polyposis syndromes 110
Adenomatous polyps 110
Colorectal cancer 110
Epidemiology 110
Inheritance 112
Pathology 112
Clinical features 112
Investigation 113
Colonic examination 113
Blood tests 113
Radiology 113
Faecal occult blood tests 113
Management 113
Prognosis 113
Screening 113
Diarrhoea 114
Acute diarrhoea 114
Chronic diarrhoea 114
Mechanisms of diarrhoea 114
Osmotic diarrhoea 114
Secretory diarrhoea 114
Inflammatory diarrhoea (mucosal destruction) 114
Motility related 115
Approach to the patient with diarrhoea 115
Step 1: 115
Step 2: 115
Step 3: 115
Investigation 115
Chronic diarrhoea 115
Functional bowel disorders 115
The acute abdomen 118
History 118
Examination 119
4 Liver, biliary tract and pancreatic disease 139
Liver biochemistry and liver function tests 140
Approach to interpretation of abnormal liver biochemistry 141
Other investigations in liver and biliary disease 141
Magnetic resonance imaging (MRI) 141
Endoscopic retrograde cholangiopancreatography (ERCP) 141
Percutaneous transhepatic cholangiopancreatography (PTC) 143
Liver biopsy 143
Assessment of liver fibrosis and cirrhosis 143
Symptoms and signs of liver disease 143
Jaundice 145
Haemolytic jaundice 145
Congenital hyperbilirubinaemia 145
Cholestatic jaundice 146
Investigations 147
Hepatitis 148
Acute hepatitis 148
Chronic hepatitis 149
Viral hepatitisnd 149
Hepatitis And 149
Epidemiology 149
Clinical features 150
Investigations 150
Differential diagnosis 152
Management 152
Prophylaxis 152
Hepatitis Bnd 152
Epidemiology 152
Viral structure 152
Acute HBV infection 153
Chronic HBV infection 154
Treatment of chronic infection: whom to treat 155
Antiviral agents 156
Hepatitis B and HIV co-infection 156
Prophylaxis 156
Hepatitis D (delta or δ agent)nd 157
Hepatitis Cnd 157
Epidemiology 157
Clinical features 157
Diagnosis 157
Management 158
Hepatitis End 158
Fulminant hepatic failure 158
Autoimmune hepatitis 158
Aetiology 159
Clinical features 159
Investigations 159
Treatment 160
Prognosis 160
Non-alcoholic fatty liver disease (NAFLD) 160
Clinical features 160
Investigations 160
Management 160
Cirrhosis 161
Aetiology 161
Pathology 161
Clinical features 161
Investigations 161
Severity 161
Aetiology 162
Further investigations 162
Management 162
Prognosis 162
Portal hypertension 162
Aetiology 163
Clinical features 164
Variceal haemorrhage 164
Management 164
Active bleeding 164
Prevention of recurrent variceal bleeding 165
Ascites 166
Aetiology 166
Clinical features 166
Investigations 166
Management 167
Diuretics 167
Paracentesis 167
Transjugular intrahepatic portosystemic shunt 167
Complications 167
Portosystemic encephalopathy 168
Pathophysiology 168
Clinical features 168
Differential diagnosis 168
Investigations 169
Management 169
Prognosis 169
Hepatorenal syndrome 169
Hepatopulmonary syndrome 169
Liver transplantation 170
Types of chronic liver disease and cirrhosis 170
Alcoholic cirrhosis 170
Primary biliary cirrhosis 170
Epidemiology 170
Aetiology 170
Clinical features 171
Investigations 171
Management 171
Prognosis 172
Secondary biliary cirrhosis 172
Hereditary haemochromatosis 172
Aetiology 172
Clinical features 172
Investigations 173
Management 173
Prognosis 174
Wilson’s disease (hepatolenticular degeneration) 174
α1-antitrypsin deficiency 174
Alcohol and the liver 174
Fatty change 175
Alcoholic hepatitis 175
Clinical features 175
Investigations 175
Management 176
Alcoholic cirrhosis 176
Primary sclerosing cholangitis 176
Budd–chiari syndrome 177
Aetiology 177
Clinical features 177
Investigations 177
Treatment 177
Liver abscess 178
Aetiology 178
Clinical features 178
Investigations 178
Management 178
Amoebic liver abscess 178
Pyogenic abscess 179
Liver disease in pregnancy 179
Liver tumours 179
Hepatocellular carcinoma (hepatoma) 179
Aetiology 179
Clinical features 179
Investigations 180
Management 180
Prognosis 180
Benign liver tumours 180
Gallstones 180
Pathophysiology 180
Clinical presentation 181
Biliary pain 181
Clinical features 181
Investigations 182
Management 182
Acute cholecystitis 182
Clinical features 182
Investigations 183
Management 183
Chronic cholecystitis 183
Acute cholangitis 183
Clinical features 183
Investigations 184
Management 184
Common bile duct stones (choledocholithiasis) 184
The pancreas 185
Pancreatitis 185
Acute pancreatitis 185
Pathogenesis 185
Clinical features 185
Investigation 186
Management 187
General supportive care 187
Therapies to reduce the severity or frequency of complications 188
Complications 188
Chronic pancreatitis 189
Clinical features 189
Investigations 189
Treatment 190
Carcinoma of the pancreas 190
Epidemiology 190
Aetiology 190
Clinical features 190
Investigations 190
Management 191
Prognosis 192
Cancer of the bile ducts 192
Neuroendocrine tumours of the pancreas 192
5 Haematological disease 193
Anaemia 193
Clinical features 194
Classification of anaemia (Table 5.2) 195
Microcytic anaemia 195
Iron deficiency 196
Causes of iron deficiency 197
Clinical features 197
Investigations 197
Differential diagnosis 198
Management 198
Anaemia of chronic disease 198
Sideroblastic anaemia 198
Macrocytic anaemia 198
Megaloblastic anaemia 199
Vitamin B12 deficiency 199
Pernicious anaemia 199
Epidemiology 199
Clinical features 200
Investigation of B12 deficiency 200
Differential diagnosis 201
Management 201
Folate deficiency 201
Clinical features 201
Investigations 202
Management 202
Prevention of neural tube defects with folic acid 202
Differential diagnosis 202
Anaemia caused by marrow failure (aplastic anaemia) 203
Aetiology 203
Clinical features 203
Investigations 204
Differential diagnosis 204
Management 204
Haemolytic anaemia 205
Inherited haemolytic anaemias 206
Membrane defects 206
Hereditary spherocytosis 206
Clinical features 207
Investigations 208
Management 208
Hereditary elliptocytosis 208
Haemoglobin abnormalities 208
Thalassaemia 208
β-Thalassaemia 209
Investigations 210
Management 210
α-Thalassaemia 210
Antenatal diagnosis of haemoglobin abnormalities 210
Sickle syndromes 210
Clinical features 211
Vaso-occlusion 211
Anaemia 211
Long-term problems 212
Investigations 212
Management 212
Sickle cell trait 213
Metabolic red cell disorders 213
Glucose-6-phosphate dehydrogenase deficiency 213
Acquired haemolytic anaemia 214
Autoimmune haemolytic anaemia 214
Clinical features 215
Investigation 215
Management 215
Clinical features 216
Investigation 216
Management 216
Drug-induced haemolysis 216
Non-immune haemolytic anaemia 216
Paroxysmal nocturnal haemoglobinuria 216
Mechanical haemolytic anaemia 217
Myeloproliferative disorders 217
Polycythaemia 217
Polycythaemia vera 218
Clinical features 218
Investigations 219
Management 219
Secondary polycythaemia 219
Essential thrombocythaemia 219
Myelofibrosis (myelosclerosis) 220
Clinical features 220
Investigations 220
Management 221
Myelodysplasia 221
The spleen 221
Hypersplenism 221
Splenectomy 222
Blood transfusion 222
Whole blood 223
Red cell concentrates 223
Platelet concentrates 223
Fresh frozen plasma 223
Cryoprecipitate 223
Factor VIII and IX concentrates 223
Albumin 223
Immunoglobulins 223
Blood groups 224
Procedure for blood transfusion 224
Complications of transfusing red blood cells 225
The white cell 226
Neutrophils 227
Neutrophil leucocytosis 227
Neutropenia 227
Monocytes 227
Eosinophils 227
Lymphocytes 227
Haemostasis and thrombosis 228
Haemostasis 228
Investigation of bleeding disorders 230
Platelet disorders 231
Immune thrombocytopenic purpura (ITP) 232
Investigation 232
Management 233
First-line therapy 233
Second-line therapy 233
Thrombotic thrombocytopenic purpura (TTP) 233
Inherited coagulation disorders 233
Haemophilia A 233
Clinical features 233
Investigations 234
Management 234
Complications 234
Haemophilia B (Christmas disease) 234
von Willebrand’s disease 234
6 Malignant disease 251
Diagnosis of malignancy 251
Investigations 252
Cancer treatment 253
Chemotherapy 253
Radiotherapy 253
Endocrine therapy 254
Biological therapy 254
Myeloablative therapy and haemopoietic stem cell transplantation 255
Oncological emergencies 255
Superior vena cava syndrome 255
Acute tumour lysis syndrome 255
The leukaemias 256
General classification 256
Aetiology 256
Genetic factors 256
Environmental factors 257
Acute leukaemia 257
Epidemiology 257
Clinical features 257
Investigations 257
Management 258
Supportive care 258
Treatment 258
Acute myeloid leukaemia 258
Acute promyelocytic leukaemia 259
Prognosis 259
Acute lymphoblastic leukaemia 259
Chronic myeloid leukaemia 260
7 Rheumatology 271
The normal joint 271
Musculoskeletal symptoms 271
Common investigations in musculoskeletal disease 273
Blood tests 273
Simple blood tests 273
Autoantibodies 273
Imaging 273
Plain X-rays 273
Bone scintigraphy (isotope bone scan) 274
Ultrasound 274
MRI 274
DXA 274
Arthroscopy 274
Synovial fluid analysis 274
Investigation of suspected muscle disease 274
Common regional musculoskeletal problems 274
Pain in the neck and shoulder 274
Elbow pain 275
Hip problems 275
The knee 275
Back pain 276
Lumbar back pain 276
Investigations 277
Management 277
Intervertebral disc disease 277
Acute disc disease 277
Clinical features 278
Investigations 278
Management 278
Chronic disc disease 279
Mechanical problems 279
Spondylolisthesis 279
Spinal stenosis 279
Neck pain 279
Osteoarthritis 280
Epidemiology 280
Pathology and pathogenesis 280
Clinical features 280
Differential diagnosis 281
Investigations 282
Management 282
Inflammatory arthritis 282
Rheumatoid arthritis 283
Epidemiology 283
Aetiology and pathogenesis 283
Pathology 283
Clinical features 284
Non-articular manifestations 284
Investigations 285
Differential diagnosis 285
Management 285
NSAIDs and coxibs 287
Corticosteroids 287
Disease-modifying anti-rheumatic drugs 287
Biological DMARDs 287
Prognosis 288
The seronegative spondyloarthropathies 289
Ankylosing spondylitis 289
Clinical features 289
Investigations 290
Management 291
Psoriatic arthritis 292
8 Water, electrolytes and acid–base balance 323
Water and electrolyte requirements 323
Body fluid compartments 323
Osmotic pressure 324
Distribution of extracellular fluid 324
Intravenous fluids in clinical practice 325
Regulation of body fluid homeostasis 328
Regulation of extracellular volume 328
Abnormalities of extracellular volume 329
Increased extracellular volume 329
Clinical features 329
Aetiology 329
Management 330
Decreased extracellular volume 330
Aetiology 330
Clinical features 330
Investigations 331
Management 331
Plasma osmolality and disorders of sodium regulation 332
Regulation of body water content 333
Hyponatraemia 333
Hyponatraemia resulting from salt loss (hypovolaemic hyponatraemia) 333
Clinical features 334
Management 335
Hyponatraemia resulting from water excess (dilutional hyponatraemia) 335
Aetiology 335
Clinical features 335
Investigation 335
Management 336
Central pontine myelinolysis 336
Hypernatraemia 337
Aetiology 337
Clinical features 337
Investigations 337
Management 337
Disorders of potassium regulation 338
Hypokalaemia 338
Aetiology 338
Clinical features 338
Management 338
Hyperkalaemia 340
Aetiology 340
Clinical features 340
Management 341
Disorders of magnesium regulation 341
Hypomagnesaemia 342
Aetiology 342
Clinical features 342
Management 343
Hypermagnesaemia 343
Disorders of acid–base balance 343
Respiratory acidosis 344
Respiratory alkalosis 344
Metabolic acidosis 345
Clinical features 345
Differential diagnosis (the anion gap) 345
Lactic acidosis 346
Diabetic ketoacidosis 346
Renal tubular acidosis 346
Uraemic acidosis 347
Metabolic alkalosis 347
Clinical features 348
Management 348
Therapeutics 348
Diuretics (Table 8.4) 348
Mechanism of action 348
Indications 348
Preparations and dose 348
Side-effects 348
9 Renal disease 353
Presenting features of renal disease 353
Dysuria 355
Polyuria and nocturia 355
Oliguria 355
Haematuria 356
Pain 356
Investigation of renal disease 356
Blood tests 356
Glomerular filtration rate 357
Calculation of creatinine clearance using the Cockroft–Gault equation 357
Men 357
Women 357
Urine dipstick testing 357
Proteinuria 357
Haematuria 358
Glycosuria 360
Urine microscopy 360
White cells 360
Red cells 361
Casts 361
Bacteria 361
Imaging techniques 361
Plain X-ray 361
Ultrasonography 361
CT 361
Magnetic resonance imaging (MRI) 362
Excretion urography 362
Renal arteriography (angiography) 362
Antegrade pyelography 362
Retrograde pyelography 362
Renal scintigraphy 362
Transcutaneous renal biopsy 362
Glomerular diseases 363
Normal glomerular structure 363
Pathogenesis and terms in glomerular disease 363
Classification and presentation of glomerulopathies 364
Nephrotic syndrome 365
Aetiology 365
Nephrotic syndrome with ‘bland’ urine sediments 365
Nephrotic syndrome with ‘active’ urine sediments (mixed nephrotic/nephritic) 366
Clinical features 367
Differential diagnoses 367
Investigations 367
Management 367
General oedema 367
Specific treatment 367
Complications 369
Acute glomerulonephritis (acute nephritic syndrome) 369
Clinical features 369
Investigations 370
Management 370
Rapidly progressive glomerulonephritis 370
Urinary tract infection 370
Pathogenesis 370
Clinical features 371
Natural history 371
Uncomplicated versus complicated infection 371
Acute pyelonephritis 372
Reflux nephropathy 372
Recurrent UTI 372
Investigations 372
Management 373
Antibiotics 373
A high fluid intake 373
Recurrent infection 373
UTI in pregnancy 373
Abacteriuric frequency or dysuria (‘urethral syndrome’) 373
Tuberculosis of the urinary tract 373
Tubulointerstitial nephritis 374
Acute tubulointerstitial nephritis (TIN) 374
Chronic tubulointerstitial nephritis 374
Hypertension and the kidney 374
Essential hypertension 375
Renal hypertension 375
Bilateral renal disease 375
Renovascular disease 375
Options for renal artery imaging 376
Management 377
Renal calculi and nephrocalcinosis 377
Aetiology 377
Calcium stones 377
Hypercalciuria 377
Hyperoxaluria 377
Uric acid stones 378
Infection-induced stones 378
Cystine stones 378
Clinical features 378
Differential diagnosis 379
Investigations 379
Management 379
Initial treatment 379
Prevention of recurrence 380
Nephrocalcinosis 381
Urinary tract obstruction 381
Aetiology 381
Clinical features 381
Investigations 382
Management 383
Acute renal failure/acute kidney injury 383
Definition 383
Classification 383
Prerenal failure 384
Management 385
Postrenal uraemia 385
Acute uraemia due to renal parenchymal disease 386
Clinical and biochemical features 386
Investigation of the uraemic emergency 387
Investigations 387
Management 388
Prognosis 388
Chronic kidney disease 388
Aetiology 389
Clinical features and investigations 390
Anaemia 390
Bone disease 390
Neurological 391
Cardiovascular disease 391
Other complications 392
Differentiating AKI from CKD 392
Management 393
Renoprotection 394
Reduce cardiovascular risk 394
Correction of complications 394
Hyperkalaemia 394
Calcium and phosphate 394
Anaemia 394
Acidosis 395
Infections 395
Referral to a nephrologist 395
Renal replacement therapy 395
Dialysis 395
Haemodialysis 396
Peritoneal dialysis 396
Haemofiltration 397
Complications of all long-term dialysis 397
Transplantation 397
Cystic renal disease 398
Solitary and multiple renal cysts 398
Autosomal-dominant polycystic kidney disease 398
Clinical features 398
Diagnosis 399
Management 399
Medullary sponge kidney 399
Tumours of the kidney and genitourinary tract 399
Renal cell carcinoma 399
Clinical features 399
Investigations 400
Management 400
Localized disease 400
Metastatic or locally advanced disease 400
Prognosis 400
Urothelial tumours 400
10 Cardiovascular disease 407
Common presenting symptoms of heart disease 407
Chest pain 407
Dyspnoea 407
Palpitations 407
Syncope 407
Other symptoms 409
Investigations in cardiac disease 409
The chest X-ray 409
The electrocardiogram 409
ECG waveform and definitions (Fig. 10.5) 411
Heart rate 411
Exercise electrocardiography 415
24-Hour ambulatory taped electrocardiography 417
Tilt testing 417
Echocardiography 417
Cardiac nuclear imaging 419
Cardiac computed tomography (CT) 419
Cardiovascular magnetic resonance (CMR) 419
Cardiac catheterization 420
Cardiac arrhythmias 420
General principles of management of arrhythmias 420
Sinus rhythms 421
Sinus arrhythmia 421
Bradycardia 421
Sinus bradycardia 421
Heart block 422
Atrioventricular block 422
First-degree AV block 422
Second-degree AV block 422
Third-degree AV block 422
Bundle branch block 423
Supraventricular tachycardias 425
Sinus tachycardia 425
Atrioventricular junctional tachycardias 425
Atrioventricular nodal re-entry tachycardia 425
Atrioventricular reciprocating tachycardia 427
Symptoms 427
Acute management 427
Long-term management 428
Atrial tachyarrhythmias 428
Atrial fibrillation (AF) 429
Management 429
Assessment for anticoagulation 430
Atrial flutter 430
Atrial ectopic beats 430
Ventricular tachyarrhythmias 431
Ventricular ectopic premature beats (extrasystoles) 431
Sustained ventricular tachycardia 431
Non-sustained ventricular tachycardia 431
Ventricular fibrillation (VF) 432
Long QT syndrome 432
Cardiac arrest 432
Prognosis 433
Heart failure 433
Aetiology 433
Pathophysiology 433
Activation of the sympathetic nervous system 433
Renin–angiotensin system 433
Natriuretic peptides 437
Ventricular dilatation 437
Ventricular remodelling 437
Clinical features 437
Symptoms 438
Signs 438
Investigations 438
Treatment of chronic heart failure 440
Drug treatment 440
Vasodilator therapy 440
β-blockers 440
Diuretics 441
Digoxin 442
Inotropes 442
Non-pharmacological treatment 442
Revascularization 442
Cardiac resynchronization therapy 442
Implantable cardioverter–defibrillator (ICD) 442
Cardiac transplantation 442
Prognosis 443
Acute heart failure 443
Clinical features 443
Management 443
Ischaemic heart disease 444
Irreversible risk factors for coronary artery disease 445
Age 445
Gender 445
Family history 445
Potentially changeable risk factors 445
Hyperlipidaemia 445
Cigarette smoking 445
Hypertension 445
Metabolic factors 445
Diets 445
Other risk factors 445
Estimation of cardiovascular risk 446
Angina 446
Clinical features 446
Diagnosis 446
Investigations 447
Management 447
Secondary prevention 447
Symptomatic treatment 448
Percutaneous coronary intervention (PCI) 448
Coronary artery bypass grafting 449
Acute coronary syndromes 449
Clinical features 449
Treatment 450
Risk stratification 450
ST segment elevation myocardial infarction (STEMI) 452
Clinical features 452
Investigations 452
The ECG 453
Cardiac markers 454
Other investigations 454
Management 454
Limitation of infarct size 454
Immediate primary angioplasty 454
Fibrinolytic agents 455
Subsequent management 456
Complications (Table 10.9) 456
Disturbances of rate, rhythm and conduction (p. 420) 456
Heart failure 457
Embolism 457
Pericarditis 458
Prognosis 458
Rheumatic fever 458
Epidemiology 458
Clinical features 458
Investigations 459
Blood count 459
Treatment 459
Chronic rheumatic heart disease 459
Valvular heart disease 459
Prosthetic heart valves 459
Mitral stenosis 460
Aetiology 460
Pathophysiology 460
Symptoms 460
Signs 460
Investigations 461
Chest X-ray 461
ECG 461
Echocardiography 461
Management 461
General 461
Specific 461
Mitral regurgitation 461
Aetiology 461
Pathophysiology 462
Symptoms 462
Signs 462
Investigations 462
11 Respiratory disease 505
Basic structure of the respiratory system 505
Function of the respiratory system 505
Symptoms of respiratory disease 506
Cough 506
Breathlessness 507
Wheezing 508
Haemoptysis 508
Chest pain (p. 407) 508
Investigation of respiratory disease 508
Sputum 508
Respiratory function tests 508
Peak expiratory flow rate (PEFR) 509
The spirometer 509
Arterial blood gas sampling 509
Walking distance 509
Imaging 509
Chest X-ray 509
Computed tomography (CT scan, p. 822) 510
Magnetic resonance imaging (MRI, p. 826) 511
Positron emission tomography (PET, p. 828) 511
Scintigraphic imaging 511
Pleural aspiration and biopsy 511
Bronchoscopy 512
Mediastinoscopy 512
Video-assisted thoracoscopic (VATS) lung biopsy 512
Smoking 512
Diseases of the upper respiratory tract 513
The common cold (acute coryza) 513
Rhinitis 513
Seasonal rhinitis 513
Perennial rhinitis 513
Diagnosis 513
Management 514
Acute pharyngitis 514
Acute laryngotracheobronchitis (croup) 514
Influenza 514
Clinical features 514
Diagnosis 515
Management 515
Complications 515
Prophylaxis 515
Inhalation of foreign bodies 515
Diseases of the lower respiratory tract 516
Acute bronchitis 516
Chronic obstructive pulmonary disease (COPD) 516
Epidemiology and aetiology 516
Pathophysiology 516
Pathogenesis 517
Clinical features 517
Complications 518
Investigations 519
Management 520
Cessation of smoking 520
Bronchodilators 520
Corticosteroids 520
Prevention of infection 520
Oxygen 520
Additional treatments 520
Acute exacerbation of COPD 521
Long term prognosis 522
Obstructive sleep apnoea (OSA) 522
Aetiology 522
Clinical features 522
Diagnosis 523
Management 523
Bronchiectasis 523
Aetiology 523
Clinical features 523
Investigations 524
Management 524
Complications 524
Cystic fibrosis 525
Clinical features 525
Investigations 525
Management 526
Prognosis 526
Asthma 526
Epidemiology 526
Classification 527
Aetiology 527
Pathogenesis 527
Inflammation 527
Remodelling 528
Precipitating factors 528
Clinical features 528
Investigations 529
Management 530
Avoidance of precipitating factors 530
Drug treatment 530
Acute severe asthma 532
Clinical features 532
Pneumonia 532
Clinical features 534
Investigations 535
Differential diagnosis 537
Management 537
Complications 537
Specific forms of pneumonia 537
Mycoplasma pneumoniae 537
Haemophilus influenzae 537
Chlamydia 537
Staphylococcus aureus 539
Legionella pneumophila 539
Pseudomonas aeruginosa 539
Pneumocystis jiroveci 540
Aspiration pneumonia 540
Complications of pneumonia: lung abscess and empyema 540
Clinical features 540
Investigations 540
Management 540
Tuberculosisnd 541
Epidemiology 541
Pathology 541
Clinical features 541
Investigations 543
Management 544
Prevention and chemoprophylaxis 545
Diffuse diseases of the lung parenchyma 546
Granulomatous lung disease 546
Sarcoidosis 547
Epidemiology 547
Immunopathology 547
Clinical features 547
Investigations 547
Differential diagnosis 548
Management 549
Prognosis 549
Granulomatous lung disease with vasculitis 549
Idiopathic interstitial pneumonias 550
Idiopathic pulmonary fibrosis (IFP) 550
Clinical features 550
Investigations 550
Differential diagnosis 550
Treatment 551
Prognosis 551
Hypersensensitivity pneumonitis 551
Clinical features 551
Investigations 551
Management 552
Other types of diffuse lung disease 552
Occupational lung disease 552
Coal worker’s pneumoconiosis 552
Asbestosis 553
Carcinoma of the lung 553
Epidemiology 553
Aetiology 553
Pathology 554
Clinical features 554
Local effects of tumour within a bronchus 554
Spread within the chest 555
Metastatic disease 555
Non-metastatic manifestations 555
Investigations 556
Confirm the diagnosis 556
Determine the histology 556
Assess spread of the tumour 557
Determine patient suitability for major operation 557
Treatment 557
Non-small-cell lung cancer 557
Small-cell lung cancer 557
Symptomatic treatments 557
Differential diagnosis 558
Metastatic tumours in the lung 558
Diseases of the chest wall and pleura 558
Rib fractures 558
Kyphosis and scoliosis of the spine 558
Pleurisy 558
Pleural effusion 559
Aetiology 560
Investigations 560
Diagnostic pleural fluid aspiration 560
Contrast-enhanced thoracic CT scan 561
Pleural biopsy 561
Management 561
Pneumothorax 561
Aetiology 561
Clinical features 562
Investigations 562
Management 562
Disorders of the diaphragm 563
Therapeutics 564
Bronchodilators 564
12 Intensive care medicine 571
Patient selection – withholding and withdrawing treatment 571
Critical care outreach and early warning systems 572
Acute disturbances of haemodynamic function (shock) 572
Pathophysiology 574
Sympathoadrenal 574
Neuroendocrine response 574
Release of mediators 574
Microcirculatory changes 575
Activation of the coagulation system 575
Progressive organ failure 575
Clinical features 575
Hypovolaemic shock 576
Cardiogenic shock 577
Mechanical shock 577
Anaphylactic shock 577
Sepsis 577
Management 578
Expansion of the circulating volume (preload) 578
Myocardial contractility and inotropic agents 579
Additional treatment 579
Specific treatment of the cause 581
Monitoring 581
Clinical 581
Invasive 581
Respiratory failure 582
Monitoring 582
Clinical 582
Pulse oximetry 583
Forced vital capacity (FVC) 583
Arterial blood gas analysis 583
Capnography 584
Management 584
Respiratory support 584
Acute lung injury/acute respiratory distress syndrome 586
Aetiology 586
Pathophysiology 586
Clinical features 587
Management 587
Prognosis 587
13 Drug therapy, poisoning, and alcohol misuse 589
Drug prescribing 589
Concordance with medication 589
Adverse drug reactions 590
Writing a prescription 590
Best practice for drug prescribing 591
Specific drugs 591
Drug poisoning 591
Clinical features 592
Investigations 592
Management 594
Emergency resuscitation (ABCDE, p. 740) 594
Prevention of further drug absorption 594
Antagonizing the effects of poisons 595
Psychiatric assessment 595
Specific drug problems 595
Aspirin 595
Clinical features 596
Investigations 597
Management 597
Paracetamol (acetaminophen) 597
Clinical features 597
Management 598
Other drugs 600
Carbon monoxide 601
Alcohol 601
Drug use 601
Opioids 601
Cannabis 602
Lysergide 602
Cocaine 602
Amfetamines 602
Solvents 603
Management of body packers 603
Alcohol use 603
Screening for problem drinking 604
Consequences of alcohol use and dependence 604
Physical complications 604
Alcohol withdrawal 605
14 Endocrine disease 607
Common presenting symptoms in endocrine disease 607
The hypothalamus and pituitary 609
Control and feedback 609
Pituitary space-occupying lesions and tumours 611
Underproduction 611
Overproduction 611
Local effects 612
Investigation 612
Hypopituitarism 613
Aetiology 613
Clinical features 614
Investigation 614
Management 614
Pituitary hypersecretion syndromes 615
Acromegaly and gigantism 615
Clinical features 615
Investigations 615
Management 616
Transsphenoidal surgical resection 617
Medical therapy 617
External radiotherapy 617
Hyperprolactinaemia 617
Aetiology 617
Clinical features 617
Investigations 618
Management 618
The thyroid axis 618
Assessment of thyroid function tests 619
Hypothyroidism 619
Aetiology 619
Autoimmune thyroiditis 620
Iatrogenic 620
Drug induced 620
Iodine deficiency 620
Congenital hypothyroidism 620
Clinical features 620
Investigations 620
Management 620
Borderline or subclinical hypothyroidism (compensated euthyroidism) 621
Myxoedema coma 622
Myxoedema madness 622
Hyperthyroidism 623
Graves’ disease 623
Toxic multinodular goitre 623
Solitary toxic nodule/adenoma 623
de Quervain’s thyroiditis 623
Postpartum thyroiditis 623
Clinical features 623
Investigations 623
Management 625
Antithyroid drugs 625
Radioactive iodine 625
Surgery 625
Thyroid crisis or ‘thyroid storm’ 626
Ophthalmic Graves’ disease 626
Aetiology 626
Clinical features 626
Investigations 626
Management 627
Goitre (thyroid enlargement) 627
Clinical features 627
Investigations 628
Management 629
Thyroid malignancy 629
Male reproduction and sex 629
Male hypogonadism 630
Klinefelter’s syndrome 630
Congenital deficiency of gonadotrophin-releasing hormone (GnRH) 631
Investigations 631
Management 631
Loss of libido and erectile dysfunction 631
Gynaecomastia 632
Female reproduction and sex 632
The menopause 632
Female hypogonadism and amenorrhoea 634
Aetiology 634
Investigations 635
Management 635
Hirsutism and polycystic ovary syndrome (PCOS) 635
Clinical features 636
Criteria for diagnosis 636
Investigations and differential diagnosis 636
Management 636
Local therapy for hirsutism 636
Systemic therapy for hirsutism 637
Treatment of menstrual disturbance 637
Treatment for infertility 637
The glucocorticoid axis 637
Addison’s disease: primary hypoadrenalism 637
Aetiology 638
Clinical features 638
Investigations 638
Management 639
Uses and problems of therapeutic steroid therapy 640
Secondary hypoadrenalism 641
Cushing’s syndrome 641
Clinical features 641
Investigations 643
Confirm raised cortisol 644
Establishing the cause of Cushing’s syndrome 644
Management 644
Incidental adrenal tumours 645
The thirst axis 645
Diabetes insipidus 645
Aetiology 645
Clinical features 646
Investigations 646
Management 646
Syndrome of inappropriate ADH secretion (SIADH) 647
Aetiology 647
Clinical features 647
Investigations 647
Management 648
Disorders of calcium metabolism 648
Hypercalcaemia 648
Aetiology 648
Primary hyperparathyroidism 649
Secondary hyperparathyroidism 649
Tertiary hyperparathyroidism 649
Clinical features 650
Investigations 650
Management 650
Treatment of primary hyperparathyroidism 651
Hypocalcaemia and hypoparathyroidism 651
Aetiology 651
Clinical features 651
Investigations 652
Management 653
Acute 653
Persistent hypocalcaemia 653
Disorders of phosphate concentration 653
Hypophosphataemia 654
Aetiology 654
Clinical features 654
Treatment 654
Oral phosphate supplements 654
Intravenous phosphate 655
Endocrinology of blood pressure control 655
The renin–angiotensin system 655
Aldosterone 657
Primary hyperaldosteronism 657
Clinical features 657
Investigations 657
Management 657
Phaeochromocytoma 657
Clinical features 658
Investigations 658
Management 658
Multiple endocrine neoplasia 658
Disorders of temperature regulation 659
Hypothermia 659
Aetiology 660
Clinical features 660
Diagnosis 660
Management 660
Hyperthermia (hyperpyrexia) 661
Therapeutics 662
Thyroid hormones 662
15 Diabetes mellitus and other disorders of metabolism 667
Diabetes mellitus 667
Glucose metabolism 667
Classification of diabetes 667
Aetiology and pathogenesis 669
Type 1 diabetes mellitus 669
Type 2 diabetes mellitus 669
Clinical features 669
Investigations 669
Impaired glucose tolerance 670
Management 670
Principles of treatment 671
Diet 671
Tablet treatments for type 2 diabetes 672
Insulin treatment 674
Complications of insulin therapy 675
Hypoglycaemia during insulin treatment 675
Whole pancreas and pancreatic islet transplantation 676
Measuring the metabolic control of diabetes 676
Home testing 676
Hospital (clinic) testing 676
Diabetic metabolic emergencies 677
Diabetic ketoacidosis 677
Pathogenesis 677
Clinical features 677
Investigations 677
Management 678
Hyperosmolar hyperglycaemic state 678
Clinical features 680
Management 680
Prognosis 680
Lactic acidosis 681
Complications of diabetes 681
Vascular 681
Macrovascular complications 681
Microvascular complications 681
Diabetic eye disease 681
Retinopathy 682
The diabetic kidney 684
Diabetic nephropathies 684
Ischaemic lesions 684
Infective lesions 684
Diabetic neuropathy 684
Symmetrical mainly sensory neuropathy 685
Acute painful neuropathy 685
Mononeuritis and mononeuritis multiplex (multiple mononeuropathy) 685
Diabetic amyotrophy 685
Autonomic neuropathy 686
The diabetic foot 686
Infections 686
The skin 686
Special situations 687
Surgery 687
Major surgery (i.e. having a general anaesthesic): 687
Minor surgery (e.g. endoscopy): 687
Insulin-treated patients 687
Tablet-controlled diabetes 688
Pregnancy and diabetes 688
Acutely ill hospital inpatients 688
Unstable diabetes 688
Hypoglycaemia in the non-diabetic 688
Insulinomas 688
Clinical features 690
Investigations 690
Treatment 690
Disorders of lipid metabolism 690
Measurement of plasma lipids 691
The primary hyperlipidaemias 692
Disorders of VLDL and chylomicrons – hypertriglyceridaemia alone 692
Disorders of LDL – hypercholesterolaemia alone 692
Combined hyperlipidaemia (hypercholesterolaemia and hyperlipidaemia) 693
Management of hyperlipidaemia 693
Guidelines to therapy 693
Lipid-lowering diet 693
Lipid-lowering drugs (Table 15.12) 693
Whom to treat 694
Primary prevention for people at risk of cardiovascular disease 694
Secondary prevention 695
Aims of treatment 695
The porphyrias 695
Acute intermittent porphyria 695
Clinical features 695
Investigations 696
Management 697
Other porphyrias 697
Amyloidosis 697
Therapeutics 697
Oral antidiabetic drugs 697
Mechanism of action 697
Indications 698
Preparations and dose 698
Metformin 698
Side-effects 698
16 The special senses 703
The ear 703
Hearing loss 703
Vertigo 704
Benign paroxysmal positional vertigo 704
Vestibular neuronitis 705
Ménière’s disease 705
Central causes 705
Ear infections 705
The nose and nasal cavity 706
Epistaxis (nose bleeds) 707
Sinusitis 707
The throat 707
Hoarseness (dysphonia) 707
Stridor 708
Sore throat 708
The eye 708
The red eye 708
Visual loss 709
17 Neurology 715
Common neurological symptoms 715
Headache 715
Dizziness, faints and ‘funny turns’ 715
Dizziness and syncope 717
Investigation 718
Weakness 718
The corticospinal tracts 718
The upper motor neurone 718
The lower motor neurone 720
Numbness 721
The sensory system 721
Peripheral nerve lesions 721
Spinal root lesions 721
Spinal cord lesions 721
Pontine lesions 724
Thalamic lesions 724
Cortical lesions 724
Tremor 724
Coordination of movement 724
The cerebellum 724
The cranial nerves 725
The olfactory nerve (first cranial nerve) 725
The optic nerve (second cranial nerve) and the visual system 726
Visual field defects 726
Optic nerve lesions 728
Defects of the optic chiasm 729
Defects of the optic tract and radiation 729
Defects of the occipital cortex 729
Optic disc oedema (papilloedema) and optic atrophy 729
Papilloedema 729
Optic atrophy 729
The pupils 729
Cranial nerves III–XII 730
The ocular movements and the third, fourth and sixth cranial nerves 731
The trigeminal nerve (fifth cranial nerve) 732
Trigeminal neuralgia 733
Clinical features 733
Management 733
Differential diagnosis 734
The facial nerve (seventh cranial nerve) 734
Lower motor neurone (LMN) lesions 734
Bell’s palsy 734
Clinical features 734
Investigations 734
Management 735
Prognosis 735
Ramsay Hunt syndrome 735
Upper motor neurone (UMN) lesions 735
The vestibulocochlear nerve (eighth cranial nerve) 735
Vertigo 736
Nystagmus 736
Pendular nystagmus 736
Jerk nystagmus 736
Glossopharyngeal, vagus, accessory and hypoglossal nerves (ninth to twelfth cranial nerves) 736
Common investigations in neurological disease 737
Blood tests 737
Imaging 737
Skull and spinal X-rays 737
Computed tomography (CT) 737
Magnetic resonance imaging (MRI) 737
Positron emission tomography (PET) 737
Doppler studies 737
Electroencephalography (EEG) 737
Lumbar puncture and cerebrospinal fluid (CSF) examination 737
Electromyography (EMG) 738
Investigation of suspected muscle disease 738
Unconsciousness and coma 738
Aetiology 739
Assessment 740
Immediate assessment 740
Further assessment 741
Investigations 741
Blood and urine tests 742
Radiology 742
CSF examination 742
Management 742
Prognosis 742
Brain death 742
Stroke and cerebrovascular disease 743
Definitions 743
Stroke 743
Stroke in evolution 743
A minor stroke 743
Transient ischaemic attack 743
Pathophysiology 743
Completed stroke 743
Transient ischaemic attacks 744
Risk factors 744
Transient ischaemic attacks (TIAs) 744
Investigations 745
Blood 745
Brain imaging 745
Carotid artery imaging 745
Treatment 745
Antithrombotic treatment 745
Other secondary prevention 746
Carotid endarterectomy 746
Cerebral infarction 746
Clinical features 746
Cerebral hemisphere infarcts 746
Brainstem infarction 746
Multi-infarct dementia 748
Management 748
Prognosis 750
Primary intracranial haemorrhage 750
Intracerebral haemorrhage 750
Subarachnoid haemorrhage (SAH) 750
Incidence 750
Aetiology 750
Clinical features 751
Investigation 752
Management 752
Prognosis 752
Subdural haematoma (SDH) 752
Extradural haemorrhage 753
Epilepsy and loss of consciousness 753
Epilepsy 753
Classification 753
Aetiology and precipitants 754
Evaluation and investigation 755
Management 755
Emergency measures 755
Status epilepticus 755
Antiepileptic drugs (AEDs) 756
Drug withdrawal 757
Neurosurgical treatment 757
Advice to patients 758
Movement disorders 758
Akinetic–rigid syndromes 759
Idiopathic Parkinson’s disease 759
Aetiology 759
Clinical features 759
Investigations 760
Management 760
Levodopa 760
Dopamine agonists 760
Monoamine oxidase B inhibitor 760
Additional treatment 760
Other akinetic-rigid syndromes 761
Drug-induced parkinsonism 761
‘Parkinsonism plus’ 761
Dyskinesias 761
Benign essential tremor 761
Chorea 761
Huntington’s disease 761
Hemiballismus 762
Myoclonus 762
Tics 762
Dystonias 762
Multiple sclerosis (MS) 763
Epidemiology 763
Aetiology 763
Pathology 763
Clinical features 763
Optic neuropathy 764
Brainstem demyelination 764
Spinal cord lesions 764
Differential diagnosis 764
Investigations 764
Management 765
Nervous system infection and inflammation 765
Meningitisnd 765
Clinical features 765
Acute bacterial meningitis 765
Viral meningitis 766
Chronic meningitis 766
Differential diagnosis 766
Management 767
Notification 767
Meningococcal prophylaxis 768
Encephalitis 768
Acute viral encephalitis 768
18 Dermatology 803
Introduction 803
Skin and soft tissue infections 803
Cellulitis and erysipelas 803
Clinical features 804
Diagnosis 804
Treatment 804
Necrotizing fasciitis 805
Gas gangrene 805
Fungal infections 805
Candida albicans 806
Common skin conditions 806
Acne vulgaris 806
Clinical features 807
Management 807
First-line therapy 807
Second-line therapy 807
Third-line therapy 807
Psoriasis 807
Aetiology 808
Clinical features 808
Associated features 809
Management 809
Topical treatment 809
Phototherapy 809
Systemic therapy 809
Urticaria/angio-oedema 809
Dictionary of terms 819
Index 831
A 831
B 834
C 836
D 840
E 842
F 843
G 844
H 845
I 848
J 850
K 850
L 850
M 852
N 854
O 856
P 856
Q 860
R 860
S 861
T 864
U 866
V 867
W 868
X 868
Y 869
Z 869
Normal values ibc_4