MSK Flashcards

(295 cards)

1
Q

What are the 3 conditions making up the seronegative spondyloarthropathies?

A

Ankylosing spondylitis
Psoriatic arthritis
Reactive arthritis

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2
Q

What joints are mainly affected in ankylosing spondylitis?

A

Vetebral column joints
Sacroiliac joints

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3
Q

What gene is associated with ankylosing spondylitis

A

HLA-B27

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4
Q

What is the typical presentation of ankylosing spondylitis

A

Young adult male in their 20s with:
Pain and stiffness in the lower back
Sacroiliac pain

Pain and stiffness is worse in the morning and takes around 30 mins to improve, improves with exercise and worsens with rest

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5
Q

What symptoms can one experience other than back and sacroiliac pain in ankylosing spondylitis

A

Chest pain related to the costovertebral and sternocostal joints
Enthesitis (inflammation of the entheses, where tendons or ligaments insert into bone)
Dactylitis (inflammation of the entire finger)
Vertebral fractures (presenting with sudden-onset new neck or back pain)
Shortness of breath relating to restricted chest wall movement)

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6
Q

What conditions are associated with ankylosing spondylitis

A

5A’s
Anterior uveitis
Aortic regurgitation
Atrioventricular block
Apical lung fibrosis
Anaemia of chronic disease

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7
Q

Investigations for anklyosing spondylitis

A

Schober’s test - mark 10cm above and 5cm below L5 vertebrae and ask patient to bend forward –> length of <20cm between points = supportive of anklyosing spondylitis
ESR/CRP
HLA-B27 gene testing
X-ray of spine and sacrum
MRI of spine

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8
Q

What would an X-ray show in anklyosing spondylitis

A

Sacroiliitis: subchondral erosions, sclerosis
Squaring of lumbar vertebrae
‘bamboo spine’ (late & uncommon)
Syndesmophytes: due to ossification of outer fibers of annulus fibrosus

Apical fibrosis in CXR

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9
Q

What would an MRI of show in ankylosing spondylitis

A

Bone marrow oedema in sacroiliac joints

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10
Q

Management of ankylosing spondylitis

A

Regular exercise
1st line = NSAIDs
Anti-TNF therapy (if high disease activity) - adalimumab, etanercept or infliximab
Physiotherapy

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11
Q

What is the function of bursae

A

They act to reduce the friction between the bones and soft tissues during movement.

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12
Q

What are the causes of bursitis

A

Friction from repetives movement or leaning on the elbow
Trauma
Infection - septic bursitis
Inflammatory conditions - rheumatoid arthritis or gout

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13
Q

What are the symptoms of olecranon bursitis

A

Young/middle-aged man with an elbow that is:
Swollen
Warm
Tender
Fluctuant (fluid filled)

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14
Q

How do you identify that bursitis is caused by infection

A

Hot to touch
More tender on plapation
Erythema spreading to surrounding skin
Fever
Skin abrasion overlying the bursa
Features of sepsis - tachycardia, hypotensions, confusion)

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15
Q

Investigations for olecranon bursitis

A

Clinical diagnosis
If infection suspected:
Aspiration of bursal fluid and examine fluid:
Pus = infection
Straw-coloured = infection less likely
blood stained = trauma, infection or inflammatory cause
Milky = gout or psuedogout

Microscopy and culture of fluid:
Gram staining for bacteria
Examine for crystals = gout/pseudogout

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16
Q

Management of olecranon bursitis

A

Rest
Ice
Compression
Analgesia (e.g., paracetamol or NSAIDs)
Protecting the elbow from pressure or trauma
Aspiration of fluid may relieve pressure
Steroid injections may be used in problematic cases where infection has been excluded

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17
Q

Treatment of olecranon bursitis due to infective cause

A

Aspiration for microscopy and culture
Antibiotics - flucloxacillin (2nd line = clarithromycin)

IF septic = sepsis 6

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18
Q

Presentation of trochanteric bursitis

A

Middle aged patient with:
Gradual onset hip pain (over greater trochanter) - aching or burning
May radiate down the outer thigh
Worse with activity, standing after sitting and trying to sit cross legged
Tenderness over geeater trochanter

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19
Q

What would be the examination finding in trochanteric bursitis

A

Positive Trendelenburg test
Resisted abduction of the hip
Resisted internal rotation of the hip
Resisted external rotation of the hip

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20
Q

What is the Trendelenburg test

A

Involves asking the patient to stand one-legged on the affected leg. Normally, the other side of the pelvis should remain level or tilt upwards slightly. A positive Trendelenburg test is when the other side of the pelvis drops down, suggesting weakness in the affected hip.

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21
Q

Management of trochanteric bursitis

A

Rest
Ice
Analgesia (e.g., ibuprofen or naproxen)
Physiotherapy
Steroid injections

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22
Q

Define compartment syndrome

A

Where the pressure within a fascial compartment is abnormally elevated, cutting off the blood flow to the contents of that compartment

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23
Q

If compartment syndrome is not treated in time what can occur

A

Tissue necrosis

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24
Q

Where does compartment syndrome most commonly affect

A

Leg
Forearm
Feet
Thigh
Buttocks

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25
What is the presentation of compartment syndrome
Usually after an acute injury like: Bone fracture Crush injuries Presentation: 5 P's Pain - disproportionate to underlying injury (not made better with analgesics) and made worse by stretching Parathesia Pale Pressure (high) Paralysis (a late and worrying feature)
26
Investigations for compartment syndrome
Needle manometry - Pressures >20mmHg is abnormal and >40mmHg is diagnostic
27
Management of compartment syndrome
Initial: Removing any bandages/dressing Elevation of leg Maintaing good BP (avoid hypotension) Emergency fasciotomy - cutting the fascia to release pressure - Debridement of any necrotic tissue too
28
What are patients undergoing fasciotomy due to compartment syndrome at risk of and what is given to avoid this
Myoglobinuria - myoglobin released from dead RBCs and enters blood stream where it reaches kidneys and excreted Breakdown of myoglobin can damage kidney Patient given aggressive IV fluids to prevent this
29
What is chronic compartment syndrome
Usually due to exertion During exertion, the pressure within the compartment rises, blood flow to the compartment is restricted, and symptoms start. During rest, the pressure falls, and symptoms begin to resolve. It is not an emergency. Same treatment and symptoms as acute
30
What are the two types of crystal arthropathies
Gout Pseudogout
31
What is gout
Chronically high blood uric aci levels with urate crystals deposited in the joints causing them to become inflamed
32
What are the risk factors for gout
Male Family history Obesity High purine diet (meat and seafood) Alcohol Diuretics Cardiovascular disease Kidney disease
33
What joints are mostly affected in gout
Metatarsophalangeal joint (base of big toe) Carpometacarpal joint (base of thumb) Knee Ankle
34
What are the symptoms of gout
Acute - develop meaximal intesnsity within 12 hours: Pain of the joint Swelling of the joint Erythema of the joint
35
Investigations for gout
Uric acid levels: - Above 360umol/L = gout strongly suspected Synovial fluid analysis from joint aspiration shows: Monosodium urate crystals Needle shaped crystals Neatively birefringent under polarised light
36
What can gout show on X-rays
Lytic lesions Punched out erosions Erosions have sclerotic borders with overhanging edges Joint effusion
37
Management of gout
Acute flares: 1st line = NSAIDs (with PPIs) 2nd line = colchicine 3rd line = steroids (prednisolone) Prophylaxis: Allopurinol Febuxostat (once allopurinol is started, continue it even during another acute attack as well as taking meds for acute flares) Lifestyle changes: No alcohol Minimising purine diet
38
What is pseudogout caused by
Deposition of calcium pyrophosphate dihydrate crystals in the synovium
39
Presentation of pseudogout
Joint is: Hot Swollen Stiff Painful
40
What joints does pseudogout affect
Knee (most common) Shoulders Hips Wrists
41
Investigations for pseudogout
Joint aspiration shows: Calcium pyrophoshpate crystals Rhomboid shaped crytals Positively birefringent of polarised light X-ray
42
What does an x-ray show in pseudogout
Chondrocalcinosis - calcium deposits in the joint cartilage show up in a thin white line in the middle of the joint space. LOSS Loss of joint space Osteophytes (bone spurs) Subarticular sclerosis (increased density of the bone along the joint line) Subchondral cysts (fluid filled holes in the bones)
43
Management of pseudogout
NSAIDs (with PPIs) Colchicine Intra-articular steroid injections Oral steroids
44
What is fibromyalgia
Widespread pain throughout the body with tender points at specific anatomical sites
45
Typical presentation of fibromyalgia
Women between 30 and 50 with: Chronic pain at multiple sites, sometimes pain all over Lethargy Cognitive impairment (fibro fog) Sleep disturbances Headaches Dizziness
46
Investigations for fibromyalgia
History of widespread pain Pain must be present at 11 of the 18 tender point sites published by American College of Rheumatology classification criteria
47
Management of fibromyalgia
Aerobic exercise CBT Pregabalin Duloxetine Amitriptyline
48
What are the risk factors for osteoarthritis
Female Obese Age Occupation Trauma Family history
49
What are the most common sites for osteoarthritis
Hips Knees Distal interphalangeal joints (DIP) in the hands Carpometacarpal (CMC) joint at base of thumb Lumbar spine Cervial spine (cervial spondylosis)
50
Pathophysiology of osteoarthritis
Imbalance between cartilage damage and the chondrocyte response
51
Presentation of osteoarthritis in the hands
Usually bilateral Episodic aching pain provoked by movement and relieved by rest Stifness Painless nodes: Bouchard's nodes - PIPJs Heberden's nodes - DIPJs Squaring of the base of thumbs Weak grip
52
Presentation of osteoarthritis in the hip
Chronic history of aching groin pain following exercise and relieved by rest
53
Investigations for osteoarthritis
Clinical if typical features X-ray shows LOSS: Loss of joint spcae Osteophytes Subchondral sclerosis Subchondral cysts
54
Management of osteoarthritis
Weight loss advice, local muscle strengthening exercises 1st line = topical NSAIDs 2nd line = oral NSAIDs (PPI co-prescribed) IF above do not work then: Intra-articular injections (last for 2-10 weeks) If all do not work then: Joint replacement
55
What are the adverse affects of long term NSAIDs use
GI side effects - gastritis, peptic ulcers Renal - AKI (acute tubular necrosis) and CKD Cardio - hypertension, heart failure, MI, stroke Exacerbating asthma
56
What is osteomalacia
Soften bones caused by insufficient Vitamin D
57
What does Vitamin D help absorb
Helps absorb Calcium and Phosphate in the intestines and kindeys
58
Why may patients with osteomalacia get secondary hyperparathyroidism
Decreased Vitamin D = insufficient Calcium and Phosphate absorption = increased PTH released = secondary hyperparathyroidism
59
Causes of osteomalacia
Vitamin d deficiency: - malabsorption - lack of sunlight - diet CKD Durg induced - anti-convulsants Liver disease = cirrhosis Coeliac disease Inherited: hypophosphatemic rickets (previously called vitamin D-resistant rickets)
60
Presentation of osteomalcia
Fatigue Bone pain Muscle pain Muscle aches Pathological or abnormal fractures Proximal myopathy - waddling gait
61
Investigations for osteomalacia
Serum 25-hydroxyvitamin D (VItamin D) = low Serum calcium = Serum phosphate = low Serum alkaline phosphatase = high PTH = high (secondary hyperparathyroidism)
62
What will X-rays show in osteomalacia
Translucent bands (Looser's zones or psuedofractures) Looser zones are fragility fractures that go partially through the bone
63
Management of osteomalacia
Vitamin D supplementation (loading dose is often needed) Calcium supplementation if dietary calcium is inadequate
64
Why does NICE recommend testing serum calcium a month after loading dose of Vitamin D
NICE CKS (2022) recommend checking the serum calcium within a month of the loading regime. It may be: Low in calcium deficiency High in primary hyperparathyroidism (previously masked by the vitamin D deficiency) High in other conditions that cause hypercalcaemia, such as cancer, sarcoidosis or tuberculosis
65
What is osteomyelitis
Refers to inflammation in a bone and bone marrow
66
What are the two main ways somoene can acquire osteomyelitis
Haematogenous osteomyelitis = pathogen is carried through the blood and seeded in the bone Non-haematogenous spread - due to direct contamination of the bone, for example, at a fracture site or during an orthopaedic operation
67
What organism most commonly causes osteomyelitis
Staphylococcus aureus
68
Risk factors for osteomyelitis
Open fractures Orthopaedic operations (specifically with prosthetic joints) Diabetes (particularly with diabetic foot ulcers) Peripheral arterial disease IV drug use Immunosuppression
69
Presentation of osteomyelitis
Fever Pain and tenderness around site of infection Erythema around site of infection Swelling around site of infection Muscle aches Lethargy
70
Investigations for osteomyelitis
Bloods: Raised WCC, ESR, CRP Blood cultures - identify causative organism MRI Bone cultures
71
Management of osteomyelitis
6 weeks of flucloxacillin (clindamycin for penicllin allergy) - possibly with rifampicin or fusidic acid IF MRSA: vancomycin or teicoplanin IF associated with prosthetic joints then: complete revision surgery to replace prosthesis
72
Treatment of chronic osteomyelitis
3 or more months of antibiotics
73
What is paget's disease of bone
Excessive bone turnover (reabsorption and formation) due to increased osteoclast and osteoblast activity
74
Where does paget's disease most commonly affect
Axial skeleton: Spine Skull
75
Risk factors for paget's disease of bone
Male Increasing age Family history Northern latitude
76
Presentation of paget's disease of bone
Bone pain (e.g. pelvis, lumbar spine, femur) Bone deformity - bowing of tibia and/or bossing of skull Fractures Hearing loss
77
Investigations for paget's disease of bone
Bloods: Raised ALP Normal calcium and phosphate X-ray Bone scintigraphy - increased uptake is seen focally at the sites of active bone lesions
78
What are the X-ray findings in paget's disease of bone
Bone enlargement and deformity Osteoporosis circumscripta (well-defined osteolytic lesions that appear less dense compared with normal bone) Cotton wool appearance of the skull (poorly defined patchy areas of increased and decreased density) V-shaped osteolytic defects in the long bones
79
What is the management of paget's disease of bone? What are the aims of treatment?
Aims: - Eliminate bone pain - Normalise serum alkaline posphatase Bisphosphanates - oral risendronate Calcitonin Analgesia
80
Complications of paget's disease of bone
Fractures Hearing loss (affects bones in the ear) Heart failure (due to hypervascularity of abnormal bone) Osteosarcoma Spinal stenosis = spinal canal narrowing = cord compression = nuerological symtpoms
81
What are the features of polymyalgia rheumatica
Usually rapid onset (< 1 month) Aching and morning stifness in proximal muscles - neck, shoulders and hips Worse in the morning, after rest or inactivity Inteferes with sleep Improves with activity
82
Investigations for polymyalgia rheumatica
Clinical diagnosis but can also check inflammatory markers: ESR/CRP usually raised Also bloods to exclude differentials: FBC Renal profile (U&E) LFTs Calcium (abnormal in hyperparathyroidism, cancer and osteomalacia) Serum protein electrophoresis for myeloma Thyroid-stimulating hormone for thyroid function Creatine kinase for myositis Rheumatoid factor for rheumatoid arthritis Urine dipstick Anti-nuclear antibodies (ANA) for systemic lupus erythematosus Anti-cyclic citrullinated peptide (anti-CCP) for rheumatoid arthritis Urine Bence Jones protein for myeloma Chest x-ray for lung and mediastinal abnormalities (e.g., lung cancer or lymphoma)
83
Treatment of polymyalgia rehumatica
Reducing regime of prednisolone: 15mg until the symptoms are fully controlled, then 12.5mg for 3 weeks, then 10mg for 4-6 weeks, then Reducing by 1mg every 4-8 weeks
84
What is the additional management for patients on long term steroids? (there is a mnemonic)
Don't STOP: Don’t – steroid dependence occurs after 3 weeks of treatment, and abruptly stopping risks adrenal crisis S – Sick day rules (steroid doses may need to be increased if the patient becomes unwell) T – Treatment card – patients should carry a steroid treatment card to alert others that they are steroid-dependent O – Osteoporosis prevention may be required (e.g., bisphosphonates and calcium and vitamin D) P – Proton pump inhibitors are considered for gastro-protection (e.g., omeprazole)
85
What are the four bony parts of the ankle?
Medial malleolus Lateral malleolus Tibial plafond Talus
86
What are the main symptoms of an ankle fractue
Bony tenderness over the injured area Inability to walk four weight bearing steps immediately after the injury/in A&E Soft tissue swelling Deformity - ankle dislocation Neurovascular deficity - dislocation can cause nerve injury or compression
87
What are the investigations for an ankle fracture
X-ray Full neurovascular assessment: Dorsalis pedis and posterior tibialis pulse Capillary refill in toes Sensation over dorsum of foot, first web spaces, distal sole and heel Ottowa ankle rules
88
What are the Ottowa ankle rules and what are its components?
Determine the need for radiographs in acute ankle injuries An ankle X-ray is only required if: There is any pain in the malleolar zone; and, Any one of the following: Bone tenderness along the distal 6 cm of the posterior edge of the tibia or tip of the medial malleolus, OR Bone tenderness along the distal 6 cm of the posterior edge of the fibula or tip of the lateral malleolus, OR An inability to bear weight both immediately and in the emergency department for four steps.
89
What is Weber classification of the lateral malleolus
Type A - below the ankle joint - syndesmosis intact Type B - at level of ankle joint - syndesmosis intact or partially torn Type C - above the ankle joint - syndesmosis will be disrupted
90
According to the Ottowa rules, when is a foot x-ray indicated?
A foot X-ray series is indicated if: There is any pain in the midfoot zone; and, Any one of the following: Bone tenderness at the base of the fifth metatarsal (for foot injuries), OR Bone tenderness at the navicular bone (for foot injuries), OR An inability to bear weight both immediately and in the emergency department for four steps.
91
Treatment for ankle fractures
Usually open reduction and internal fixation
92
What are the two different locations of hip fractures?
Intracapsular - Femoral head fractures: These are rare and often associated with dislocations. - Femoral neck fractures: More common and further classified as subcapital, transcervical, and basicervical. Extracapsular - Intertrochanteric fractures: Occur between the greater and lesser trochanters. - Subtrochanteric fractures: Occur below the lesser trochanter.
93
What is the system called which grades a hip fracture
Garden system classifications: Type I: Stable fracture with impaction in valgus Type II: Complete fracture but undisplaced Type III: Displaced fracture, usually rotated and angulated, but still has boney contact Type IV: Complete boney disruption Blood supply disruption is most common following Types III and IV.
94
What are the symptoms of a hip fracture
Pain Shortened and externall rotated leg Patients with non-displaced or incomplete neck of femur fractures may be able to weight bear
95
Treatment for hip fractures
Intracapsular: Undisplaced Fracture: internal fixation, or hemiarthroplasty if unfit. Displaced Fracture: Arthroplasty (total hip replacement or hemiarthroplasty) to all patients with a displaced intracapsular hip fracture Total hip replacement is favoured to hemiarthroplasty if patients: - were able to walk independently out of doors with no more than the use of a stick and - are not cognitively impaired and - are medically fit for anaesthesia and the procedure. Extracapsular: Management stable intertrochanteric fractures: dynamic hip screw if reverse oblique, transverse or subtrochanteric fractures: intramedullary device
96
What is the most commonly fractured metatarsal
The proximal 5th metatarsal
97
What are the three different types of metatarsal fractures
Proximal avulsion fractures (pseudo-jones) - occurs at proximal tuberosity and is associated with lateral ankle sprain/inversion injuries Jones fracture - transverse fracture at the metaphyseal-diaphyseal junction Metatarsal stress fracture - occurs in athletes, most common site is 2nd metatarsal shaft
98
What are the symptoms of a metatarsal fracture
Pain and bony tenderness Swelling Antalgic gait
99
Investigations for metatarsal fractures
X-ray - determines whether stable, displaced or stress fracture Stress fractures do not show on x-rays hence: Isotope scan or MRI
100
Whats the difference between direct and indirect injury to the patella
Direct - usually follows a direct blow or trauma to the front of the knee Indirect - happens when the quadriceps forcefully contracts against a block to knee extension
101
Clinical features of a patella fracture
Swelling Bruising Pain and tenderness around the knee Palpable gap may be felt
102
Investigations for a patella fracture
AP and lateral x-rays Skyline vciew if diagnosis is sitll unclear after AP and lateral
103
Management of a patella fracture
Undisplaced (particularly vertical fractures with intact extensor mechanism) - hinged knee brace for 6 weeks and patients allowed to fully weight bear Displaced & loss of extensor mechanism - operative management w/ tension band wire, inter-fragmentary screws or cerclarge wires followed by hinged knee brace for 4-6 weeks
104
What are the risk factors for developing achilles tendon disorders
Quinolone use - ciprofloxacin Hypercholesterolaemia (predisposed to tendon xanthomata)
105
What are the symptoms of achilles tendonopathy (tendonitis)
Gradual onset of posterior heel pain that is worse following activity Morning pain and stiffness
106
Management for achilles tendonopathy (tendonitis)
Supportive Simple analgesia Reduction in precipitating activity Calf muscle eccentric exercises
107
What may a patient describe if they have ruptured their achilles tendon
Audible pop in ankle Sudden nset significant pain in calf or ankle Inability to walk or continue playing sports
108
How to examine if a patient has ruptured their achilles tendon
Simmond's triad: Ask patient to lie prone with feet hanging off the bed 1) Abnormal angle of declination - injured foot may be more dorsiflexed 2) Squeeze the calf muscle and the foot should plantarflex, injured foot will not mvoe 3) Feel for a gap in the tendon
109
Investigation and management for achilles tendon rupture
Ultrasound Refferal to orthopaedics
110
What is a sprain
stretching, partial or complete tear of a ligament
111
What is a syndesmosis
fibrous joint in which two adjacent bones are linked by a strong membrane or ligaments E.G. syndesmosis beween tibia and fibular
112
How do patients with a lower ankle sprain present
Pain Swelling and Tenderness over affected ligament Usually able to weight bear unless severe
113
How do youy classify low ankle sprains
Grade 1 (mild) - stretch or micro tear to ligament, minimal bruising and swelling, no pain on weight bearing Grade 2 (moderate) - Partial tear to ligament, Moderate brusing and swelling and minimal pain on weight bearing Grade 3 (severe) - complete tear to ligament, severe bruising and swelling, severe pain on weight bearing
114
Investigations for a low ankle sprain
X-ray accoridng to Ottowa ankle rules (to check for fracture) MRI - if persistent pain
115
Most common mechanism of injury for high ankle sprains
External rotation of the foot causing talus to push fibula laterally
116
Presentation of high ankle sprains
Pain Swelling Tenderness Pain when squeezing tibia and fibula together (Hopkin's squeeze test)
117
Investigations for high ankle sprains
X-ray - widening of tibiofibular joint (diastasis) or ankle mortise MRI - if suspicious of syndesmosis injury
118
Treatment for high ankle sprains
IF no diastasis - non-weight bearing orthosis or cast until pain subsides IF diastasis (or failed non-operative management) - operative fixation
119
What is iliotibial band syndrome
Most common cause of lateral knee pain in runners
120
What are the symptoms of iliotibial band syndrome
tenderness 2-3cm above the lateral joint line
121
Management of iliotibial band syndrome
Activity modification and iliotibial band stretches IF no improvement then physiotherapy referral
122
Common mechanisms of injry to the anterior cruciate ligament (ACL)
Lateral blow to the knee Sudden twising Akward landing
123
Presentation of an ACL injury
Sudden popping sound Knee swelling Instability - feel as if knee is going to give way
124
Investigations for ACL injury
Anterior draw test Lachman's test
125
Most common mechanism of injury to the meniscus
Twisting force to knee
126
Symtpoms of a meniscal tear
Pain worse on straightening knee Knee may give way May cause knee locking (if displaced) Tenderness along the joint line
127
What investigation can be done to check for meniscal tears
Thessaly's test -weight bearing at 20 degrees of knee flexion Positive if pain on twisting
128
What is Chondromalacia patellae
Softening of the cartilage of the patella most commonly seen in teenage girls
129
Features and treatment of Chondromalacia patellae
Anterior knee pain on walking up and down stairs and rising from prolonged sitting Physiotherapy
130
Features of Osgood-Schlatter disease
Pain Tenderness and Swelling over the tibial tubercle
131
Features of Osteochondritis dissecans
Pain after exercise Intermittent swelling and locking
132
Features of Patellar subluxation
Medial knee pain due to lateral subluxation of the patella Knee may give way
133
Features of Patellar tendonitis
Most commonly seen in athletic teenage boys Chronic anterior knee pain that worsens after running Tender below the patella on examination
134
Symptoms of plantar fasciitis
Heel pain Usually worse around the medial calcaneal tuberosity
135
Management of plantar fasciitis
Rest the feet Wear shoes with good arch support and cushioned heels Insoles and heel pads may be helpful
136
What is a Boxer's fracture and what is the most common cause?
Minimally displaced fracture of the 5th metacarpal Patient punching a hard surface
137
What is a Colle's fracture and what is the most common cause?
Dorsally displaced distal radius fracture (DDDr F) Caused by a fall onto an outstretched hand (FOOSH) AKA dinner fork type deformity
138
What are the early complications of a Colle's fracture
Median nerve injury -acute carpal tunnel syndrome Compartment syndrome , Vascular compromise Malunion Rupture of the extensor pollicis longus tendon
139
What are the late complications of a Colle's fracture?
Osteoarthritis Complex regional pain syndrome
140
What are the the features of a Colle's fracture
Transverse fracture of the radius 1 inch proximal to the radio-carpal joint Dorsal displacement and angulation
141
What is a Smith's fracture and what is the most common cause?
Reverse Colle's fracture Volar angulation of distal radius fragments Caused by falling backwards onto the palm or the flexed wrists
142
What is a Bennett's fracture and what is the most common cause? What is shown on X-rays?
Intra-articular fracture of the first carpometacarpal joint Impact on flexed metacarpal, caused by fist fights X-ray: triangular fragment at ulnar base of metacarpal
143
What is a Monteggia's fracture and what is the most common cause?
Dislocation of the proximal radioulnar joint in association with an ulna fracture Fall on outstretched hand with forced pronation
144
What is a Galeazzi fracture? What is the most common cause?
Radial shaft fracture with associated dislocation of the distal radioulnar joint Direct blow
145
What is a Pott's fracture? What is the most common cause?
Bimalleolar ankle fracture Forced foot eversion
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What is a Barton's fracture? What is the most common cause?
Distal radius fracture (Colles'/Smith's) with associated radiocarpal dislocation Fall onto extended and pronated wrist
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How can humeral fractures be divided?
Proximal humeral fracture Humeral shaft fractures Distal humeral fractures
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What is a supracondylar fracture?
Distal humerus fracture just above the elbow joint
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What are the features of a supracondylar fracture?
Pain Swelling over the elbow immediately Elbow typically in a semi-flexed position
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What is the management of a supracondylar fracture?
Non-displaced - collar and cuff Displaced - manipulation and fixation under anaesthesia
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What are the features of a scaphoid fracture?
Pain along the radial aspect of the wrist and base of thumb Maximum tenderness at the anatomical snuffbox Wrist joint effusions Pain elicited by telescoping of the thumb Pain on ulnar deviation of the wrist Loss of grip/pincer strength
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Causes of a scaphoid fracture
Fall on outstretched hand (FOOSH)
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Investigations for scaphoid fracture
X-ray with PA, lateral and oblique views
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Initial management of scaphoid fracture
Immobilisation with a futuro splint or standard below-elbow back slab
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Orthopaedic management of scaphoid fracture
Undisplaced - cast for 6-8 weeks Displaced - surgical fixation
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Complications of scaphoid fracture
Avascular necrosis
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Features of a radial head fracture and most common cause
Fall on outstretched hand Local tenderness over head of radius Impaired movement at elbow Sharp pain at the lateral side of the elbow at the extremes of rotation (pronation and supination).
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What is De Quervain's tenosynovitis
Sheath containing the extensor pollicis brevis and abductor pollicis longus tendons is inflamed
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Features of De Quervain's tensosynovitis
Pain on radial side of wrist Tenderness over radial styloid process Abduction of thumb against resistance is painful Finkelstein's test - examiner pulls the thumb of the patient in ulnar deviation and longitudinal traction = pain over the radial styloid process and along the length of extensor pollisis brevis and abductor pollicis longus
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Management of De Quervain's tensosynovitis
Analgesia Steroid injection Immobilisation with thumb splint
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What are 5 causes of elbow pain?
Lateral epicondylitis (Tennis elbow) Medial epicondylitis (Golfer's elbow) Radial tunnel syndrome Cubital tunnel syndrome Olecranon bursitis
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Features of lateral epicondylitis
Pain and tenderness localised to lateral epicondyle pain worse on resisted wrist extension with the elbow extended or supination of the forearm with the elbow extended
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Features of medial epicondylitis
pain and tenderness localised to the medial epicondyle pain is aggravated by wrist flexion and pronation
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Features of radial tunnel syndrome and nerve involved
Similar to lateral epicondylitis pain tends to be around 4-5 cm distal to the lateral epicondyle symptoms may be worsened by extending the elbow and pronating the forearm compression of the posterior interosseous branch of the radial nerve.
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Features of cubital tunnel syndrome
Due to ulnar nerve compression Initially intermittent tingling in the 4th and 5th finger May be worse when the elbow is resting on a firm surface or flexed for extended periods Later numbness in the 4th and 5th finger with associated weakness
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Features of olecranon bursitis
Swelling over posterior aspect of elbow Pain Warmth Erythema
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Management of lateral epicondylitis
Advice on avoiding muscle overload Simple analgesia Steroid injection Physiotherapy
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What is a compound fracture
When the skin is broken and the broken bone is exposed to the air. The broken bone can puncture through the skin
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What is a stable fracture
When the fractured bone remains in alignment at the fracture
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What is a pathological fracture
When a bone breaks due to abnormality within bone
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What fractures most commonly occur in children?
Greenstick Buckle Salter-Harris (growth plate fractures)
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What bones are at risk of avascular necrosis if fractured
Scaphoid Femoral head Humeral head Talus Navicular 5th metatarsal
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What diseases can cause pathological fractures
Osteoporosis Tumour Paget's disease of the bone
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What are the main cancers that metastasis to the bone
PoRTaBLe Prostate Renal Thyroid Breast Lung
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What is the FRAX tool
Risk of a fragility fracture over the next 10 years
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What are fragility fractures
Fractures caused by weakness of bone (usually due to osteoporosis)
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How is bone mineral density measured
DEXA scan
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What are the interpretations of the DEXA scan
T-scores More than -1 = Normal -1 to -2.5 = Osteopenia Less than -2.5 = Osteoporosis Less than -2.5 + plus fracture = severe osteoporosis
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First line treatments for reducing the risk of fragility fractures
Calcium and Vitamin D Bisphosphonates (e.g. alendronic acid)
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Side effects of bisphosphonates
Reflux and oesophageal erosions Atypical fractures Osteonecrosis of the jaw Osteonecrosis of the external auditory canal
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What is an alternative to bisphosphate in fragility fractures prophylaxis
Denosumab - blocks activity of osteoclasts
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When can a fat embolism occur
Following the fracture of long bones May become lodged in vessels - PE
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Management of fat embolism
Operating early to fix the fracture reduces the risk of fat embolism syndrome
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What is reactive arthritis
Synovitis in one or more joints following an infective trigger
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What are the common triggers of reactive arthritis
Gastroenteritis STIs
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What organisms are most commonly associated with reactive arthritis
Chlamydia trochamatis Shigella flexneri Salmonella Yersinia enterocolitica Campylobacter
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What are the symptoms of reactive arthritis
Typically develops within 4 weeks of initial infection - symptoms last around 4-6 months Asymmetrical oligoarthritis of lower limbs Warm, swollen and painful joint Dactylitis Anterior uveitis Bilateral conjunctivitis Urethritis Circinate balanitis (dermatitis to head of penis) "Cant see, pee or climb a tree"
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Management of reactive arthritis
Symptomatic NSAIDs Intra-articular steroids Persistent disease: sulfasalazine and methotrexate
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What is rheumatoid arthritis
Autoimmune condition causing chronic inflammation in the synovial lining of joints, tendon sheaths and bursa
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What is the disease pattern of rheumatoid arthritis
Symmetrical (distal - hands and feet) polyarthritis
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Risk factors for rheumatoid arthritis
Obesity Smoking HLADR4 Family history
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Presentation of rheumatoid arthritis
Swollen painful joints in the hands and feet Stiffness worse in the morning Gradually gets worse with larger joints becoming involved Positive 'squeeze test' Fatigue Weight loss flu like symptoms
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What are the most commonly affected joints in rheumatoid arthritis
MCP joints PIP joints Wrist MTP joints
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What is palindromic rheumatism and what are its symptoms
Self limiting episodes of inflammatory arthritis Pain, stiffness and swelling typically affecting a few joints
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What can indicate that palindromic rheumatism may develop into rheumatoid arthritis
Positive rheumatoid factor and anti-CCP
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What are the joint signs in rheumatoid arthritis
Z-shaped deformity of the thumb Swan neck deformity (hyperextended PIP and flexed DIP) Boutonniere deformity (hyperextended DIP and flexed PIP) Ulnar deviation Atlantoaxial subluxation - can cause spinal cord compression
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What are the extra-articular manifestations of rheumatoid arthritis
Pulmonary fibrosis Bronchiolitis obliterans Cardiovascular disease Sjogren's syndrome Felty's syndrome (triad of rheumatoid arthritis, neutropenia and splenomegaly) Anaemia of chronic disease Caplan syndrome (pulmonary nodules in patients with RA exposed to asbestos, silica and coal) Lymphadenopathy
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What are the ocular manifestations of rheumatoid arthritis
Keratoconjunctivitis sicca Episcleritis Scleritis Keratitis Cataracts (secondary to steroids) Retinopathy (secondary to hydroxychloroquine)
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What are the investigations of rheumatoid arthritis
Rheumatoid factor Anti-CCP antibodies CRP and ESR X-ray of hands and feet Ultrasound or MRI if clinical findings are unclear
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What are the X-ray changes in rheumatoid arthritis
LESS Loss of joint space Erosions Soft-tissue swelling See-through bones (osteopenia)
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What scoring system measures functional ability in rheumatoid arthritis
Health Assessment questionnaire (HAQ)
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What scoring systems monitors disease activity in rheumatoid arthritis
Disease Activity Score 28 Joints (DAS28) Assigns points for: Swollen joints Tender joints ESR/CRP results
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What is the management of rheumatoid arthritis
DMARD monotherapy +/- short course of bridging prednisolone Methotrexate Leflunomide Sulfasalazine Hydroxychloroquine If not successful with monotherapy then combination treatment with multiple DMARDs If still not successful then biological therapies (usually alongside methotrexate) - TNF inhibitors - adalimumab, infliximab and etanercept - Anti-CD20 on B cells - rituximab
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How are flares of rheumatoid arthritis managed
Oral or IM corticosteroids
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How should methotrexate be taken
Once a week Since it interferes with folic acid metabolism: + folic acid 5mg (on a different day)
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Side effects of methotrexate
Mouth ulcers and mucositis Liver toxicity Bone marrow suppression and leukopenia Teratogenic
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Side effects of leflunomide
Hypertension Peripheral neuropathy Mouth ulcers and mucositis Liver toxicity Bone marrow suppression and leukopenia Teratogenic
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Side effects of sulfasalazine
Orange urine Reversible male infertility Bone marrow suppression
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Side effects of hydroxychloroquine
Retinal toxicity - reduces visual acuity Blue-grey skin pigmentation Hair lightening (bleaching)
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Side effects of rituximab
Night sweats and thrombocytopenia
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What medications can cause reactivation of tuberculosis
Anti-TNF medications: adalimumab, infliximab and etanercept
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What rheumatoid arthritis drug is teratogenic
methotrexate
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What are the poor prognostic features fir rheumatoid arthritis
RF positive Anti-CCP antibodies Poor functional status at presentation HLADR4 X-ray: early erosions (e.g. after <2 years) Insidious onset
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What are the most common causative agents in septic arthritis
Staphylococcus aureus Neisseria gonorrhoea - in young adults that are sexually active then Group A strep - streptococcus pyogenes Haemophilus influenza E.coli
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What is the presentation of septic arthritis
Acutely hot, red, swollen, painful joint Stiffness and reduced range of motion Fever Lethargy Sepsis
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Differential diagnoses of septic arthritis
Pseudogout Gout Reactive arthritis Hemarthrosis
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Investigations for septic arthritis
Synovial fluid sampling via joint aspiration - shows leucocytosis - gram staining is negative in around 30-50% of cases - fluid culture is positive in patients with non-gonococcal septic arthritis Blood cultures Joint imaging
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Management of septic arthritis
IV Flucloxacillin (clindamycin if allergic) for 4-6 weeks Switches to oral after 2 weeks Needle aspiration to decompress joint Arthroscopic lavage may be required
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What are the seronegative spondyloarthropathies
Ankylosing spondylitis Psoriatic arthritis Reactive arthritis Enteropathic arthritis
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After how long does psoriatic arthritis develop after having psoriasis?
Usually within in 10 years
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What are the 5 patterns of psoriatic arthritis
Asymmetrical oligoarthritis - affects 1-4 joints of the body on one side Symmetrical polyarthritis (similar to rheumatoid arthritis) - more than four joints affected (usually hands, wrists and ankles) Distal interphalangeal joint disease - primarily only affects the DIP joints Spondylitis - presents with back stiffness and pain (involves axial skeleton - spine and sacroiliac joints) Arthritis mutilans (most severe form of psoriatic arthritis) - osteolysis of the phalanges around the joints leading to shorter digits resulting in skin folds (telescoping digit)
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What is a good way of distinguishing between rheumatoid arthritis and psoriatic arthritis
PA usually affects the DIP joints whereas RA does not
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What are the features of psoriatic arthritis
Psoriatic skin lesions Enthesitis Dactylitis Nail pitting Onycholysis Uveitis IBD
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What is the tool used for screening for psoriatic arthritis in patients with psoriasis
Psoriasis Epidemiological Screening Tool (PEST) Involves questions about joint pain, swelling, history of arthritis and nail pitting
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Investigations for psoriatic arthritis
X-ray: Periostitis - inflammation of periosteum around bone = thickening and irregular outline of bone Ankylosis - fusion of bones at the joint Osteolysis - destruction of bone Dactylitis - Inflammation of the whole digit - soft tissue swelling PENCIL IN CUP appearance - associated with arthritis mutilans
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What is the management of psoriatic arthritis
Mild peripheral arthritis/axial disease = NSAIDs Moderate/severe = DMARDs - methotrexate, leflunomide, sulfasalzine Can also use: Ustekinumab and secukinumab (monoclonal antibodies) Anti-TNF - etanercept, infliximab, adalimumab Apremilast (phosphodiesterase type-4 (PDE4) inhibitors
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What is SLE
Systemic inflammatory autoimmune connective tissue disorder
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In who does SLE most commonly occur in
Women Asian, African, Caribbean and Hispanic Young to middle-aged adults
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What is the disease pattern of SLE
Relapsing-remitting
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What are the symptoms of SLE
General: Fatigue Fever Mouth ulcers Lymphadenopathy Skin: Malar rash Discoid rash - scaly, erythematous, well demarcated rash ins un exposed areas Photosensitivity Raynaud's phenomenon MSK: Arthralgia Non-erosive arthritis Cardiovascular: Pericarditis Myocarditis Respiratory: Fibrosing alveolitis Pleurisy Renal: Proteinuria Glomerulonephritis Neuropsychiatric: Anxiety and depression Psychosis Seizures
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Investigations for SLE
Anti-nuclear antibodies (ANA) - 99% positive (high sensitivity but low specificity) Anti-dsDNA - highly specific RF - 20% are positive ESR and CRP may be raised in active inflammation Complement (C3 and C4) levels are low Urinalysis - urine protein:creatinine ratio shows proteinuria
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What can occur secondary to SLE
antiphospholipid antibodies and antiphospholipid syndrome
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Management for SLE
NSAIDs Sun block Hydroxychloroquine IF internal organ involvement then consider: prednisolone cyclophosphamide More severe SLE DMARDs - methotrexate Rituximab Belimumab
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What are the complications of SLE
Cardiovascular: Hypertension Anaemia Pericarditis Pleuritis Pulmonary fibrosis Lupus nephritis Optic neuritis Transverse myelitis Recurrent miscarriage VTE
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What are sarcomas
Cancers originating in the muscles, bones or connective tissues
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What are three types of bone sarcomas
Osteosarcoma - most common form of bone cancer Chondrosarcoma - originating from cartilage Ewing sarcoma - bone and soft tissue cancer affecting children/young adults
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What are the different soft tissue sarcomas
Rhabdomyosarcoma - of skeletal tissue Leiomyosarcoma - of smooth muscle Liposarcoma - of adipose tissue Synovial sarcoma - of soft tissues surrounding joints Angiosarcoma - of blood and lymph vessels
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What are the key features of sarcomas
A soft tissue lump, particularly if growing, painful or large Bone swelling Persistent bone pain
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Investigations for sarcomas
X-ray - for bony lumps or persistent bone pain US - if soft tissue lump CT/MRI - used to look for metastatic spread Biopsy - histology of cancer
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Treatments for sarcomas
Surgery - resection Radiotherapy Chemotherapy Palliative care
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What are the most common sites to be affected in osteosarcoma
Femur Tibia Humerus
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Presentation of osteosarcoma
Seen mainly in children and adolescents Persistent bone pain Worse at night and may disturb/wake them up from sleep Bone swelling Palpable mass Restricted joint movement
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Investigations for osteosarcoma
Urgent X-ray within 48 hours, shows: Poorly defined lesion in bone Destruction of normal bone Fluffy appearance of bone Irritation of lining of bone = 'sunburst' appearance Bloods: raised ALP Staging scans: MRI, CT, Bone scan, PET scan, Biopsy
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Management of osteosarcoma
Surgical resection of the lesion with limb amputation Adjuvant chemotherapy
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What is an osteoma and where does it typically occur
Overgrowth of bone Commonly occurs in the skull
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What is an osteochondroma
Most common benign bone tumour Cartilage-capped bony projection on external surface of bone
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What is a giant cell tumour and how is it shown on an x-ray
Tumour of multinucleated giant cells withing a fibrous stroma Occurs most commonly in the epiphyses of long bones X-ray shows soap bubble appearance
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Where do chondrosarcomas most commonly occur
Axial skeleton
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Where do Ewing's sarcoma most commonly occur and what is shown on x-ray
Pelvis and long bones Tends to cause severe pain X-ray shows 'onion skin' appearance
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Other than bone pain, what are the common features of bone cancer
pathological fractures Hypercalcaemia Raised ALP
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What are the most common sites for bone metastases
Spine Pelvis Ribs Skull Long bones
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What symptoms are suggestive of spinal metastases
Unrelenting lumbar back pain Any thoracic or cervical back pain Worse with sneezing, coughing, or straining Nocturnal Associated with tenderness
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What investigation should be done in anyone with suspected spinal metastases
MRI
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What is the Mirel's scoring system
A classification system that evaluates the risk of a pathologic fracture in a lesion
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What are the causes of mechanical back pain
Muscle or ligament sprain Facet joint dysfunction Sacroiliac joint dysfunction Herniated disk Spondylolisthesis (anterior displacement of a vertebra out of line with the one below) Scoliosis Degenerative changes to discs and facet joints (arthritis)
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What are the causes of neck pain
Muscle or ligament sprain Torticollis (waking up with a unilaterally stiff and painful neck due to muscle spasm) Whiplash (typically after a road traffic accident) Cervical spondylosis
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What are the red flag causes of back pain
Spinal fracture Cauda equina Spinal stenosis (e.g., intermittent neurogenic claudication) Ankylosing spondylitis Spinal infection
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What spinal nerves join o form the sciatic nerve?
L4 - S3
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What nerves branch off the sciatic nerve once it reaches the knee?
Tibial nerve Common peroneal nerve
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What are the causes of sciatica
Herniated disc Spondylolisthesis Spinal stenosis
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Symptoms of sciatica
Unilateral pain from buttocks radiating down back of thigh to below knee or feet Paraesthesia Numbness Motor weakness
263
What is the sciatic stretch test
Helps diagnose sciatica The patient lies on their back with their leg straight. The examiner lifts one leg from the ankle with the knee extended until the limit of hip flexion is reached (usually around 80-90 degrees). Then the examiner dorsiflexes the patient’s ankle. Sciatica-type pain in the buttock/posterior thigh indicates sciatic nerve root irritation. Symptoms improve with flexing the knee.
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What investigations can be done for lower back pain
Usually a clinical diagnosis X-rays and CT scans MRI - emergency for cauda equina Inflammatory markers
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What is the STarT Back Screening Tool
Stratifies the risk of a patient presenting with acute back pain developing chronic back pain.
266
How to manage non-specific lower back pain
IF low risk of developing chronic back pain: Self management Education Reassurance Analgesia - NSAIDs first line, Codeine alternative, Benzodiazepines (diazepam) for muscle spasms (short term only) Stay active IF medium or high risk: Physiotherapy Group exercise CBT SAFETY NET FOR RED FLAGS - CAUDA EQUINA SYMPTOMS
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Management of sciatica
Initial management is same as lower back pain management For analgesia use: Amitriptyline Duloxetine Chronic options: Epidural corticosteroid injections Local anaesthetic injections Radiofrequency denervation Spinal decompression
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What is spinal stenosis
Narrowing of the spinal canal leading to compression of the spinal cord or nerve roots
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What are the three types of spinal stenosis
Central stenosis - narrowing of the central spinal canal Lateral stenosis - narrowing of the nerve root canals Foramina stenosis - narrowing of the intervertebral foramina
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What are the causes of spinal stenosis
Congenital spinal stenosis Degenerative changes (including facet joint changes, disc disease and bone spurs) Herniated discs Thickening of the ligamental flava or posterior longitudinal ligament Spinal fractures Spondylolisthesis Tumours
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Presentation of spinal stenosis
Intermittent neurogenic claudication (lumbar spinal stenosis with central stenosis), symptoms include: Lower back pain Buttock and leg pain Leg weakness Symptoms absent at rest and sitting but arise when walking or standing after sitting Bending expands spinal canal therefore relieves symptoms (vice versa for standing)
272
How to differentiate intermittent neurogenic claudication and PAD?
Take ABPI - normal in spinal stenosis Spinal stenosis patients have back pain, PAD does not
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Investigations for spinal stenosis
MRI ABPI and CT angiogram to rule out PAD
274
Management of spinal stenosis
Exercise and weight loss Analgesia Physiotherapy Decompression surgery (if all else fails) - laminectomy (removal of part of lamina from vertebra)
275
Examples of large vessel vasculitis
GCA - temporal arteritis Takayasu's arteritis
276
Examples of medium vessel arteritis
Polyarteritis nodosa Kawasaki disease
277
Examples of small vessel vasculitis
ANCA-associated vasculitis: Granulomatosis with polyangiitis Eosinophilic granulomatosis with polyangiitis Microscopic polyangiitis Immune complex small-vessel vasculitis: Henoch-Schoenlein purpura Goodpasture's syndrome (anti-glomerular basement membrane disease)
278
Which vasculitides are p-ANCA and c-ANCA positive?
p-ANCA: Microscopic polyangiitis Eosinophilic granulomatosis with polyangiitis c-ANCA: Granulomatosis with polyangiitis
279
What is Henoch-Schoenlein purpura
IgA vasculitis IgA deposits in the blood vessels
280
Symptoms of Henoch-Schoenlein purpura
Purpura Joint pain Abdominal pain Renal involvement (IgA nephritis) - raised creatinine, haematuria and proteinuria
281
Management of Henoch-Schoenlein purpura
Supportive: Analgesia Rest Hydration If using steroids, monitor with: Urine dipstick - to check for renal involvement BP - to monitor hypertension
282
Features of microscopic polyangiitis
Renal failure due to glomerulonephritis Diffuse alveolar haemorrhage - haemoptysis
283
Features of granulomatosis with polyangiitis
Most commonly affects respiratory tract and kidneys: Nose: Epistaxis Crusting around nose Nasal secretions Saddle shaped nose Ears: Hearing loss Sinuses: Sinusitis Lungs: Cough Wheeze Haemoptysis Kidneys: Glomerulonephritis
284
Eosinophilic granulomatosis with polyangiitis
Most commonly affects lungs and skin Severe asthma Sinusitis Allergic rhinitis
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Characteristic finding on FBC in eosinophilic granulomatosis with polyangiitis
Raised eosinophils
286
What infection can polyarteritis nodosa be secondary to
Hepatitis B
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Features of polyarteritis nodosa
Renal impairment Hypertension Tender, erythematous skin nodules MI Stroke Mesenteric arteritis - GI symptoms
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Features of Kawasaki's disease
CRASH and BURN Conjunctivitis (Bilateral) Rash (widespread erythematous maculopapular rash) Adenopathy Strawberry tongue Hands and feet swelling (desquamation) and Persistently high fever for more than 5 days
289
What vessel does Takayasu's arteritis most commonly affect
Aorta and its branches + pulmonary arteries
290
Features of Takayasu's arteritis
Fever Malaise Muscle aches Claudication symptoms in the upper limb Stenosis or occlusion can reduce pulses and BP in a limb = 'pulseless disease)
291
Investigations for Takayasu's arteritis
CT or MRI angiography: vessels can swell and form aneurysms or become narrowed and blocked
292
What are the general features of vascultidies
Joint and muscle pain Peripheral neuropathy Renal impairment Purpura GI symptoms Necrotic skin ulcers + SYSTEMIC SYMPTOMS: Fatigue Fever Night sweats Anorexia Weight loss Anaemia
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Investigations for vasculitis
Inflammatory markers - ESR and CRP p-ANCA c-ANCA Urinalysis for haematuria and proteinuria
294
General management of vasculitis
Steroids: oral prednisolone IV hyrdrocortisone Nasal for nasal symptoms Inhaled for lung involvement immunosuppressants: Cyclophaosphamide Rituximab
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