Musculoskeletal Flashcards

1
Q

Define giant cell arteritis

A

A form of vaculitis of large arteries. Granulomatous inflammation of external carotid artery and its branches, usually the temporal artery.

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2
Q

Summarise the aetiology of giant cell arteritis

A

Cause is unknown
Genetic and environmental factors contribute
Age and infectious agents may also have causative role
Associated with HLA-DR4 and HLA-DRB1

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3
Q

Summarise the epidemiology of giant cell arteritis

A

More common in those over 50
More common in females
25% of patients also have polymyalgia rheumatica
Most common systemic vasculitis in adults
Peak age of onset = 65-70 years old

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4
Q

What are risk factors for giant cell arteritis?

A
Age > 50 
Female 
Genetic Factors 
Smoking 
Atherosclerosis 
Environmental Factors
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5
Q

What are the presenting symptoms of giant cell arteritis?

A

Temporal headache with sensitivity on touching temporal region or brushing hair
Jaw claudication when eating
Visual symptoms - blurred vision, sudden blindness in one eye
Subacute onset

Systemic Symptoms: 
Malaise 
Low-grade fever 
Lethargy 
Weight loss 
Depression 

Symptoms of polymyalgia rheumatica:
Tenderness and stiffness of muscles of the shoulder and pelvic girdle
Early morning pain

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6
Q

What are the signs on physical examination of giant cell arteritis?

A

Palpable, thickened, non-pulsatile temporal artery
Absent temporal artery pulse
Abnormal fundoscopy
Swelling and erythema overlying the temporal artery
Temporal tenderness
Reduced visual acuity
Asymmetric blood pressure measurements

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7
Q

What are the appropriate investigations for giant cell arteritis?

A

Bloods:
CRP/ESR - raised
Hb and platelets are low
LFTs - transaminases and ALP slightly raised

Temporal artery biopsy - segmental giant cells (granulomas) in elastic - GRANULOMATOUS INFLAMMATION

Temporal artery ultrasound - thickening, stenosis or occlusion

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8
Q

What is the management of giant cell arteritis?

A

Immediately start high dose corticosteroids:
40-60mg PREDNISOLONE to prevent visual loss
After 5-7 days reduce steroid dose based off symptoms and ESR
Analgesia if needed
Osteoporosis prophylaxis - bisphosphonates, calcium, vit D
Low dose aspirin (+ PPIs and gastroprotection): reduces risk of visual loss, TIAs and stroke
Annual CXR for up to 10 years to look for thoracic aortic aneurysm

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9
Q

What are the possible complications of giant cell arteritis?

A

Aortic aneurysm
Irreversible visual loss due to optic nerve ischaemia
Large-vessel stenoses
Carotid artery aneurysm
Glucocorticoid related adverse effects i.e. DM and osteoporotic fractures

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10
Q

Summarise the prognosis of giant cell arteritis

A

Complete remission expected within 2 years
Patients respond quickly to treatment
Visual loss in treated patients is very rare
1-2 year treatment with glucocorticoids often needed

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11
Q

Define tension headache

A

The normal headache. A type of primary headache characterised by dull, pressing/tightening headache which can be chronic or episodic.
Chronic tension headaches = more than 15 headaches per month

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12
Q

Summarise the aetiology of tension headaches

A

Cause is unknown

Risk factors:
Mental Stress/Anxiety
Squinting/eye strain 
Poor Posture
Fatigue 
Dehydration 
Missing Meals
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13
Q

Summarise the epidemiology of tension headaches

A
Most common type of headache
Prevalence of 42% in adults
Most patients do not need treatment or are able to self-treat
Slightly more common in females
More common in young adults
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14
Q

What are the presenting symptoms of tension headache?

A

Dull, bilateral, tightening/pressing band-like headache
Non-pulsatile
Not worsened by daily activities
No nausea or autonomic symptoms
Photo/phonophobia present
Mild-moderate pain
Tenderness of muscles in the neck (i.e. trapezius muscles, SCM)
Gradual onset and variable duration
Usually responsive to over-the-counter medication

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15
Q

What are the signs on physical examination of tension headache?

A

No signs

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16
Q

What are the appropriate investigations for tension headaches?

A

Mainly clinical diagnosis therefore no investigations needed

Can consider:
CT Sinus: to exclude sphenoid sinusitis
MRI Brain: to exclude brain tumour
Lumbar Puncture: to exclude infective causes i.e. brain abscesses, meningitis

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17
Q

What is the management of a tension headache?

A

Analgesia:
Paracetamol
NSAIDs eg aspirin
Acetaminophen

Physical therapy if neck stiffness
Reassurance
Address triggers (e.g. stress, anxiety)
Advice on avoiding medications that can cause medication-induced headaches (e.g. opioids)

Chronic tension headache:
TCAs eg amitriptyline
Accupuncture

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18
Q

What are the possible complications of tension headaches?

A

NONE

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19
Q

What is the prognosis of tension headaches?

A

Self-treatment with simple analgesics is effective

Recurs but not severe or disabling

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20
Q

Define polymyalgia rheumatica

A

An immune-mediated inflammatory condition of unknown cause, which is characterised by severe bilateral pain and morning stiffness of the shoulder, neck and pelvic girdle.

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21
Q

Summarise the aetiology of polymyalgia rheumatica

A

Not well understood
Genetic and environmental factors
HLA-DR4 more likely
More likely following adenovirus or parvovirus B19 infection
Associated with temporal arteritis
- 40-50% of people with temporal arteritis have polymyalgia rheumatica
- 15% of people with polymyalgia rheumatica will develop temporal arteritis

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22
Q

Summarise the epidemiology of polymyalgia rheumatica

A
More common in women
More common in those above 50 years old
Associated with giant cell arteritis 
Incidence increases with age
Peak age of onset = 73 years old
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23
Q

What are the presenting symptoms of polymyalgia rheumatica?

A
Bilateral hip, shoulder and pelvic-girdle pain/aching/stiffness
Pain worse at morning on night
Pain improves with exercise
Difficulty standing up from chair or getting out of bed
Pain on lifting arms above shoulders
Fever
Fatigue
Loss of appetite
Weight loss
Symptoms >2 weeks

NO MUSCLE WEAKNESS

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24
Q

What are the signs on physical examination of polymyalgia rheumatica?

A

Bilateral arm tenderness
Bilateral shoulder and/or pelvic girdle pain
Bilateral shoulder and/or pelvic girdle stiffness

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25
What are the appropriate investigations for polymyalgia rheumatica?
Bloods: ESR/CRP - raised Muscle enzymes eg creatine kinase are normal Serum Protein electrophoresis: normal in polymyalgia rheumatica TFTs: TSH may be raised if hypothyroidism is the cause of symptoms Ultrasound - bursitis, joint effusions
26
What is the treatment of polymyalgia rheumatica?
Low dose corticosteroids - PREDNISOLONE - response within 24-72 hours Healthy diet Steroid-sparing agents (e.g. methotrexate) are sometimes used Calcium, vitamin D and bisphosphonates (Steroids can lead to osteoporosis) Assistance from physiotherapy and occupational therapy Monitor for adverse effects of steroids i.e. osteoporosis
27
What are the possible complications of polymyalgia rheumatica?
Giant cell arteritis Relapse Complications of corticosteroids: Osteoporosis - bone fractures Infection risk New onset T2DM
28
Summarise the prognosis of polymyalgia rheumatica
15% risk of getting temporal arteritis Variable course and prognosis Usually responds rapidly to steroid treatment Relapse is common
29
Define rheumatoid arthritis
An autoimmune mediated chronic, progressive inflammatory disorder of the joints, mainly those of the hands and feet. It is characterised by symmetrical deforming polyarthritis and extra-articular manifestations
30
Summarise the aetiology of rheumatoid arthritis
Unknown Genetic factors - HLA-DR1 and DR4 make it more likely Environmental factors - cigarette smoke, pathogen exposure Associated with other autoimmune conditions
31
Summarise the epidemiology of rheumatoid arthritis
1-2% of population Peak diagnosis in 50s Females more likely
32
What are the presenting symptoms of rheumatoid arthritis?
``` GRADUAL onset Joint pain (painful to touch and with range of motion exercises) Joint swelling Joint stiffness worse in the morning and worse with inactivity Impaired joint function Symmetrical joint involvement ``` Systemic Symptoms: Fever, Fatigue, Weight Loss, loss of appetite, muscle weakness In severe RA: Pleuritic chest pain due to pleural effusion Scleritis/uveitis Vasculitic Lesions (skin rashes)
33
What are the signs of rheumatoid arthritis on physical examination?
Most commonly in the HANDS and FEET Can affect shoulders, elbows, knees, ankles, wrists Affects more than 5 joints Spindling of fingers Swelling of MCP, PIP and MTP Joints Tender joints Reduction in range of movement ``` Late Signs Ulnar deviation of fingers Radial deviation of the wrist Swan neck deformity Boutonniere deformity Z deformity of the thumb ``` Rheumatoid nodules (firm subcutaneous nodules) on elbows, palms, over extensor tendons Baker's cyst development
34
What are the appropriate investigations for rheumatoid arthritis?
Clincal diagnosis ``` Bloods: FBC - anaemia, leukocytosis, thrombocytosis ESR/CRP - raised Rheumatoid factor positive Anti-CCP antibody positive ``` ``` X-ray: Decreased bone density around joint Soft tissue swelling Decreased joint space Bony erosions ``` Joint aspiration - rule out septic arthritis
35
Define osteoarthritis
Age-related degenerative synovial joint disease when cartilage destruction exceeds repair, causing pain and disability.
36
Summarise the aetiology of osteoarthritis
Exact aetiology is unknown Secondary Osteoarthritis - Other diseases lead to altered joint architecture and stability Commonly associated diseases include: Developmental abnormalities (e.g. hip dysplasia) Trauma (e.g. previous fractures) Inflammatory (e.g. rheumatoid arthritis, gout, septic arthritis) Metabolic (e.g. haemochromatosis, acromegaly) ``` Risk factors: Age Inflammation Joint injury Obesity Mechanical stress Neurologic disorders Female Post-menopause Genetics Medications High bone mineral density ```
37
Summarise the epidemiology of osteoarthritis
Common in those over 50 years old Very common Common in women and more common as age increases More common in Asians and Caucasians
38
What are the presenting symptoms of osteroarthritis?
Joint stiffness in the morning for less than an hour and in the evening Joint pain worse with activity Sharp, aching, burning joint pain NO JOINT SWELLING Limited range of movement Functional difficulties Stiffness and gelling after inactivity for a few minutes
39
What are the signs on physical examination of osteoarthritis?
``` Local joint tenderness Crepitus and pain during joint movement Joint effusion Restriction of range of joint movement Antalgic gait (gait to avoid pain) ``` Bony swellings along joint margins: Heberden's Nodes: DIP joint Bouchard's Nodes: PIP joint
40
What are the appropriate investigations for osteoarthritis?
``` X-ray of affected joints: Loss of joint space Subchondral sclerosis Osteophytes Subcondral cysts ``` Bloods: Serum ESR/CRP - normal Rheumatoid factor - distinguish between osteoarthritis and rheumatoid - NEGATIVE Anti-CCP antibody - distinguish between osteoarthritis and rheumatoid - NEGATIVE
41
Define septic arthritis
The infection of 1 or more joints by pathogenic inoculation of microbes by either direct inoculation or haematogenous spread.
42
Summarise the aetiology of septic arthritis
In most cases there is systemic infection allowing for haematogenous spread Gonnococcal arthritis caused by neisseria gonorrhoaea is a minority and expected in sexually active adolescents Most common is STAPHYLOCOCCUS AUREUS Gram negative bacteria more common in old and immunocompromised Common causative organisms: Bacteria All ages: Staphylococcus aureus, TB < 4 years: Streptococcus pneumoniae, Streptococcus pyogenes, Neisseria meningitidis 16-40 years: Neisseria gonorrhoeae Viruses: Rubella, Mumps, Hepatitis B, Parvovirus B19 Fungi: Candida
43
Summarise the epidemiology of septic arthritis
6 cases per 100,000 per year Incidence increases in those with underlying joint disease or prosthetic joints Most common in children and elderly
44
What are the risk factors for septic arthritis?
``` Recent orthopaedic procedures Osteomyelitis Diabetes Immunosuppression Alcoholism Underlying joint disease Joint prostheses IV drug use ```
45
What are the presenting symptoms of septic arthritis?
Red, swollen, warm joint Painful joint - EXCRUCIATING Restricted range of movement Fever Usually a monoarthropathy (usually affecting one large joint) May cause a polyarthropathy in the immunosuppressed Tuberculous arthritis develops more slowly and is more chronic
46
What are the signs on physical examination of septic arthritis?
Painful, hot, swollen and immobile joint Erythema Severe pain prevents passive movement Pyrexia
47
What are the appropriate investigations for septic arthritis?
``` JOINT ASPIRATION AND ANALYSIS OF OBTAINED SYNOVIAL FLUID - MC&S: Purulent aspirate High white cell count Positive gram stain or culture PCR of aspirate if expect viral cause ``` ``` Bloods: FBC: high WCC, high neutrophils CRP/ESR: High Blood cultures - MC&S Viral serology may be useful ``` Plain Joint Radiographs: Affected joint can show signs of damage following the infection Joint USS - may show presence of joint effusion MRI Scan: Useful for detecting osteomyelitis
48
Define carpal tunnel syndrome
A nerve entrapment disorder causing signs and symptoms due to compression of the median nerve, often resulting in tingling, pain and parasthesia of the lateral 3 and a half fingers.
49
Explain the aetiology of carpal tunnel syndrome
It is caused by compression of the median nerve. This can occur from any inflammation of nearby tendons and tissues, leading to oedema. Overuse/repetitive stress injury can cause Usually idiopathic Can be secondary to: Tenosynovitis - rheumatoid arthritis Infiltrative diseases of the canal/soft tissue - amyloidosis, acromegaly Bone involvement in the wrist - osteoarthritis, fracture Fluid retention states - pregnancy, nephrotic syndrome Obesity Menopause Diabetes
50
What are the risk factors of carpal tunnel syndrome?
``` Obesity Pregnancy Diabetes mellitus Hypothyroidism Rheumatoid arthritis Fractured wrist Female Increased age ```
51
Summarise the epidemiology of carpal tunnel syndrome
3 times more common in females Most common in 40-60 year olds 1 in 25 people Most common entrapment neuropathy
52
What are the presenting symptoms of carpal tunnel syndrome?
Numbness (parasthesia) in lateral 3 and a half digits Pain in lateral 3 and a half digits Dull ache over lateral 3 and a half digits Tingling/burning over lateral 3 and a half digits Muscle weakness Clumsiness - difficulty with fine motor tasks eg doing buttons, turning keys, holding small objects Symptoms worse at night Aching and pain in forearm Gradual onset in symptoms Cold sensitivity
53
What are the signs on physical examination of carpal tunnel syndrome?
Sensory impairment in the median nerve distribution Thenar muscle wasting and weakening Phalen's maneuvre - flexing the wrist as far as possible and holding for a minute causing reproduction of symptoms Tinel's sign - tapping over the flexor retinaculum causes symptoms
54
What are the appropriate investigations for carpal tunnel syndrome?
EMG - slowing of conduction velocity in median sensory nerves across the carpal tunnel USS/MRI wrist - may show space occupying lesion
55
Define reactive arthritis
A type of seronegative spondlyarthropathy. Inflammation of joints following a genitourinary or gastrointestinal infection
56
What is the triad of Reiter's syndrome?
Reactive arthritis Urethritis Conjunctivitis
57
Summarise the aetiology of reactive arthritis
Associated with HLA-B27 Often following genitourinary infection eg chlamydia (most common) or gastroenteritis eg salmonella, shigella, yersinia, campylobacter, e. coli GRAM NEGATIVE CAUSATIVE ORGANISMS
58
Summarise the epidemiology of reactive arthritis
Much more common in males Affects adults Age of onset: 20-40 years Seen in 2% of patients with non-specific urethritis
59
What are the presenting symptoms of reactive arthritis
Preceding urogenital or gastroenteritis 2-4 weeks previously Pain and swelling of single large joint Painful, stinging on urination if urethritis Red, painful eye if conjunctivitis Dyspareuria if cervicitis Chest pain and fever if pericarditis Low back pain (due to sacroiliitis) Painful heels (due to enthesitis and plantar fasciitis) Skin Rash Penile Ulcer Constitutional symptoms: Fever, Fatigue and Weight Loss
60
What are the signs on physical examination of reactive arthritis?
Asymmetrical oligoarthritis Affects the larger joints in lower extremities Tender, swollen, warm, red and stiff joints Dactylitis: Sausage-shaped digits Conjunctivitis and Anterior uveitis Circinate balanitis: Scaling red patches on the glans penis ``` Keratoderma Blennorrhagica: Brownish-red macules Vesicopustules Yellowish-brown scales Found on the SOLES and PALMS ``` ``` Aortitis: This can cause aortic regurgitation which can precipitate heart failure Oral Ulceration (usually painless) Nail dystrophy Hyperkeratosis Onycholysis ```
61
What are the appropriate investigations of reactive arthritis?
FBC - anaemia suggests severe systemic illness ESR/CRP - high HLA-B27 testing - positive ANA and Rheumatoid factor - NEGATIVE (to rule out differentials) Stool or Urethral Swabs and Cultures - may be negative by the time the arthritis develops Urine Screen for Chlamydia trachomatis Plain X-Rays: Chronic cases Erosions seen at the entheses (insertion of tendons into bone) Sacroiliitis Arthrocentesis with synovial fluid analysis - exclude crystal induced arthritis such as gout
62
Define gout
An syndrome characterised by hyperuricaemia and deposition of urate crystals into soft tissue and joint, resulting in recurrent bouts of acute inflammatory monoarthropathy, often affecting the big toe.
63
Summarise the aetiology of gout
Caused by hyperuricaemia and deposition of monosodium urate crystals in the joint Decreased excretion of uric acid - 90% - Idiopathic - Renal failure - Medication eg thiazide diuretics Overproduction of purines - Consumption of purine-rich food (shellfish, red meat) - Increased nucleic acid turnover (e.g. lymphoma, leukaemia, psoriasis) - Increased synthesis of urate Genetic predisposition Chemotherapy/radiotherapy causing tumour lysis syndrome ``` Drugs causing gout = CAN'T LEAP Ciclosporin Alcohol Nicotinic acid Thiazides Loop diuretics Ethambutol Aspirin Pyrizinamide ```
64
What are the risk factors of gout?
``` Male Alcohol Diabetes/insulin resistance Hypertension Obesity Dyslipidaemia Increasing age Renal insufficiency Consumption of Meat Seafood and alcohol ‘CANT LEAP’ Drugs Genetic Susceptibility High cell turnover rate ```
65
Summarise the epidemiology of gout
Incidence increases with age More common in men - male to female ratio 7:1 Prevalence of 1% Very rare pre-puberty and in pre-menopausal women More common in HIGHER social classes
66
What are the presenting symptoms of gout?
``` Precipitating factors: Alcohol Red meat intake Increased thiazide diuretic dose Trauma Infection Introduction or withdrawal of hypouricemic agents ``` ``` Sudden onset severe pain Swollen, red, erythematous, warm joint Often metatarsolphalangeal joint of big toe Joint stiffness Monoarticular - few joints affected Tender Pain wakes them up from sleep Joint feels like it is on fire ``` Symptoms peak at 24 hours and resolve over 7-10 days Asymptomatic by monoarticular arthritis pain
67
What are the signs on physical exmamination of gout?
Erythematous, oedematous warm joint which is tender to light palpation Limited joint movement Tophi in external ear, olecranon, achilles tendon, toe Fever
68
What are the appropriate investigations in gout?
Serum uric acid - hyperuricaemia Urine uric acid CRP/ESR - elevated WCC - elevated Synovial joint aspiration: Increased WBCs with neutrophil predominance Monosodium urate crystals Synovial fluid polarised light microscopy: Negative bifringence Sharp needle shaped deposits - yellow under parallel light, blue under perpendicular light X-Ray: Crystal deposits, Periarticular erosions USS (erosions, tophi, double contour line) AXR/KUB Film: Uric acid renal stones may be seen - increased risk of nephrolithiasis
69
Define psuedogout
Arthritis associated with calcium pyrophosphate dihydrate crystal deposition in joint cartilage.
70
Summarise the aetiology of pseudogout
Caused be deposition of calcium pyrophosphate crystals in joint cartilage Often idiopathic ``` It is associated with: Hyperparathyroidism Hypothyroidism Haemochromatosis Trauma Hypomagnesemia Hypophosphataemia ``` Precipitating factors: Intercurrent illness, Surgery, Local trauma
71
Summarise the epidemiology of pseudogout
Increasing incidence with age More common >60 More common in females
72
What are the presenting symptoms of pseudogout?
``` Painful, swollen, red, warm joint Affects >1 joint Often large joint such as knee Reduced joint mobility Fever and malaise Sudden worsening of osteoarthritis ```
73
What are the signs on physical examination of pseudogout?
Acute Arthritis: Red, hot, tender, swollen joints Restricted range of movement (esp. shoulders, wrists, MCP Joints) ``` Chronic Arthropathy: Similar to osteoarthritis Bony swelling Crepitus Deformity Restriction of movement ```
74
What are the appropriate investigations of pseudogout?
WCC and ESR - elevated Synovial fluid analysis: See rhomboid or rod-shaped calcium pyrophosphate crystals Crystals show positive bifringence X-Ray: chondrocalcinosis, signs of osteoarthritis (Loss of Joint space, Osteophytes, Subchondral cysts, Sclerosis) Exclude other causes: Serum calcium - exclude hyperparathyroidism Serum PTH - exclude hyperparathyroidism Iron studies - exclude haemochromatosis Serum magnesium - exclude hypomagnesaemia Serum ALP - exclude hypophosphatasia
75
Define fibromyalgia
Chronic pain disorder in mainly middle aged females characterised by widespread muscle pain, increased tenderness, decreased pain threshold and mood and sleep disturbances.
76
Summarise the aetiology of fibromyalgia
Aetiology is unknown Thought to be due to problem with pain perception in brain Genetic impact as often runs in families Environmental impact - common in those who experienced child abuse ``` Risk factors: Female Family history of fibromyalgia Age 20-60 Rheumatological condition ```
77
Summarise the epidemiology of fibromyalgia
Most common in middle aged women | Average age of presentation is 35 years old
78
What are the presenting symptoms of fibromyalgia?
``` Widespread musculoskeletal pain with associated stiffness Morning stiffness Increased tenderness Headaches Fatigue which is unrelieved by sleep Sleep disturbance Mood disturbance Cognitive disturbance - concentration, memory Hypersensitivity to light, noise, smell Parasthesia Tingling and numbness Fluid retention ``` Symptoms occuring for >3 months
79
What are the signs on physical examination of fibromyalgia?
Normal physical examination with increased tenderness
80
What are the appropriate investigations for fibromyalgia?
Mainly a clinical diagnosis Tenderness in 11 out of out of 18 points Widespread pain on both sides of body, above and below waist for at least 3 months Pain location >7 areas with symptom severity >5/12 ``` Investigations to exclude other cause: FBC - exclude anaemia, iron deficiency TFT - exclude hypothyroid RF and anti-CCP - exclude rhuematoid arthritis ESR/CRP ANA - exclude SLE ```
81
Define ankylosing spondylitis
A seronegative spondyloarthropathy, characterised by axial spine involvement, inflammatory back pain, sacroiliitis and vertebral fusion.
82
Summarise the aetiology of ankylosing spondylitis
Aetiology unknown Autoimmune condition however no associated auto-antibodies Associated with HLA-B27 Infective triggers and antigen cross-reactivity with self-peptides have been hypothesised Associated with family history Pathophysiology: Inflammation starts at the entheses (where ligaments attach to vertebral bodies) Persistent inflammation leads to reactive new bone formation Changes begin in the lumbar vertebrae and progress superiorly
83
Summarise the epidemiology of ankylosing spondylitis
Most common in young men Usually presents in 20s Men present earlier
84
What are the presenting symptoms of ankylosing spondylitis?
Lower back pain - worse in morning or when resting, relieved by exercise, insidious onset, wakes up from sleep Limited range of movement of back Inflammed and painful tendons Buttock pain due to sacroiliitis Symptoms of Iritis/Uveitis: redness, discomfort, photophobia Pleuritic Chest Pain, Dyspnoea (due to costovertebral joint involvement) Heel Pain (due to plantar fasciitis) Malaise, Fatigue
85
What are the signs on physical examination of ankylosing spondylitis?
Reduced range of spinal movement: hip rotation and lateral spinal flexion Tenderness over sacroiliac joints Loss of lumbar lordosis - QUESTION MARK POSTURE Schober’s Test: Two fingers placed on back 10cm apart Patient bends over Normal = distance between fingers increases by >5cm Reduced movement would suggest ankylosing spondylitis Thoracic kyphosis Spinal fusion ``` Signs of Extra-Articular Disease: 5 As Anterior Uveitis Apical lung fibrosis Achilles Tendonitis Amyloidosis Aortic Regurgitation ``` Signs and symptoms of IBD
86
What are the appropriate investigations of ankylosing spondylitis?
MRI spine - early = joint space narrowing and erosion, later = spine fusion Pelvic X-ray - scaroiliitis X-Ray spine - bamboo spine (fusion of vertebrae) CRP/ESR - elevated Genetic testing - HLA-B27 positive CXR: Check for apical lung fibrosis Lung Function Tests: assess mechanical ventilatory impairment due to kyphosis
87
Define osteomyelitis
Inflammed bone or bone marrow, usually due to infection most commonly by staphylococcus aureus. It leads to inflammation and necrosis of bone and formation of new bone and can be acute or chronic.
88
Summarise the aetiology of osteomyelitis
Can be caused by haematogenous spread from bacteraemia, direct innoculation due to trauma or surgery, contiguous spread from an adjacent area Most common causative agent is staphylococcus aureus In IVDU - psuedomonas can affect In sickle cell - salmonella can affect In neonates - group B strep and E.coli can affect ``` Risk Factors: Diabetes Immunosuppression IV drug use Prostheses Sickle-cell anaemia ```
89
Summarise the epidemiology of osteomyelitis
More common in children 2-12 years old | 3 times more common in boys
90
What are the presenting symptoms of osteomyelitis?
``` Pain at site of infection Fever/rigors Fatigue Swelling of area Redness at area Reduced movement of affected area Malaise History of preceding skin lesion, sore throat, trauma or operation ```
91
What are the signs on physical examination of osteomyelitis?
``` Erythema Tenderness Warm Swollen joint Reduced range of movement Sero-purulent discharge from an associated wound or ulcer ```
92
What are the appropriate investigations for osteomyelitis?
``` FBC - elevated WBC ESR/CRP - elevated Blood culture Bone biopsy and culture X-ray - radiolucency, soft tissue swelling, osteopenia Swabs of wound or discharge ```
93
Define cervical spondylosis
Progressive degenerative process affecting the cervical vertebral bodies and intervertebral discs and causing compression of the spinal cord and/or nerve roots.
94
Summarise the aetiology of cervical spondylosis
Osteoarthritic degeneration of the vertebral bodies leads to the formation of osteophytes These osteophytes protrude on to the foramina and spinal canal This leads to compression of: Nerve roots: radiculopathy Anterior spinal cord: myelopathy Risk Factors: Older Age > 40, Obesity, Previous Trauma, Poor Posture, Inactivity
95
Summarise the epidemiology of cervical spondylosis
Mean age at diagnosis = 48 years old | More common in males
96
What are the presenting symptoms of cervical spondylosis?
``` Neck pain/stiffness Arm pain (stabbing or dull ache) Atypical chest pain Breast pain Pain in the face Pins and needles and/or paraesthesia ``` ``` Spinal stenosis (severe disease): Lack of coordination/clumsiness of hands i.e. buttoning a shirt Heaviness or weakness in arms or legs Problems walking (gait disturbance) Problems controlling bladder and bowel ```
97
What are the signs on physical examination of cervical spondylosis?
ARMS: Atrophy of the forearm and hand muscles Segmental muscle weakness in a nerve root distribution Hyporeflexia Sensory loss (mainly pain and temperature) Pseudo athetosis (writhing finger movements when hands are outstretched, fingers spread, and eyes closed) ``` LEGS – if cervical cord compression: Increased tone Weakness Hyperreflexia Extensor plantar response Reduced vibration and joint position sense ``` Lhermitte's Sign: neck flexion causes crepitus (grating sound) and/or paraesthesia down the spine
98
What are the appropriate investigations for cervical spondylosis?
Spinal X-ray (lateral) - Can detect osteoarthritis change | MRI - Allows exclusion of root and cord compression, exclude spinal cord tumour and nerve root infiltration