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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2683_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Series Editors’ foreword
- •Prefaces
- •Acknowledgements
- •Series Editors’ acknowledgements
- •History of the presenting complaint (HPC)
- •Past medical history (PMH)
- •Medications and allergies (DHX)
- •Family history (FHX)
- •Social history (SHX)
- •Systems review (SR)
- •General symptoms
- •Fatigue
- •Appetite
- •Weight change
- •Sweats
- •Pruritus (itching)
- •Sleep pattern
- •Cardiovascular symptoms
- •Chest pain
- •Shortness of breath (dyspnoea) and exercise tolerance
- •Loss of consciousness (syncope)
- •Palpitations
- •Ankle and calf swelling
- •Calf, thigh or buttock pain on exertion (claudication)
- •Respiratory symptoms
- •Dyspnoea
- •Cough
- •Sputum
- •Chest pain
- •Wheeze
- •Hoarse voice
- •Gastrointestinal disease
- •Abdominal pain
- •Dysphagia
- •Nausea and vomiting
- •Indigestion
- •Change in bowel habit or stools
- •Jaundice and itch
- •Abdominal swelling
- •Genitourinary symptoms
- •Dysuria
- •Change in urine appearance
- •Frequency and nocturia
- •Hesitancy
- •Contents
- •Loin pain
- •Incontinence
- •Menstruation
- •Discharge
- •Neurological symptoms
- •Headache
- •Dizziness and vertigo
- •Loss of consciousness
- •Visual disturbance
- •Altered hearing
- •General principles
- •Altered smell
- •Speech disturbance
- •Limb weakness, paraesthesiae and sensory loss
- •Metabolic and endocrine symptoms
- •Musculoskeletal symptoms
- •Pain
- •Weakness
- •Overview
- •The history
- •Presenting complaint (PC)
- •Visual survey
- •Position
- •Hands
- •Radial pulse
- •Blood pressure
- •Brachial and carotid artery
- •Jugular Venous Pressure
- •Face
- •Praecordium
- •Apex beat
- •Palpation
- •Auscultation
- •Summary
- •The respiratory system
- •Visual survey
- •Stiffness
- •Joint swelling
- •Disability
- •Skin symptoms
- •Rash
- •Pruritus
- •Precipitants
- •Haematological symptoms
- •Fatigue
- •Excessive bleeding or bruising
- •Recurrent infections
- •Glandular swelling
- •Conclusion of history taking
- •2 Clinical examination
- •ABCDE approach
- •Massive Blood Loss Protocol
- •General principles
- •Visual survey
- •Patient position, general behaviour and around the bed
- •Pallor
- •Cyanosis
- •Jaundice
- •Fluid status
- •Pigmentation
- •The face and body habitus
- •The hands
- •Hands
- •Nails
- •Tendons
- •Joints
- •Neuromuscular
- •Miscellaneous
- •The cardiovascular system
- •Position
- •Hands
- •Pulse
- •Blood pressure
- •Jugular venous pressure
- •Face and mouth
- •Trachea
- •Thorax
- •Inspection
- •Expansion
- •Tactile fremitus and vocal fremitus
- •Percussion
- •Auscultation
- •Summary
- •The abdomen
- •Visual survey
- •Position
- •Hands
- •Arms
- •Face and mouth
- •Neck
- •Trunk and back
- •Abdomen
- •Inspection
- •Palpation
- •Percussion
- •Auscultation
- •Concluding your examination
- •The nervous system
- •Visual survey
- •Cranial nerves
- •Cranial nerve I (olfactory nerve)
- •Cranial nerve II (optic nerve)
- •Cranial nerves III, IV and VI and eye movements
- •Cranial nerve III (oculomotor nerve)
- •Cranial nerve IV (trochlear nerve)
- •Cranial nerve VI (abducens nerve)
- •Cranial nerve V (trigeminal nerve)
- •Cranial nerve VII (facial nerve)
- •Cranial nerve VIII (vestibulocochlear nerve)
- •Cranial nerve IX (glossopharyngeal nerve)
- •Cranial nerve X (vagus nerve)
- •Cranial nerve XI (accessory nerve)
- •Cranial nerve XII (hypoglossal nerve)
- •Upper limb
- •Visual survey
- •Tone
- •Power
- •Coordination
- •Reflexes
- •Sensation
- •Lower limb
- •Visual survey
- •Tone
- •Power
- •Coordination
- •Reflexes
- •Sensation
- •Gait
- •Musculoskeletal examination
- •Visual survey
- •Look
- •Feel
- •Move
- •Assessment of disability
- •Hands
- •Skin and lymphadenopathy
- •Breast examination
- •Neck examination
- •3 Writing in the medical notes
- •General principles
- •Sample clerking
- •4 Chest pain
- •Introduction
- •History and examination findings
- •History
- •Type of chest pain
- •Onset and progression
- •Site and radiation
- •Nature of pain
- •Associated symptoms
- •Examination
- •Investigations
- •5 Shortness of breath
- •Introduction
- •History and examination findings
- •History
- •Onset
- •Severity
- •Precipitating and aggravating factors
- •Associated features
- •Other factors
- •Examination
- •Inspection
- •Palpation
- •Percussion
- •Auscultation
- •Investigations
- •Acute presentation
- •Chronic presentation
- •6 Cough and haemoptysis
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside
- •Blood tests
- •Imaging
- •Further investigations
- •7 Palpitations
- •Introduction
- •History and examination findings
- •History
- •Causes and contributing factors
- •Examination
- •Investigations
- •8 Pyrexia of unknown origin
- •Introduction
- •History and examination findings
- •Investigations
- •Bedside investigations
- •Blood tests
- •Microbiology tests
- •Further investigations
- •Differential diagnosis
- •9 Abdominal pain
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Ascertaining the underlying causes of abdomnal pain
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Further investigations
- •10 Heartburn and indigestion
- •Introduction
- •History and examination findings
- •Investigations
- •Common investigations
- •Specialized investigations
- •11 Gastrointestinal bleed
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Further investigations
- •12 Change in bowel habit
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Noninvasive
- •Invasive
- •Further investigations
- •13 Weight loss
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Blood tests
- •Imaging
- •14 Jaundice
- •Introduction
- •History and examination
- •History
- •Examination
- •Investigations
- •Haemolysis screen
- •Hepatocellular screen
- •Introduction
- •Micturition disturbances
- •History and examination findings
- •Examination
- •General appearance
- •Cardiovascular system
- •Abdominal examination
- •Neurological examination
- •Investigations
- •Urine tests
- •Blood tests
- •Imaging
- •Further investigations
- •Haematuria
- •History and examination findings
- •Initial tests
- •Imaging
- •Other investigations
- •Proteinuria
- •16 Headache and facial pain
- •Introduction
- •History and examination findings
- •History
- •Solitary acute episode
- •Progressive headache
- •Recurrent episodic headache and facial pain
- •Chronic headache and facial pain
- •Examination
- •Investigations
- •Blood tests
- •Imaging
- •Introduction
- •History and examination findings
- •Investigations
- •Imaging
- •Further investigations
- •Differential diagnosis
- •Thyroid disease
- •Hypothyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Blood tests
- •Other
- •Imaging
- •Hyperthyroidism
- •Aetiology
- •Primary hyperthyroidism
- •Clinical features
- •Investigations
- •Subacute (de Quervain) thyroiditis
- •Thyroid malignancy
- •Papillary thyroid carcinoma
- •Follicular thyroid carcinoma
- •Anaplastic carcinoma
- •Medullary thyroid carcinoma
- •Primary thyroid lymphoma
- •Further reading
- •18 Loss of consciousness
- •Introduction
- •History and examination findings
- •History
- •Before the event
- •The event itself
- •After the event
- •Risk factors
- •Examination
- •Comatose patient
- •Patient with blackouts
- •Investigations
- •19 Confusion and delirium
- •Introduction
- •History and examination findings
- •History
- •Pattern of confusion
- •Underlying causes
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Further tests
- •20 Stroke and TIA
- •Introduction
- •Causes and pathophysiology
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Further investigations
- •Management
- •Acute treatment
- •Prevention
- •21 Lumps
- •Introduction
- •History and examination findings
- •Investigations
- •Differential diagnosis
- •Localized lymphadenopathy
- •Generalized lymphadenopathy
- •Splenomegaly
- •22 Focal neurological deficits
- •Introduction
- •History and examination findings
- •History
- •Pattern of deficit
- •Onset
- •Precipitants
- •Progression
- •Evidence of cause
- •Examination
- •The anatomical site of the lesion
- •The underlying cause
- •The resultant disability
- •Investigations
- •Bedside investigations
- •Blood tests
- •Cerebrospinal fluid analysis
- •Imaging
- •Further investigations
- •23 Dizziness and vertigo
- •Introduction
- •History and examination findings
- •History
- •Onset and pattern of vertigo
- •Aural symptoms
- •Neurological symptoms
- •Examination
- •Investigations
- •24 Back pain and joint pain
- •Introduction
- •History and examination findings
- •History
- •Ask about associated features:
- •Other important points to consider include:
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Differential diagnosis
- •Joint disease
- •Back pain
- •25 Skin lesions and rash
- •Introduction
- •History and examination
- •History
- •Examination
- •Investigations
- •Differential diagnosis
- •Pigmented lesions
- •Scaly lesions
- •Vesicular lesions
- •Weepy or pustular lesions
- •Figurate erythema
- •Bullous lesions
- •Papular and nodular lesions
- •Photodermatoses
- •Maculopapular lesions
- •Ulcerated lesions
- •Petechial and purpuric lesions
- •Miscellaneous lesions
- •Introduction
- •History and examination findings
- •Investigations
- •Differential diagnosis
- •Platelet abnormality
- •Thrombocytopenia
- •Platelet dysfunction
- •Coagulation abnormality
- •Vitamin K deficiency
- •Factor deficiency
- •Acquired factor inhibitors
- •Vessel wall abnormalities
- •Hereditary
- •Acquired
- •27 Cardiovascular system
- •Coronary heart disease
- •General overview
- •Risk factors
- •Nonmodifiable risk factors
- •Family history
- •Ethnicity
- •Modifiable risk factors
- •Smoking
- •Poor nutrition
- •Hyperlipidaemia
- •Hypertension
- •Diabetes mellitus
- •Obesity
- •Pathophysiology
- •Clinical features
- •Investigations
- •Electrocardiogram
- •Exercise tolerance test
- •Echocardiography
- •CT coronary angiography
- •Nuclear imaging
- •Coronary angiography
- •Treatment
- •Lifestyle changes
- •Drug agents
- •Antiplatelet drugs
- •Nitrates
- •β-Blockers
- •Calcium channel blockers
- •Potassium channel activators
- •Angiotensin-converting enzyme inhibitors
- •Lipid-lowering drugs
- •Revascularization
- •Acute coronary syndrome
- •ST elevation myocardial infarction
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Acute management
- •Non-ST elevation myocardial infarction and unstable angina
- •General overview
- •Clinical features
- •Investigations
- •Risk scoring
- •Management
- •Acute management
- •Subsequent inpatient management of patients with acute coronary syndrome
- •Complications of myocardial infarction
- •Cardiac failure and cardiogenic shock
- •Cardiac rupture
- •Mitral regurgitation
- •Arrhythmias and conduction disturbances
- •Supraventricular arrhythmias
- •Arrhythmias
- •General overview
- •Investigations
- •Sinus tachycardia
- •Atrial fibrillation
- •Aetiology and pathophysiology
- •Complications
- •Management
- •Atrial flutter
- •Paroxysmal supraventricular tachycardia
- •Atrioventricular reentry tachycardia
- •Atrioventricular nodal reentry tachycardia
- •Management
- •Ventricular tachycardia
- •Torsades de pointes
- •Ventricular fibrillation
- •Bradycardias
- •Sinus bradycardia
- •Sick sinus syndrome
- •Heart block
- •Antiarrhythmic drugs
- •Supraventricular arrhythmias only
- •Supraventricular and ventricular arrhythmias
- •Ventricular arrhythmias
- •Heart failure
- •General overview
- •Aetiology
- •Clinical features
- •Left-sided heart failure
- •Right-sided heart failure
- •Congestive cardiac failure
- •Investigations
- •Blood tests
- •Imaging
- •Other
- •Management of acute heart failure
- •Management of chronic heart failure
- •Drug treatment
- •Angiotensin-converting enzyme inhibitors
- •β-Blockers
- •Diuretics
- •Aldosterone antagonists
- •Hydralazine in combination with a nitrate
- •Digoxin
- •Ivabradine
- •Nondrug therapy
- •Implantable cardioverter defibrillator and cardiac resynchronization therapy
- •Left ventricular assist devices
- •Transplantation
- •Hypertension
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Drug treatment
- •Angiotensin-converting enzyme inhibitors
- •Angiotensin II receptor blockers
- •Calcium channel blockers
- •Thiazide diuretics
- •β-Blockers
- •α-Adrenergic receptor blockers
- •Central acting agents
- •Vasodilators
- •Management of hypertension in pregnancy
- •Malignant (accelerated) hypertension
- •Valvular heart disease
- •General overview
- •Mitral stenosis
- •Clinical features
- •Management
- •Mitral regurgitation
- •Clinical features
- •Management
- •Mitral valve prolapse
- •Aortic stenosis
- •Clinical features
- •Management
- •Aortic regurgitation
- •Clinical features
- •Management
- •Tricuspid regurgitation
- •Pulmonary valve lesions
- •Miscellaneous conditions
- •Pericarditis and pericardial effusion
- •Clinical features
- •Management
- •Constrictive pericarditis
- •Cardiomyopathy
- •Hypertrophic obstructive cardiomyopathy
- •Dilated cardiomyopathy
- •Restrictive/infiltrative cardiomyopathy
- •Arrhythmogenic right ventricular dysplasia
- •Infective endocarditis
- •Clinical features
- •Management
- •Rheumatic fever
- •Major Jones criteria
- •Carditis (40%–50%)
- •Polyarthritis (80%)
- •Sydenham chorea (10%)
- •Erythema marginatum (5%)
- •Subcutaneous nodules (rare)
- •Management
- •Atrial myxomata
- •Congenital heart disease in adults
- •Acyanotic conditions
- •Atrial septal defect
- •Ventricular septal defect
- •Patent ductus arteriosus
- •Aortic coarctation
- •Aortic and pulmonary stenosis
- •Cyanotic conditions
- •Tetralogy of Fallot
- •Further reading
- •28 Respiratory system
- •Respiratory failure
- •General overview
- •Type I respiratory failure
- •Causes
- •Management
- •Type II respiratory failure
- •Causes
- •Management
- •Asthma
- •General overview
- •Aetiology
- •Pathophysiology
- •Clinical features
- •Investigations
- •Management
- •Emergency management
- •Long-term management
- •Chronic obstructive pulmonary disease
- •General overview
- •Aetiology
- •Cigarette smoking
- •α1-Antitrypsin deficiency
- •Occupation
- •Pathophysiology
- •Clinical features
- •Investigations
- •Management
- •Short-term management
- •Long-term management
- •Bronchiectasis
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Pneumonia
- •General overview
- •Aetiology
- •Community-acquired pneumonia
- •Atypical pneumonia
- •Hospital-acquired pneumonia (nosocomial)
- •Aspiration pneumonia
- •Opportunistic pneumonia
- •Clinical features
- •Typical
- •Atypical
- •Investigations
- •Bedside
- •Imaging
- •Other tests
- •CURB65 score
- •Management
- •Pulmonary embolism
- •Clinical features
- •Investigations
- •Management
- •Lung cancer
- •General overview
- •Aetiology
- •Pathology
- •Clinical features
- •Paraneoplastic syndrome
- •Investigations
- •Tumour, Node, Metastasis (TNM) staging
- •Management
- •Tuberculosis
- •General overview
- •Pathogenesis
- •Pulmonary tuberculosis
- •Extrapulmonary tuberculosis
- •Clinical features
- •Systemic
- •Pulmonary
- •Extrapulmonary
- •Investigations
- •Management
- •Pneumothorax
- •General overview
- •Clinical features
- •Management
- •Pleural effusion
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Interstitial lung disease
- •General overview
- •Aetiology
- •Known cause:
- •Unknown cause:
- •Clinical features
- •Investigations
- •Management
- •Idiopathic pulmonary fibrosis
- •Sarcoidosis
- •Occupational lung disease
- •Aspergillus and the lung
- •Hypoventilation syndromes and sleep-related respiratory disorders
- •General overview
- •Obstructive sleep apnoea syndrome
- •Obesity hypoventilation syndrome
- •Congenital hypoventilation syndrome
- •Acute respiratory distress syndrome
- •General overview
- •Management
- •Cystic fibrosis
- •General overview
- •Clinical features
- •Management
- •Further Reading
- •Upper gastrointestinal tract
- •Oesophageal disorders
- •Gastro-oesophageal reflux disease
- •Clinical features
- •Investigations
- •Management
- •Complications
- •Hiatus hernia
- •Sliding hiatus hernia
- •Rolling (or paraoesophageal) hiatus hernia
- •Barrett oesophagus
- •Eosinophilic oesophagitis
- •Oesophageal motility disorders
- •Achalasia
- •Oesophageal cancer
- •Clinical features
- •Investigations
- •Management
- •Gastroduodenal disorders
- •Gastroduodenitis and peptic ulcer disease
- •Clinical features
- •Investigations
- •Management
- •Upper gastrointestinal tract haemorrhage
- •Management
- •Gastric cancer
- •Clinical features
- •Management
- •Gastrointestinal stromal tumour
- •Small bowel disorders
- •Malabsorption
- •Coeliac disease
- •Bacterial overgrowth
- •Tropical sprue
- •Whipple disease
- •Neuroendocrine tumours of the bowel
- •Carcinoid tumours
- •Gastrinoma
- •Insulinomas
- •VIPomas
- •Glucagonomas
- •Lower gastrointestinal tract
- •Colorectal disorders
- •Colorectal neoplasia
- •Benign disease
- •Colorectal cancer
- •Screening
- •Diverticular disease
- •Clinical features
- •Investigations
- •Management
- •Clostridium difficile and pseudomembranous colitis
- •Lower gastrointestinal tract bleeding
- •Ischaemic colitis
- •Microscopic colitis
- •Irritable bowel syndrome
- •Clinical features
- •Investigations
- •Management
- •Nonulcer dyspepsia
- •Inflammatory bowel disease
- •General overview
- •Ulcerative colitis
- •Crohn disease
- •Hepatobiliary system
- •Gallbladder disorders
- •Gallstones and biliary colic
- •Clinical features
- •Investigations
- •Management
- •Acute cholecystitis
- •Clinical features
- •Investigations
- •Management
- •Recurrent cholecystitis
- •Biliary tract cancer
- •Cholangiocarcinoma
- •Gallbladder cancer
- •Cancer of the ampulla of Vater
- •Pancreatic disorders
- •Acute pancreatitis
- •Clinical features
- •Investigations
- •Management
- •Chronic pancreatitis
- •Investigations
- •Management
- •Pancreatic cancer
- •Clinical features
- •Investigations
- •Management
- •Liver disorders
- •Chronic liver disease
- •Established chronic liver disease
- •Hepatitis
- •Acute hepatitis
- •Acute viral hepatitis
- •Hepatitis A
- •Epidemiology
- •Hepatitis B
- •Hepatitis C
- •Investigations
- •Management
- •Autoimmune hepatitis
- •Alcoholic liver disease
- •Pathology
- •Clinical features
- •Investigations
- •Prognosis
- •Nonalcoholic steatohepatitis
- •Haemochromatosis
- •Investigations
- •Management
- •Primary biliary cholangitis
- •Primary sclerosing cholangitis
- •Wilson disease (hepatocellular degeneration)
- •Clinical features
- •Investigations
- •Management
- •Hepatic tumours
- •Benign tumours
- •Malignant tumours
- •Miscellaneous conditions
- •α1-Antitrypsin deficiency
- •Liver abscess
- •Budd–Chiari syndrome
- •Further reading
- •Haematuria and proteinuria
- •Proteinuria
- •Benign proteinuria
- •Pathological proteinuria
- •Overflow proteinuria
- •Clinical Features
- •Investigations
- •Urine
- •Blood tests
- •Imaging
- •Histological diagnosis
- •Acute kidney injury
- •Aetiology
- •Clinical features
- •Investigations
- •Urine
- •Blood tests
- •Other tests
- •Management
- •Hyperkalaemia
- •Acidosis
- •Pulmonary oedema
- •Renal replacement therapies
- •Supportive management
- •Summary
- •Chronic kidney disease
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Prevention of decline in renal function
- •Prevention of complications
- •Cardiovascular
- •Renal osteodystrophy
- •Acidosis
- •Anaemia
- •Hyperkalaemia
- •End-stage renal failure
- •Glomerular disease
- •Clinical features
- •Nephritic syndrome
- •Nephrotic syndrome
- •History
- •Investigations
- •Urine
- •Blood tests
- •Imaging
- •Renal biopsy
- •Management
- •Important primary and secondary glomerular diseases
- •Rapidly progressive glomerulonephritis
- •Antiglomerular basement membrane disease
- •IgA nephropathy
- •Lupus nephritis
- •Minimal change nephropathy
- •Focal segmental glomerulosclerosis
- •Membranous glomerulonephritis
- •Membranoproliferative glomerulonephritis
- •Poststreptococcal glomerulonephritis
- •Urinary tract infections
- •Lower urinary tract infections
- •Upper urinary tract infections
- •Clinical features
- •Investigations
- •Management
- •Renal calculi
- •General overview
- •Clinical features
- •Management
- •Urinary tract malignancies
- •Renal cell carcinoma
- •Transitional cell carcinoma
- •Prostatic carcinoma
- •Testicular cancer
- •Miscellaneous conditions
- •Adult polycystic kidney disease
- •Hepatorenal syndrome
- •Thrombotic microangiopathies
- •Sexually transmitted diseases
- •Chlamydia
- •Gonorrhoea
- •Syphilis
- •Further reading
- •Sodium and water balance
- •Hyponatraemia
- •Investigations
- •Hypernatraemia
- •Focal onset seizures
- •Normal awareness
- •Impaired awareness
- •Focal evolving to bilateral convulsive seizures
- •Generalized onset seizures
- •Tonic–clonic (grand mal) seizures
- •Absence attacks (petit mal)
- •Myoclonic seizure
- •Atonic or akinetic epilepsy
- •Aetiology
- •Hypokalaemia
- •Investigations
- •Management
- •Hyperkalaemia
- •Investigations
- •Management
- •Calcium balance
- •Hypocalcaemia
- •Hypercalcaemia
- •Investigations
- •32 Nervous system
- •Cerebrovascular disease
- •Stroke and TIA
- •Intracerebral haemorrhage
- •Subarachnoid haemorrhage
- •Clinical features
- •Investigations
- •Management
- •Subdural haematoma
- •Extradural haematoma
- •Headache
- •Migraine
- •General overview
- •Clinical features
- •Management
- •Cluster headache
- •Tension-type headache
- •Idiopathic intracranial hypertension
- •Trigeminal neuralgia
- •Persistent idiopathic facial pain (atypical facial pain)
- •Dementia
- •Epilepsy
- •General overview
- •Classification
- •Investigations
- •Bedside
- •Imaging
- •Electroencephalogram
- •Management
- •Drug treatment
- •First-line drugs
- •Second-line drugs
- •Withdrawing drugs
- •Other treatment
- •Status epilepticus
- •Pregnancy and epilepsy
- •Driving and work and epilepsy
- •Sudden unexpected death in epilepsy
- •Intracranial tumours
- •General overview
- •Clinical features
- •Raised intracranial pressure
- •Investigations
- •Management
- •Movement disorders
- •Parkinsonism
- •Clinical features
- •Tremor
- •Rigidity
- •Bradykinesia
- •Other features
- •Management
- •Drug therapy
- •Other therapy
- •Tremor
- •Essential tremor
- •Cerebellar tremor
- •Huntington Disease
- •Sydenham chorea
- •Other movement disorders
- •Multiple sclerosis
- •General overview
- •Pathogenesis
- •Clinical features
- •Optic neuritis
- •Diplopia
- •Sensory symptoms
- •Motor weakness
- •Cerebellar signs
- •Other manifestations
- •Investigations
- •Management
- •Central nervous system infection
- •Meningitis
- •General overview
- •Causative organisms
- •Clinical features
- •Meningism
- •Sepsis
- •Raised intracranial pressure
- •Investigations
- •Management
- •Encephalitis
- •Central nervous system abscess
- •Spinal cord infection
- •Spinal cord disorders
- •Spinal cord compression
- •Subacute combined degeneration of the cord
- •Syringomyelia and syringobulbia
- •Peripheral nervous system disorders
- •Peripheral neuropathy
- •Guillain–Barré syndrome
- •Clinical features
- •Investigations
- •Management
- •Entrapment/compression neuropathies
- •Neuromuscular disorders
- •Muscle disorders
- •Myotonic dystrophy (myotonia dystrophica)
- •Muscular dystrophy
- •Duchenne and Becker muscular dystrophy (pseudohypertrophic)
- •Facioscapulohumeral dystrophy (Landouzy–Dejerine syndrome)
- •Limb girdle dystrophy
- •Neuromuscular junction disorders
- •Myasthenia gravis
- •Clinical features
- •Investigations
- •Management
- •Lambert–Eaton myasthenic syndrome
- •Miscellaneous disorders
- •Motor neurone disease
- •Management
- •Horner syndrome
- •Bulbar and pseudobulbar palsy
- •Bell palsy
- •Further reading
- •Diabetes mellitus
- •Aetiology and Pathophysiology
- •Clinical features
- •Macrovascular disease
- •Microvascular disease
- •Diabetic retinopathy
- •Diabetic nephropathy
- •Diabetic neuropathy
- •Diabetic feet
- •Skin
- •Infections
- •Management
- •Diet and lifestyle
- •Oral hypoglycaemic agents
- •Biguanides
- •Sulphonylureas
- •Meglitinides; rapid-acting insulin secretagogues
- •Thiazolidinediones
- •Dipeptidyl peptidase 4 inhibitors
- •Glucagon-like peptide 1 agonists
- •Acarbose
- •Insulin
- •Diabetes and surgery
- •Diabetic emergencies
- •Hypoglycaemia
- •Diabetic ketoacidosis
- •Hyperosmolar hyperglycaemic state
- •Obesity and metabolic syndrome
- •Lipid disorders
- •Aetiology and pathophysiology
- •Primary hyperlipidaemia
- •Secondary hyperlipidaemia
- •Investigations
- •Management
- •Primary prevention
- •Secondary prevention
- •Drugs
- •Thyroid disease
- •Hypothyroidism
- •Management
- •Hyperthyroidism
- •Management
- •Antithyroid drugs
- •Radioiodine
- •Subtotal thyroidectomy
- •Thyroid emergencies
- •Thyrotoxic crisis (‘thyroid storm’)
- •Myxoedema coma
- •Parathyroid disease
- •Hypoparathyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Hyperparathyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Pituitary disorders
- •Hypopituitarism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Pituitary tumours
- •Clinical features
- •Investigations
- •Management
- •Acromegaly
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Surgery
- •Radiotherapy
- •Medical therapies
- •Prognosis
- •Prolactin disorders
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Diabetes insipidus
- •Cranial diabetes insipidus
- •Nephrogenic diabetes insipidus
- •Management
- •Adrenal disorders
- •Cushing syndrome
- •Clinical features
- •Investigations
- •Management
- •Cushing disease
- •Adrenocortical tumours
- •Ectopic adrenocorticotrophic hormone syndrome
- •Addison disease
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Conn syndrome (primary hyperaldosteronism)
- •Clinical features
- •Investigations
- •Management
- •Phaeochromocytoma
- •Clinical features
- •Investigations
- •Management
- •Hypothalamus–pituitary–adrenal axis
- •Dynamic tests for cortisol excess
- •Tests for cortisol deficiency
- •Pituitary function tests
- •Miscellaneous endocrine conditions
- •Multiple endocrine neoplasia
- •Autoimmune polyendocrine syndrome
- •Congenital adrenal hyperplasia
- •Metabolic bone disease
- •Osteoporosis
- •Aetiology
- •Primary osteoporosis
- •Secondary osteoporosis
- •Clinical features
- •Investigations
- •Management
- •General principles
- •Drugs
- •Paget disease
- •Clinical features
- •Investigations
- •Management
- •Bisphosphonates
- •Calcitonin
- •Surgery
- •Osteomalacia
- •Aetiology
- •Clinical features
- •Investigations
- •Biochemistry
- •Imaging
- •Management
- •Renal osteodystrophy
- •Management
- •Further reading
- •34 Musculoskeletal system
- •Osteoarthritis
- •Pathology
- •Clinical features
- •Management
- •Rheumatoid arthritis
- •Pathology
- •Clinical features
- •Management
- •Spondyloarthropathies
- •Ankylosing spondylitis
- •Pathology
- •Clinical features
- •Management
- •Reactive arthritis
- •Pathology
- •Clinical features
- •Management
- •Psoriatic arthritis
- •Enteropathic arthropathies
- •Crystal arthropathy
- •Gout
- •Pathology
- •Clinical features
- •Management
- •Pseudogout
- •Connective tissue disorders
- •Systemic lupus erythematosus
- •Pathology
- •Clinical features
- •Treatment
- •Systemic sclerosis
- •Pathology
- •Clinical features
- •Management
- •Polymyositis and dermatomyositis
- •Pathology
- •Clinical features
- •Management
- •Sjögren syndrome
- •Vasculitis
- •General overview
- •Eosinophilic granulomatosis with polyangiitis
- •Granulomatosis with polyangiitis
- •Henoch–Schönlein purpura
- •Kawasaki disease
- •Microscopic polyangiitis
- •Polyarteritis nodosa
- •Behçet disease
- •Polymyalgia rheumatica and giant cell arteritis
- •Polymyalgia rheumatica
- •Giant cell arteritis
- •Antiphospholipid syndrome
- •35 Skin disease
- •Skin manifestations of systemic disease
- •Diabetes mellitus
- •Inflammatory bowel disease
- •Coeliac disease
- •Hyperthyroidism
- •Malignant disease
- •Sarcoidosis
- •Rheumatic fever
- •Neurofibromatosis
- •Lyme disease (borreliosis)
- •Hyperlipidaemia
- •Skin disease
- •Psoriasis
- •Clinical features
- •Management
- •Eczema/dermatitis
- •Clinical features
- •Management
- •Acne vulgaris
- •Actinic keratosis
- •Seborrhoeic keratosis
- •Herpes simplex
- •Herpes (varicella) zoster
- •Lichen planus
- •Erythema multiforme
- •Stevens–Johnson syndrome and toxic epidermal necrolysis
- •Pemphigus vulgaris and bullous pemphigoid
- •Erythema nodosum
- •Vitiligo
- •Pyoderma gangrenosum
- •Neoplastic disease
- •Basal cell carcinoma
- •Squamous cell carcinoma
- •Malignant melanoma
- •Infections
- •Impetigo
- •Cellulitis
- •Necrotizing fasciitis
- •36 Haematological disorders
- •Anaemia
- •Diagnosis
- •Management
- •Iron replacement
- •Vitamin B12 and folate replacement
- •Blood transfusion
- •Splenectomy
- •Erythropoietin
- •Causes of anaemia
- •Anaemia of chronic disease
- •Clinical features
- •Management
- •Haemolytic anaemia
- •Clinical features
- •Management
- •Sickle cell anaemia
- •Clinical features
- •Management
- •Thalassaemia
- •Clinical features
- •Management
- •Aplastic anaemia
- •Clinical features
- •Management
- •Leukaemia
- •Acute lymphoblastic leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Acute myeloid leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Chronic lymphocytic leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Chronic myeloid leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Multiple myeloma
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Lymphoma
- •Hodgkin disease
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Non-Hodgkin lymphoma
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Myelodysplastic syndromes
- •Classification
- •Clinical features
- •Management
- •Myeloproliferative disease
- •Polycythaemia vera
- •Essential thrombocythaemia
- •Primary myelofibrosis
- •Bleeding disorders
- •Haemophilia A
- •Haemophilia B (Christmas disease)
- •Von Willebrand disease
- •Immune thrombocytopenia
- •Disseminated intravascular coagulation
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Thrombotic disorders and thromboembolism
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Thrombotic thrombocytopenic purpura
- •Haemolytic uraemic syndrome
- •37 Infectious diseases
- •General overview
- •HIV and AIDS
- •Epidemiology and aetiology
- •Pathology
- •Clinical features
- •Primary HIV infection
- •Clinical stage 1
- •Clinical stage 2
- •Clinical stages 3 and 4
- •Treatment and prognosis
- •Prevention
- •Malaria
- •Epidemiology and aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Prevention
- •Diarrhoeal disease
- •Drug-resistant bacteria
- •Other resistant bacteria
- •38 Drug overdose and abuse
- •General overview
- •Common presentation, investigations and management
- •History
- •Examination
- •How ill is the patient?
- •Is there any evidence to suggest an underlying cause?
- •Have any complications occurred?
- •Investigations
- •Management
- •Supportive care
- •Preventing absorption
- •Increase elimination of drug
- •Specific antidotes
- •Psychiatric and social assessment
- •Paracetamol overdose
- •Illegal drugs
- •Alcohol misuse and withdrawal
- •Alcohol withdrawal
- •Wernicke encephalopathy/Korsakoff psychosis
- •Long-term treatment
- •Further reading
- •Self-Assessment
- •SBA answers
- •EMQ answers
- •Index

Index
Gottron papules, 343
gout, 147t
clinical features, 340
management, 340
pathology, 340
gouty tophi, 14
granulomatosis with polyangiitis, 344
Graves disease, 109
Grey Turner sign, 67
Guillain-Barre´ syndrome
clinical features, 299
investigations, 299
management, 299
guttate psoriasis, 348, 348f
H
HAART therapy, 376–378
haemarthrosis, 147, 160
haematemesis, 66
differential diagnosis, 75t
examination, 76, 76f
history, 75–76
investigations, 76–79, 77f
Rockall score, 78t
haematological disorders
anaemia, 76, 357–362
bleeding disorders, 370–371
clinical features, 8
disseminated intravascular coagulation,
371–372
haemolytic uraemic syndrome, 374
leukaemia, 362–365
lymphoma, 366–369
multiple myeloma, 365–366
myelodysplastic syndromes, 369
myeloproliferative disease, 369–370
thromboembolic disorders, 372–374,
373t
thrombotic thrombocytopenic purpura,
374
haematuria, 96–99
causes, 97t
examination, 97–99
history, 97–99
investigation, 98f, 254, 255f
haemochromatosis
classification, 249
investigations, 249–250
management, 250
prevalence, 249
haemoglobin synthesis, 360, 360t
haemolysis screen, 92
haemolytic anaemia, 359
autoimmune, 359
clinical features, 359
immune, 359
management, 359
nonimmune, 359
haemolytic uraemic syndrome (HUS),
271, 374
haemophilia A, 370–371
haemophilia B (Christmas disease),
371
haemoptysis, 47
differential diagnosis, 53b
examination, 54, 55f
history, 53–54
investigations, 54–56
haemorrhage
splinter, 14
subarachnoid, 101, 283
haemostasis, 160
hands, 13–14, 20
clubbing of fingers (see clubbing)
HAV. See hepatitis A virus
HBV. See hepatitis B virus
HCV. See hepatitis C virus
HDV. See hepatitis D virus
headache, 6, 284–285
atypical facial pain, 285
chronic headache, 102–103
cluster headache, 285
differential diagnosis, 101, 101t
examination, 103–104, 103f
history, 101–103
idiopathic intracranial hypertension,
285
migraine, 102
migraine, 284–285
progressive, 102, 102b
recurrent episodic, 102
tension-type headache, 285
trigeminal neuralgia, 285
head impulse test, 143
Heaf test, 218
hearing, altered, 6
heart. See cardiac; cardiovascular
heart block, 175, 178
heartburn
causes, 71b
examination, 71
history, 71
investigations, 72–73, 72f
heart failure, 180–183
acute, 182
aetiology, 180–181
chronic, 182–183
clinical features, 181
investigations, 181
left-sided, 181
management of, 182–183
right-sided, 181
heart murmurs, 191–192, 194
heart transplantation, 183
heat rash, 154
heaving, 17
Heberden nodes, 14
Helicobacter pylori, 73
hemiplegia, 138t
Henoch-Schönlein purpura, 344–345
heparin, 162, 386t
overdose, 385, 386t
hepatic encephalopathy, 245
hepatitis
acute, 246–248
autoimmune, 248
viral, 246–248
hepatitis A virus, 246
hepatitis B virus, 246
hepatitis C virus, 246–247
hepatitis D virus, 247
hepatitis E, 247
hepatobiliary system
biliary tract cancer
cancer of ampulla of vater, 243
cholangiocarcinoma, 242
gallbladder cancer, 242
gallbladder disorders
acute cholecystitis, 242
gallstones and biliary colic, 241–242
liver disorders
abscess, 251
alcoholic liver disease, 248–249
α1-antitrypsin deficiency, 251
Budd–Chiari syndrome, 251–252
chronic liver disease, 244–245
haemochromatosis, 249–250
hepatic tumours, 251
hepatitis, 246–248
nonalcoholic steatohepatitis, 249
primary biliary cholangitis, 250
primary sclerosing cholangitis, 250
Wilson disease, 250–251
pancreatic disorders
acute pancreatitis, 243–244
chronic pancreatitis, 244
pancreatic cancer, 244
hepatocellular screen, 92
hepatomegaly, 22t
hepatorenal syndrome (HRS), 271
chronic liver disease, 245
hereditary haemorrhagic telangiectasia, 163
hereditary nonpolyposis colon cancer, 235
hernia, 67
heroin, 385, 387t
herpes simplex, 154, 352
and HIV/AIDS, 378, 379t
herpes zoster, 154, 155f, 352
and HIV/AIDS, 378, 379t
hiatus hernia, 229–230
high-density lipoprotein (LDL), 168
high-dose dexamethasone suppression
test, 328
history taking. See also specific conditions
bedside manner, 1
family history, 2
medical history, 2
medications and allergies, 2
presenting complaint, 1–2
social history, 3, 3f
systems review, 3–8
HIV/AIDS, 375–379
clinical features, 376, 376t
epidemiology and aetiology, 375, 375t
opportunistic infections, 378, 379t
448

Index
HIV/AIDS (Continued)
pathology, 375, 375t
prevention, 379
primary HIV infection, 376, 377–378t
treatment and prognosis, 376–379, 378f,
379t
hoarseness, 5
Hodgkin disease
aetiology, 367
clinical features, 367, 367f
pathology, 367, 367t
treatment and prognosis, 367–368
Holter monitoring, 175
Horner syndrome, 24, 302
hospital acquired (nosocomial)
pneumonia, 210, 212t
Huntington disease, 293–294
hydralazine, for heart failure, 182
hydrocephalus, 102
hypercalcaemia, 281
causes of, 281, 281t
investigations, 281
treatment of, 281
hyperextensibility, 159
hyperhaemolytic anaemia, 360
hyperkalaemia, 258–259, 262, 278–279
causes of, 278, 278t
EKG changes in, 279, 279f
investigations, 279
management, 279
hyperkeratotic lesions, 156
hyperlipidaemia
and ischaemic heart disease, 168
primary, 314
skin manifestations, 347–348 (see lipid
disorders)
hypernatraemia, 277–278
causes of, 277, 277t
hyperosmolar hyperglycaemic state, 313
hyperparathyroidism
aetiology, 318
clinical features, 318
investigations, 318–319
management, 319
hyperprolactinaemia, 322, 322t
hypertension, 183–187
clinical features, 184
control in pregnancy, 187
idiopathic intracranial, 167
investigations, 184–185
and ischaemic heart disease, 168
malignant, 187
management, 185–187
hyperthyroidism, 109–110, 316. See also
thyrotoxicosis
aetiology, 109
clinical features, 109
investigations, 110
primary, 109
skin manifestations, 347
hypertrophic obstructive cardiomyopathy,
193–194
hypoalbuminaemia, 14t
hypocalcaemia, 280–281
causes of, 280, 280t
hypoglossal nerve, 28
hypoglycaemia, 311–312
hypokalaemia, 278
causes of, 278, 278t
investigations, 278
management, 278
hyponatraemia, 275–277
diagnostic algorithm, 275, 276f
investigations, 276–277
hypoparathyroidism
aetiology, 317, 318t
clinical features, 317
investigations, 318
management, 318
hypopituitarism
aetiology, 319
clinical features, 319
investigations, 319–320
management, 320
hypothyroidism, 108–109, 316
aetiology, 108
clinical features, 108
investigations, 109
palpitations, 58
hypoventilation syndromes, 224
hypovolaemia, 76
I
iatrogenic hypothyroidism, 108
iatrogenic pneumothorax, 219
IBD. See inflammatory bowel disease
(IBD)
IBS. See irritable bowel syndrome (IBS)
icterus. See jaundice
idiopathic atrophic thyroiditis, 108
idiopathic pulmonary fibrosis (IPF), 223
IgA nephropathy, 265–266
ileus, 22b
illegal drugs, 385, 387t, 388
imaging. See also chest X-ray
abdominal pain, 68
back pain, 147–148
bowel habits, 82–83
cough/haemoptysis, 55
focal neurological deficits, 138–139
glomerular disease, 264
goitre, 108
headache/facial pain, 104
heart failure, 181
hypothyroidism, 109
joint pain, 147–148, 147t
pneumonia, 211
proteinuria, 255
stroke, 126
thyroid, 110
urinary symptoms, 96
vertigo, 144
weight loss, 87
immune thrombocytopaenia (ITP), 371
impalpable, 17
impetigo, 155, 355
implantable cardioverter defibrillator, 183
incontinence
urge, 94
urinary, 6
indigestion, 5
causes, 71b
examination, 71
history, 71
investigations, 72–73, 72f
indurated lesions, 152t
infections
cellulitis, 356, 356f
central nervous system
meningitis, 101
impetigo, 355, 355f
necrotizing fasciitis, 356
signs of, 119
infectious diseases, 263, 375. See also
specific diseases
HIV/AIDS, 375–379
infective endocarditis, 194–196
clinical features, 194–195
management, 195–196
inflammatory bowel disease (IBD), 340.
See also specific conditions
cause, 238
Crohn disease, 240–241
skin manifestations, 347
ulcerative colitis, 239–240
inflammatory markers, 61
infliximab, 240, 337, 338t, 349, 349t
insulin, 310, 311f
insulinomas, 234
intention tremor, 14
international normalized ratio
(INR), 160
interstitial lung disease (ILD)
aetiology, 222
Aspergillus, 223–224
causes, 222
clinical features, 222
idiopathic pulmonary fibrosis, 223
investigations, 222, 222t
management, 222
occupational, 223, 223t
sarcoidosis, 223
intertrigo, 154
intraaortic balloon counterpulsation, 182
intracerebral haemorrhage, 283–284
intracranial pressure, raised, 102–103b
intracranial tumours, 290
meningitis, 296
intracranial tumours
clinical features, 290
investigations, 290
management, 290
origins, 289–290, 290t
primary brain, 289–290
secondary brain, 289–290
449

Index
intraepidermal squamous cell carcinoma,
154
intrinsic liver disease, 159
iodine-deficient hypothyroidism, 108
iron-deficiency anaemia. See anaemia
iron replacement, 357
irritable bowel syndrome (IBS), 237
ischaemic colitis, 237
ischaemic heart disease (IHD), 167–168.
See also cardiovascular disease
(CVD)
itching. See pruritus
itching, skin lesions, 151
ITP. See immune thrombocytopaenia
(ITP)
ivabradine, for heart failure, 183
J
janeway lesions, 15
jaundice, 5, 13, 16, 67, 76
biochemical abnormalities in, 92t
causes, 89–90
differential diagnosis, 90t
examination, 90–91, 90f
history, 89
investigations, 91–92, 91f
joint(s)
aspiration, 147
examination, 14
joint position sense, 298
swelling, 8
joint disease. See also musculoskeletal
disorders
differential diagnosis, 148, 148f
examination, 146–147, 146t
history, 145–146
investigations, 147–148
jugular venous pressure (JVP),
15–16, 58
vs carotid pulsation, 16t
jugular venous waveform, abnormalities
of, 16f
K
Kallmann syndrome, 23
Kartagener syndrome, 224
Kawasaki disease, 345
keratoacanthoma, 354
Kernig sign, 104, 296, 296f
ketamine, 385, 387t
ketoacidosis, 312–313
kidney
loop of Henle, 93
palpable, 22t, 185f
Kimmelstiel–Wilson lesion, 307
Köbner phenomenon, 152t, 353
koilonychia, 13
Kussmaul respiration, 49
kyphoscoliosis, 48
L
lactate dehydrogenase (LDH), 172, 221
Lambert-Eaton myasthenic syndrome, 301
Landouzy-Dejerine syndrome. See
Facioscapulohumeral dystrophy
large cell (anaplastic) carcinoma, 213
lateral sclerosis, primary, 301
lead pipe rigidity, 28, 291
left ventricular assist devices, 183
legs. See lower limb
lentigines, 153
leuconychia, 13
leucopoenia, 61
leukaemia
acute lymphoblastic, 362–363, 363t
acute myeloid, 363–364, 363–364t
chronic lymphocytic, 364–365
chronic myeloid, 365
multiple myeloma, 365–366
levodopa (L-DOPA), 292
Lhermitte sign, 294
lichenification, 152t
lichen simplex chronicus, 153
Lichtheim disease, 298
lidocaine, 180
limb girdle dystrophy, 300
limbs
lower (see lower limbs)
upper (see upper limbs)
lipid disorders. See also individual drugs
aetiology and pathophysiology, 314
investigations, 314
management, 314–315
skin manifestations, 347–348
lipid-lowering drugs, 170
lipid-regulating drugs, 315
lipoatrophy, 308
lip pursing, 49
lisinopril, 182
liver abscess, 251
liver disease, 159, 162
prothrombin time, 78
liver disorders
abscess, 251
alcoholic liver disease, 248–249
α1-antitrypsin deficiency, 251
Budd–Chiari syndrome, 251–252
chronic liver disease, 244–245
haemochromatosis, 249–250
hepatic tumours, 251
hepatitis, 246–248
nonalcoholic steatohepatitis, 249
primary biliary cholangitis, 250
primary sclerosing cholangitis, 250
Wilson disease, 250–251
liver function tests, 160
focal neurological deficits, 138
PUO, 61
liver tumours, 251
localized lymphadenopathy, 130
loin pain, 6
long synacthen test, 328
loss of consciousness, 4
differential diagnosis, 111t
examination, 112–114, 113f
history, 111–112
investigations, 114–115
risk factors, 112
low-density lipoprotein (LDL), 168
lower gastrointestinal tract
bleeding, 236–237
Clostridium difficile, 236
colorectal disorders, 234–236
inflammatory bowel disease, 238–241
irritable bowel syndrome, 237
ischaemic colitis, 237
microscopic colitis, 237
nonulcer dyspepsia, 237–238
pseudomembranous colitis, 236
lower limbs
coordination, 31
oedema, 23t
power, 31
reflexes, 31
sensation, 31–32
tone, 30
visual survey, 30
lower urinary tract infections, 267
low-molecular-weight heparin (LMWH),
213
lumbar plexus, 133–135t
lumbar puncture, 104
lumps
anatomical distribution and causes, 130t
differential diagnosis, 130–131
examination, 129–130
history, 129–130
investigations, 130
lung cancer
aetiology, 214, 214t
clinical features, 214–215
five-year survival rates, 214t
investigations, 215
management, 215–216, 216t
paraneoplastic syndrome, 215, 215t
pathology, 214
TNM staging, 215, 216t
treatment strategies for, 216t
types, 213
lung disease, 194
lupus nephritis, 266
Lyme disease, 347
lymphadenopathy, 33–34, 76
abdominal pain, 67
lymph node sites, 34f
lymphocytosis, 61
lymphoma, 366–369
Hodgkin disease, 367–368, 367t
myeloma and immunoproliferative
disorder, 366–368, 367t
non-Hodgkin, 367f, 368–369, 368t
Lynch syndrome. See hereditary
nonpolyposis colon cancer
450

Index
M
macrophages, 168
macrovascular disease, 307
macule, 152t
maculopapular lesions, 156–157
magnesium sulphate, 180
magnetic resonance imaging (MRI), 108,
139, 215
Major Jones criteria, 196
malabsorption, 162, 232–234, 233t
malar flush, 16
malaria
clinical features, 380–381, 380t
diarrhoeal disease, 381–382,
381–382t
epidemiology and aetiology, 379–380,
380t
pathology, 380, 380f, 380t
prevention, 381
treatment and prognosis, 381
malaria transmission cycle, 380, 380f
malignancy, 160
malignant disease, 347
malignant melanoma, 354–355, 355f
malignant tumours, 251
Mallory-Weiss tear, 75t
massive blood loss protocol, 12
MDMA, 385, 387t
MDS. See myelodysplastic syndromes
(MDS)
medical documentation, 37t
medical history, 2
medications, 2. See also specific drugs
medullary thyroid carcinoma, 110
mefloquine, 381
meglitinides, 310
melaena, 5
differential diagnosis, 75t
examination, 76, 76f
history, 75–76
investigations, 76–79, 77f
Rockall score, 78t
melanocytic naevus (mole), 153
melanoma, 153, 354–355
melasma, 153
membranoproliferative
glomerulonephritis, 266–267
membranous glomerulonephritis, 266
Ménière disease, 142t
meningism, 104b, 296
meningitis, 101
causative organisms, 296
cerebrospinal fluid, 297, 297t
clinical features, 296
cryptococcal, 378, 379t
investigations, 297
management, 297
menstruation, 6
mephedrone, 385, 387t
meralgia paraesthetica, 300
mesalazine, 239–240
metabolic/endocrine disorders, 7
andenal disorders, 323–328
autoimmune polyendocrine syndrome,
329
bone disease, 329–334
congenital adrenal hyperplasia, 329
diabetes mellitus (see diabetes mellitus)
lipid disorders, 314–315
metabolic syndrome, 313–314
multiple endocrine neoplasia,
328–329
obesity, 313–314
pituitary disorders, 319–323
thyroid disease, 315–319
methicillin-resistant Staphylococcus aureus
(MRSA), 382
metoprolol, 170
microbiology tests, 62
micropsia, 284
microscopic colitis, 237
microscopic polyangiitis, 345
microvascular disease
diabetic nephropathy, 307–308
diabetic neuropathy, 308
diabetic retinopathy, 307
migraine, 102. See also headache
syndromes
clinical features, 284
general overview, 284
management, 284
miliaria, 154
milrinone, 182
minimal change nephropathy, 266
minoxidil, 187
mitral regurgitation, 175, 189–190
clinical features, 189
management, 190
mitral stenosis, 188–189
clinical features, 188
management, 189
mitral valve prolapse, 190
mitral valvotomy scar, 17
monoamine oxidase B inhibitors, 293
monocytosis, 61
mononeuritis, 308
motor neurone disease, 301
motor weakness, 294
mouth, 16
movement disorders
Huntington disease, 293–294
other movement disorders, 294
parkinsonism, 291–293
Sydenham chorea, 294
tremor (see tremor)
MRSA. See Methicillin-resistant
Staphylococcus aureus (MRSA)
multiple endocrine neoplasia, 328–329
multiple myeloma, 365–366
aetiology, 365–366
clinical features, 366
pathology, 366
treatment and prognosis, 366
multiple sclerosis
clinical features, 294–295
diagnosis, 295, 295b
investigations, 295
management, 295–296
pathogenesis, 294
muscle disorders
muscular dystrophy, 300
myasthenia gravis, 300–301
myotonic dystrophy, 300
musculoskeletal disease, 138t
musculoskeletal disorders, 7–8. See also
specific conditions
musculoskeletal examination
assessment of disability, 33
feel, 33
look, 33
move, 33
visual survey, 33
musculoskeletal system
antiphospholipid syndrome, 346
connective tissue disorders, 341–344
crystal arthropathy, 340–341
giant cell arteritis, 346
osteoarthritis, 335–336
polymyalgia rheumatica, 345–346
rheumatoid arthritis, 336–338
spondyloarthropathies, 336–338
vasculitis, 344–345
Mycobacterium
M. avium complex, 378, 379t
M. tuberculosis, 216–218
myelodysplastic syndromes (MDS), 162,
369
classification, 369, 369t
clinical features, 369
management, 369
myelofibrosis, 370
primary, 370
myeloproliferative disease, 162, 369–370
essential thrombocythaemia, 370
polycythaemia vera, 369–370
primary myelofibrosis, 370
myocardial infarction, 169t, 171b
myocardial muscle creatine kinase (CK-
MB), 172
myoclonic seizure, 287–288
myotonia, 14
myotonic dystrophy/myotonia
dystrophica, 300
myotonic pupil, 24
myxoedema coma, 317
N
naevus, 153
nails, 13–14
NASH. See nonalcoholic steatohepatitis
(NASH)
natalizumab, 295–296
National Institute for Health and Care
Excellence (NICE), 170b, 182
451

Index
nausea, 5
nebivolol, 182
neck clinical examinations, 34
necrotizing fasciitis, 356
neoplastic disease, 353–355
basal cell carcinoma, 353–354, 354f, 354t
malignant melanoma, 354–355, 355f
squamous cell carcinoma, 354, 354f
nephritic syndrome, 263
nephrogenic diabetes insipidus, 323, 323t
nephrotic syndrome, 253t, 263
nervous system
clinical signs, 23
cranial nerves, 23–28
symptoms, 6
visual survey, 23–28
neurodegenerative disorder, 287
neuroendocrine tumours. See specific types
neurofibromatosis, 347
neuroimaging, 288
neuromuscular examination, 14
neuromuscular junction disorders
clinical features, 300–301
investigations, 301
management, 301
neuropathic ulcers, 157
neutrophilia, 61
NHL. See non-Hodgkin lymphoma (NHL)
nicorandil, 170
nifedipine, 170
nitrates, 170
nocturia, 6, 93
nodular lesions, 156
nodule, 152t
‘no known drug allergies’ (NKDA), 2
nonalcoholic steatohepatitis, 249
non-Hodgkin lymphoma (NHL)
aetiology, 368
clinical features, 368
multifactorial cause, 368
pathology, 368, 368t
treatment and prognosis, 368–369
non-nucleoside reverse transcriptase
inhibitors, 378, 378f
non ST elevation myocardial infarction
(NSTEMI), 172–175
nonsteroidal antiinflammatories
(NSAIDs), 337–338
nonulcer dyspepsia, 237–238
non-vitamin K antagonist oral
anticoagulants, 213
Noonan syndrome, 191, 198
NSAIDs. See nonsteroidal
antiinflammatories (NSAIDs)
NSTEMI. See non ST elevation myocardial
infarction (NSTEMI)
N-terminal pro-B-type natriuretic peptide,
181
nuclear imaging, 169
nucleoside reverse transcriptase inhibitors,
378, 378f
nystagmus, 143
452
O
OA. See osteoarthritis (OA)
obesity, 313–314
and hypertension, 183–187
hypoventilation syndrome, 224
and ischaemic heart disease, 168
obstructive sleep apnoea (OSA)
syndrome, 224
occipital lobe, 290
occupational lung disease, 223, 223t
oculomotor nerve, 25–26
oedema, 4. See also swelling
lower limbs, 23, 23t
oesophageal cancer, 230
oesophageal disorders
achalasia, 230
Barrett oesophagus, 230
eosinophilic oesophagitis, 230
gastro-oesophageal reflux
disease, 229
hiatus hernia, 229–230
oesophageal cancer, 230
oesophageal motility disorders, 230
oesophageal motility disorders, 230
oesophageal varices, 75t
oesophagitis, 75t
olfactory nerve, 23
oliguria, 93
omeprazole, 229
Ondine curse, 224
onycholysis, 14
ophthalmoscopy, 24
opiate overdose, 385, 386t
opiates, 386t
opportunistic infections, 378, 379t
opportunistic pneumonia, 210
optic atrophy, 24t
optic nerve, 23–25
optic neuritis, 294
oral anticoagulants
treatment, 213
types of, 213
oral hypoglycaemic agents
acarbose, 310
biguanides, 309
dipeptidyl peptidase 4 inhibitors, 310
glucagon-like peptide
1agonists, 310
meglitinides, 310
sulphonylureas, 309–310
thiazolidinediones, 310
oral mucolitics, 209
orthopnoea, 4
orthostatic proteinuria, 253
Osler nodes, 15
Osler-Weber-Rendu disease, 76
osmotic diuresis, 94t
osteoarthritis (OA), 147t
clinical features, 335
management, 335–336
pathology, 335, 335f
osteomalacia
aetiology, 332
biochemistry, 332
clinical features, 332
imaging, 332–333
management, 333
osteopenia, 330–331
osteoporosis
aetiology, 330
clinical features, 330
drugs, 330–331
investigations, 330
primary, 330
principles, 330
overflow proteinuria, 254
overnight dexamethasone suppression
test, 328
overriding aorta, 198
oxygen therapy, 204, 204–205t, 208
P
PA. See psoriatic arthritis (PA)
Paco2, 201
Paget disease, 331–332
clinical features, 331–332
features, 331, 331f
investigations, 332
management, 332
pain
abdominal, 5
bone, 8t
chest, 4
epigastric, 122
loin, 6
musc ula r, 7
sensory testing, 30, 31t
thigh, 4
pallor, 12
palmar erythema, 14t
palpation, 17
dyspnoea, 50
palpitations, 4, 178
causes, 57–58
consequences of, 58b
differential diagnosis, 57, 57f
examination, 58, 59f
history, 57
investigations, 58–59
PAN. See polyarteritis nodosa (PAN)
Pancoast symptoms, 18
pancreatic cancer, 244
pancreatic disorders
acute pancreatitis, 243–244
chronic pancreatitis, 244
pancreatic cancer, 244
papillary thyroid carcinoma, 110
papilloedema, 24t
papular lesions, 156
papule, 152t
paracetamol overdose, 385, 386t, 388
paraneoplastic syndrome, 215, 215t

Index
parathyroid disease
hyperparathyroidism, 318–319
hypoparathyroidism, 317–318
parietal lobe, 290
parkinsonism, 138t
clinical features, 291–292
differential diagnosis, 291, 291t
management, 292–293
typical posture in, 291, 292f
Parkinson disease, 291
paroxysmal nocturnal dyspnoea, 4
paroxysmal nocturnal haemoglobinuria,
372, 373t
paroxysmal supraventricular tachycardia,
177
past medical history, 2
patch, 152t
patent ductus arteriosus (PDA), 197
patients, visual assessment, 12–13
PBC. See primary biliary cholangitis (PBC)
peak expiratory flow rate (PEFR), 203
pemphigus, 156
pemphigus vulgaris, 353
penile discharge, 6
peptic ulcer disease, 75t
percussion, 50
percutaneous coronary intervention (PCI),
46, 170
pericardial effusion, 192–193
pericarditis, 192–193
clinical features, 192–193
constrictive, 193
management, 193
myocardial infarction and, 175
perilymphatic fistula, 142, 142t
perindopril, 182
peripheral nervous system disorder
entrapment/compression neuropathies,
299–300
Guillain-Barré syndrome, 299
peripheral neuropathy, 299–300
peripheral neuropathy, 299
peritonism, 66, 67t
pernicious anaemia, 357
persistent idiopathic facial pain. See
atypical facial pain
petechiae, 152t
petechial lesions, 157
Peutz–Jeghers syndrome, 76, 235
phaeochromocytoma
clinical features, 327
cortisol deficiency, 328
cortisol excess tests, 328
hypothalamus-pituitary- andrenal axis,
324f, 327–328
investigations, 327
management, 327
pituitary function tests, 328
pharyngoscopy, 55
Philadelphia chromosome, 365
photodermatoses, 156
Pickwickian syndrome, 224
pigmentation, 13
pigmented lesions, 153
pioglitazone, 310
pituitary apoplexy, 319
pituitary disorders
acromegaly, 320–322
diabetes insipidus, 94t, 323
hypopituitarism, 319–320
prolactin disorders, 322–323
tumours, 320
pituitary function tests, 328
pituitary tumours
clinical features, 320
investigations, 320
management, 320
pityriasis versicolor, 154, 154f
plaque, 152t
plaque psoriasis, 348, 348f
plasma viscosity, 366
Plasmodium spp., 380–381, 380–381t
platelet
abnormalities, 159, 162
count, 162
dysfunction, 162
function tests, 161
platelet function analyser (PFA), 161
pleural effusion, 221–222
aetiology, 221
clinical features, 221
investigations, 221–222
management, 222
pleural fluid aspiration, 221–222
pleural tap, 211
pleuritic chest pain, 43
PMR. See polymyalgia rheumatica (PMR)
Pneumocystis jirovecii, 378, 379t
pneumonia, 209–211
aetiology, 210
aspiration, 210
atypical, 210
clinical features, 210
community-acquired (CAP), 210
hospital acquired (nosocomial), 210
investigations, 210–211
management, 211, 212t
opportunistic, 210
severity, 211
typical, 210
pneumothorax
catamenial, 219
clinical features, 219
iatrogenic, 219
management, 219–221, 220f
primary spontaneous, 219
secondary spontaneous, 219
spontaneous, 219
tension, 219
traumatic, 219
polyarteritis nodosa, 345
polyarthritis, 196
polycythaemia vera, 369–370
polydipsia, 93, 95
investigations, 96, 96b
psychogenic, 94t
polymyalgia rheumatica
(PMR), 345–346
polymyositis
clinical features, 343
management, 343
pathology, 343
polyuria, 93, 95
differential diagnosis, 94t
investigations, 96
pompholyx, 154
porphyria cutanea tarda, 156
positive tuberculin testing, 218
postherpetic neuralgia, 102
poststreptococcal glomerulonephritis, 267
potassium channel activators, 170
praecordium, 17
prasugrel, 173
pregnancy
and epilepsy, 289
hypertension control, 187
presenting complaint, 1–2
pretibial myxoedema, 109
primary biliary cholangitis, 250
primary hyperaldosteronism. See Conn
syndrome
primary hyperlipidaemia, 314
primary hyperthyroidism, 109
primary lateral sclerosis, 301
primary myelofibrosis, 370
primary osteoporosis, 330
primary sclerosing cholangitis, 250
primary spontaneous pneumothorax, 219
primary thyroid lymphoma, 110
procyclidine, 293
progressive bulbar palsy, 301
progressive muscular atrophy, 301
prolactin disorders
aetiology, 322, 322t
clinical features, 322–323
investigations, 323
management, 323
propranolol, 317
prostate-specific antigen (PSA), 270
prostatic carcinoma, 270
protein-to-creatinine ratio (PCR), 253–254
proteinuria, 99
benign, 253
blood tests, 254–255
clinical features, 254
definition, 253
differential diagnosis, 254
histological diagnosis, 255–256
investigations, 254–256, 255f
levels, 253, 253t
overflow, 254
pathological, 253–254, 253t
protein-to-creatinine ratio/albumin-to-
creatinine ratio, 254
urine, 254
453

Index
prothrombin time (PT), 160
liver disease, 78
proximal myopathy, 138t
pruritus, 3, 4t, 8
pseudobulbar palsy, 302
pseudogout, 341
pseudomembranous colitis, 236
Pseudomonas spp., 382
P. aeruginosa, 210
pseudoxanthoma elasticum, 159
psoriasis, 153, 348–349
clinical features, 348
management, 349, 349t
psoriatic arthritis (PA), 339–340
psychiatric abnormalities, 295
pulmonary embolism, 46b, 212–213
clinical features, 212, 212t
investigations, 212–213
management, 213
risk factors, 212
pulmonary fibrosis, 18, 19t
clinical findings, 48, 48t
pulmonary oedema, 259
pulmonary rehabilitation, 208
pulmonary stenosis, 198
pulmonary tuberculosis, 217
pulmonary valve lesions, 191–192
pulse, 18
abdominal pain, 66, 67f
pulse pressure, 15
pulsus paradoxus, 15
PUO. See pyrexia of unknown origin
(PUO)
purpura, 152t
purpuric lesions, 157
pustular lesions, 155
pustule, 152t, 155
pyoderma gangrenosum, 347
pyrazinamide, 218
pyrexia, 67
pyrexia of unknown origin (PUO)
causes, 63t
definition, 61
differential diagnosis, 62
examination, 61, 62f
history, 61
investigations, 61–62
pyuria, 94
Q
‘question mark’ posture, 338
Quincke sign, 14–15, 191
R
RA. See rheumatoid arthritis (RA)
rachitic rosary, 332
radial nerve palsy, 300
radial pulse, 15
radical prostatectomy, 270
radioiodine, 317
radionuclide imaging, 108
radiotherapy, 368
acromegaly, 322
colorectal cancer, 235–236
intracerebral tumours, 290
lung cancer, 215–216
oesophageal cancer, 230
testicular cancer, 270
raloxifene, 330
ramipril, 182
ranitidine, 229
rapidly progressive glomerulonephritis, 265
rasagiline, 293
rashes, 8, 151. See also skin lesions
intertrigo, 154
miliaria, 154
red and scaly, 153f
Raynaud phenomenon, 342
reactive arthritis
clinical features, 339
management, 339
pathology, 339
rectal bleeding, 5, 5b, 66
recurrent cholecystitis, 242
reflexes, 30, 30f
Refsum disease, 24
relative afferent pupillary defect (RAPD),
24
renal biopsy
acute kidney injury, 258
glomerular disease, 264
renal calculi
clinical features, 268–269
factors, 268
management, 269
renal cell carcinoma, 269
renal Doppler scan, 258
renal osteodystrophy, 261, 333–334
renal replacement therapies, 259
renal ultrasound, 264
reperfusion, 175
resistant gram-negative bacteria,
382
respiratory disease, 4–5
respiratory failure
type I, 201–202
type II, 202–203
respiratory system
acute respiratory distress syndrome,
224–225
Aspergillus spp., 223–224
asthma, 203
auscultation, 20
blood pressure, 18
bronchiectasis, 209
clinical examination, 17–20
COPD, 206–209
cystic fibrosis, 225–226
expansion, 18–20
face and mouth, 18
hands, 18
hypoventilation syndromes, 224
respiratory system (Continued)
inspection, 18
interstitial lung disease, 222–224
jugular venous pressure, 18
lung cancer, 213–216
occupational lung disease, 223, 223t
percussion, 20
pleural effusion, 221–222
pneumonia, 209–211
pneumothorax, 219–221
position, 18
pulmonary embolism, 212–213
pulse, 18
sarcoidosis, 223
sleep-related disorders, 224
tactile fremitus, 20
thorax, 18–20
trachea, 18, 18t
tuberculosis, 216–218
visual survey, 17–18
vocal fremitus, 20
resting tremor, 14
restrictive/infiltrative cardiomyopathy, 194
retinopathy, 24, 25t, 307–308
revascularization, 170–171
rheumatic fever, 196
Major Jones criteria, 196
management, 196
skin manifestations, 347
rheumatoid arthritis (RA), 147t
clinical features, 336–337, 336f, 337t
anaemia, 337t
extraarticular features, 337t
finger and hand abnormalities, 336f
investigations, 336
management, 337–338, 338t
DMARDs, 337–338, 338t
NSAIDs, 337–338
steroids, 337–338
surgery, 337–338
pathology, 336
rickets, 332
rifampicin, 218
riluzole, 301
risedronate, 332
rivaroxaban, 173
Rockall score, 78, 78t
Romberg test, 143
S
salbutamol, 204, 204–205t
sarcoidosis, 222t, 223, 347
skin manifestations, 347
scabies, 155, 155f
scale, 152t
scaly lesions, 153–154
sc ar, 152t
sclerodactyly, 14
sclerosing cholangitis, primary, 250
seborrhoeic dermatitis, 153, 153f, 350f, 350t
seborrhoeic keratosis, 153, 153f, 352
454

Index
secondary hyperlipidaemia, 314
secondary hyperthyroidism, 109
secondary osteoporosis, 330
secondary spontaneous pneumothorax, 219
second-degree heart block, 178
seizures. See epilepsy; and specific
conditions
selegiline, 293
sensory symptoms, 294
sepsis, 225, 296
serology. See also specific conditions
PUO, 61
sex, and ischaemic heart disease, 167
sexually transmitted infections (STIs), 272
Chlamydia trachomatis, 272
gonorrhoea, 272
syphilis, 272–273
shingles, 154. See also herpes zoster
short synacthen test, 328
SIADH. See syndrome of inappropriate
secretion of antidiuretic hormone
(SIADH)
sickle cell anaemia, 359–360
clinical features, 359–360
management, 360
sick sinus syndrome, 178
sideroblastic anaemia, 369, 369t
sigmoidoscopy, 82
simvastatin, 315
sinus bradycardia, 58b, 175, 178
sinus tachycardia, 58b, 175
Sjögren syndrome, 343–344
skeletal deformities, 17
skin diseases, 8, 151b
bullous pemphigoid, 353
eczema/dermatitis, 349–351
erythema multiforme, 353
erythema nodosum, 353
herpes simplex, 352
psoriasis, 348–349
pyoderma gangrenosum, 353
Stevens-Johnson syndrome, 353
systemic disease-related, 347–348
toxic epidermal necrolysis, 353
vitiligo, 353
skin lesions
bullous, 156
candidiasis, 157
cellulitis, 157
erysipelas, 157
examination, 151–152
figurate erythema, 155–156
history, 151
investigations, 152–153
maculopapular, 156–157
papular and nodular, 156
petechial and purpuric, 157
photodermatoses, 156
pigmented, 153
sc aly, 153–154
staphylococcal scalded skin syndrome, 157
Stevens-Johnson syndrome, 157
skin lesions (Continued)
toxic epidermal necrolysis, 157
ulcerated, 157
vesicular, 154–155
weepy/pustular, 155
SLE. See systemic lupus erythematosus
(SLE)
sleep pattern, 3
sleep-related disorders, 224
small bowel disorders
bacterial overgrowth, 233
coeliac disease, 233
malabsorption, 232–234, 233t
neuroendocrine tumours of
bowel, 234
tropical sprue, 233
Whipple disease, 234
small cell (oat cell) carcinoma, 213
smell, altered, 6
smoking
and COPD, 206, 208
and ischaemic heart disease, 168
lung cancer, 214, 214t
social history, 3, 3f
SOCRATES mnemonic, 66
sodium homeostasis, 275
somatic neuropathies, 308
spastic paraplegia, 138t
speech disturbance, 6, 7t
spherocytosis, hereditary, 359
spinal cord disorders
compression, 298, 298t
infections, 298
nerve root lesions, 298
subacute combined degeneration,
298–299
syringomyelia/syringobulbia, 299
splenectomy, 358
splenomegaly, 131
splinter haemorrhages, 14–15
spondyloarthropathies
ankylosing spondylitis, 338–339
enteropathic arthritis, 340
psoriatic arthritis, 339–340
reactive arthritis, 339
spontaneous pneumothorax, 219
primary, 219
spot diagnoses, 13, 13t
sputum, 4, 47, 50b
cytology, 215
squamous cell carcinoma, 154, 213, 354
stable angina, 170b
staphylococcal scalded skin syndrome, 157
Staphylococcus aureus, methicillin-
resistant, 382
statins, 170, 173–174, 315
status epilepticus, 289
ST elevation myocardial infarction
(STEMI), 171–172
STEMI. See ST-elevation myocardial
infarction (STEMI)
sternotomy scar, 17
steroids
asthma, 204–206t
COPD, 209
psoriasis, 349
rheumatoid arthritis, 337–338
Stevens-Johnson syndrome, 157, 353
stiffness, 8
Stokes-Adams attacks, 58, 112
stools, appearance of, 5
streptococcal infection, 196
Streptococcus pneumoniae, 296
stress incontinence, 94
stridor, 47–48
stroke, 283
Bamford classification, 124–125t
blood pressure control, 127b
causes and pathophysiology, 122
complications, 125t
differential diagnosis, 122b
examination, 123–125, 124f
history, 122–123
incidence, 121
investigations, 125–126
management, 126–127
prevention, 127
risk factors, 121b
symptoms and signs, 123f
types, 121t
strontium ranelate, 330
subacute thyroiditis, 110
subarachnoid haemorrhage, 101, 283
subcutaneous nodules, 152, 196
subdural haematoma, 102, 283–284, 284f
subtotal thyroidectomy, 317
sudden unexpected death in epilepsy
(SUDEP), 289
suicide risk, 385, 385b
sulphonylureas, 309–310
supraventricular arrhythmias, 175
antiarrhythmic drugs, 179–180
surgery
diabetic patients, 310–311
Paget disease, 332
rheumatoid arthritis, 337–338
splenectomy, 358
sweats, 3
swelling
abdominal, 6
ankle, 4
calf, 4
glandular, 8
joints, 8
Sydenham chorea, 196, 294
syncope, 4, 112. See also loss of consciousness
causes, 111t
syndrome of inappropriate secretion of
antidiuretic hormone (SIADH),
275, 276f, 277
causes of, 276–277, 276t
syphilis, 157, 272–273
syringobulbia. See syringomyelia
syringomyelia, 299
455

Index
systemic disease-related. See specific
conditions
systemic lupus erythematosus (SLE),
341–342
clinical features, 341, 341t
investigations, 341
pathology, 341, 341t
treatment, 341–342
systemic sclerosis
clinical features, 342, 342f, 343t
management, 342
pathology, 342
systems review, 3–8
cardiovascular symptoms, 4
gastrointestinal disease, 5–6
general symptoms, 3
genitourinary systems, 6
haematological symptoms, 8
metabolic and endocrine symptoms, 7
musculoskeletal symptoms, 7–8
neurological symptoms, 6
respiratory symptoms, 4–5
skin symptoms, 8
T
tapping, 17
tazarotene, 349, 349t
teichopsias, 284
temperature, sensory testing, 30, 31t
temporal arteritis, 102, 104b
temporal lobe, 290
tendons, 14
tenesmus, 5
tension pneumothorax, 219
tension-type headache, 102–103, 285
testicular cancer, 270
tetralogy of Fallot, 198–199
thalassaemia, 360–362
characteristics of, 360, 361t
clinical features, 360, 361t
management, 362
normal haemoglobin synthesis, 360,
360t
theophylline, 205, 206t
thiazide diuretics, 186–187
thiazolidinediones, 310
thigh pain, 4
thiopurine methyltransferase (TPMT),
239–240
third-degree heart block, 178
thrombin time (TT), 160
thrombocytopenia, 157, 162
thromboembolic disorders
aetiology, 372, 373t
clinical features, 372–373, 373t
haemolytic uraemic syndrome, 374
pathology, 372
risk factors, 372, 373t
thrombotic thrombocytopenic purpura,
374
treatment and prognosis, 373–374
456
thrombolysis, 127
thrombotic microangiopathies, 271–272
thrombotic thrombocytopenic purpura,
374
thrusting, 17
thyroid
enlargement, 34t
malignancy, 110
status, 35t
thyroid disease, 108–110
emergencies, 317
myxoedema coma, 317
thyrotoxic crisis, 317
hormone production control, 315, 316f
hyperthyroidism, 316
hypothyroidism, 316
management, 316–317
antithyroid drugs, 316–317
radioiodine, 317
subtotal thyroidectomy, 317
parathyroid disease, 317–319
thyroid lymphoma, primary, 110
thyroid storm. See thyrotoxic crisis
thyrotoxic crisis, 317
thyrotoxicosis, 109, 316. See also
hyperthyroidism
palpitations, 58
ticagrelor, 173
tinea, 153–154, 154f
tinnitus, 6
TNM classification, lung
cancer, 215, 216t
Todd paresis, 287
tonic-clonic seizures, 287
torsades de pointes, 177–178
total afferent pupillary defect, 24
toxic epidermal necrolysis, 157, 353
toxoplasmosis, 378, 379t
transient ischaemic attacks. See stroke
transient ischaemic attacks (TIAs), 283.
See also stroke
ABCD2 score for, 121t
causes and pathophysiology, 122
incidence, 121
transitional cell carcinoma, 269–270
transplantation, heart, 183
transthoracic echocardiogram, 169
Traube sign, 191
traumatic pneumothorax, 219
tremor, 28t
causes, 293, 293t
cerebellar, 293
essential, 293
Parkinson disease, 291
Treponema pallidum, 272–273
tricuspid regurgitation, 191
tricyclic antidepressants, 386t
overdose, 385, 386t
trigeminal nerve (V), 26, 26t
shingles, 102
trigeminal neuralgia, 102, 285
Troisier sign, 76
tropical sprue, 233
troponin, 172
tuberculosis (TB), 216–218
clinical features, 217–218
diagnostic tests, 218
extrapulmonary, 217–218
investigations, 218
management, 218
notification, 217t
pathogenesis, 217
pulmonary, 217–218
systemic, 217
tumours. See also specific tumours
skin, 354–355
skin manifestations, 347
tunnel vision, 23, 24t
two-point discrimination, sensory testing,
30, 31t
type I respiratory failure
causes, 201
management, 201–202
type II respiratory failure
causes, 202
management, 202–203
U
ulcer, 152t
ulcerated lesions, 157
ulcerative colitis
clinical features, 239
drug therapy, 239–240
investigations, 239
management, 239–240
prognosis, 240
surgical intervention, 240
Truelove and Witts classification, 239t
ultrasound
pleural effusion, 221
primary biliary cholangitis, 250
upper gastrointestinal tract, 229–234
gastroduodenal disorders, 230–232
oesophageal disorders, 229–230
small bowel disorders, 232–234
upper limbs
coordination, 29–30
muscle group movement, 29f
power, 29
reflexes, 30, 30f
sensation, 30
tone, 28
visual survey, 28
upper urinary tract infections, 267
urge incontinence, 94
urinalysis, 96
urinary symptoms
examination, 95–96, 95f
frequency, 6, 93
hesitancy, 6, 93
history, 94–95
incontinence, 6, 93
investigations, 96

Index
urinary tract infections (UTIs)
clinical features, 267–268
investigations, 267–268
lower urinary tract, 267
management, 268
upper urinary tract, 267
urinary tract malignancies
prostatic carcinoma, 270
testicular cancer, 270
transitional cell carcinoma, 269–270
urine
acute kidney injury, 257–258
appearance of, 6
glomerular disease, 264
proteinuria, 254
tests, 96
urticaria, 155
V
vaccines
influenza, 209
tuberculosis, 218
vaginal discharge, 6
vagus nerve, 28
valsalva manoeuvre, 177
valvular heart disease, 187–192
aortic regurgitation, 190–191
aortic stenosis, 190
mitral regurgitation, 189–190
mitral stenosis, 188–189
mitral valve prolapse, 190
pulmonary valve lesions, 191–192
tricuspid regurgitation, 191
vancomycin-resistant enterococci (VRE),
382
varicella. See herpes zoster
varices, 245
vasculitis
Behçet disease, 345
classification, 344–345, 344t
eosinophilic granulomatosis with
polyangiitis, 344
granulomatosis with polyangiitis, 344
Henoch-Schönlein purpura, 344–345
Kawasaki disease, 345
microscopic polyangiitis, 345
polyarteritis nodosa, 345
vasodilators, 187
vasopressin. See antidiuretic hormone
(ADH)
Venereal Disease Reference Laboratory
(VDRL) test, 272–273
venous thrombosis. See thromboembolic
disorders
ventricular arrhythmias, 175
antiarrhythmic drugs, 180
ventricular fibrillation (VF), 175, 178
ventricular hypertrophy, 184, 190,
193–194, 197–198
ventricular septal defect (VSD), 197
ventricular tachycardia, 177–178
verapamil, 173–174
for supraventricular arrhythmias,
179–180
vertebrobasilar insufficiency, 142t
vertigo, 6
aural symptoms, 143
characteristic features, 142t
differential diagnosis, 141, 141t
examination, 143–144, 144f
history, 142–143
indications, 144b
investigations, 144
neurological symptoms, 143
onset, 142
pattern, 142–143
vesicle, 152t, 154–155
vesicular lesions, 154–155
vessel wall abnormalities, 159, 163
vestibular disease, 27
vestibular neuronitis, 142t
vestibulocochlear nerve, 27
VIPomas, 234
viral hepatitis, 247
Virchow node, 76
visual acuity, 23
visual disturbance, 6
visual survey, clinical examination
cyanosis, 12
fluid status, 13
jaundice, 13
pallor, 12
patient position, 12
pigmentation, 13
vitamin B12, 357
vitamin D, 329, 329f
deficiency (see osteomalacia)
vitamin K deficiency, 162
vitiligo, 353
vocal fremitus, 50
vomiting, 5, 66
von Willebrand disease (vWD), 161, 371
Von Willebrand factor, 159
VRE. See vancomycin-resistant enterococci
(VRE)
vWD. See von Willebrand disease (vWD)
W
warfarin, 386t
overdose1, 2 (see coumarins)
water hammer, 191
weakness, 7–8
limb, 6
weepy/pustular lesions, 155
weight change, 3
weight loss
differential diagnosis, 85, 85t
examination, 86, 87f
history, 86
investigations, 86–87
Wells score algorithm, 373, 373t
Wernicke encephalopathy/Korsakoff
psychosis, 390–391
wheal, 152t
wheeze, 4, 48, 50
Whipple disease, 234
white-coat hypertension, 185
Wilson disease, 250–251
Wolff-Parkinson-White syndrome, 59, 177
writing in the medical notes, 37–40
X
xanthelasmata, 16
xanthomata, 14–15
Y
yellow nails, 14
Z
zidovudine, 378, 378f
zoledronic acid, 332
457
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