Disease profiles Flashcards

1
Q

Who tends to present with ankylosing spondylitis?

A

Men more than women
Presents age 20-30

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2
Q

What is the clinical presentation of ankylosing spondylitis?

A

Morning joint or back stiffness
Back or buttock pain that improves with activity
Back or joint pain at night which prompts waking
May have systemic features eg heart and eyes
‘Question mark’ posture
Positive Schober’s test

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3
Q

What is the management of ankylosing spondylitis?

A

Conservative:
- Physio
- Exercise
NSAIDs
Corticosteroids
Other analgaesia
Consider biologics
Consider surgery

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4
Q

Who tends to present with gout?

A

Men more than women
In women, usually post- or peri-menopausal
More common in Asians

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5
Q

What are the risk factors for gout?

A

Genetic susceptibility
Overproduction or underexcretion of urate
Being male
Rich diet eg red meats, seafood, alcohol,
Associated with diabetes, heart disease and metabolic syndrome

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6
Q

What is the clinical presentation of gout?

A

Acutely inflamed, hot, swollen joint that reached peak pain within 6-12 hours of onset
Most commonly affects the first MTP joint but may also affect knee
Gouty tophi

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7
Q

What are the investigations and their results for gout?

A

Synovial fluid aspiration - shows negatively birefringent crystals with polarised light
Blood tests may show elevated urate
X-rays may show periarticular punched-out erosions

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8
Q

What is the management of gout?

A

Maintain a healthy weight
Reduce red meat and seafood in diet
Restrict alcohol intake
NSAIDs
Colchicine
Consider steroids

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9
Q

Who is typically affected by OA?

A

Older people

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10
Q

What is the clinical presentation of OA?

A

Joint pain, swelling and stiffness that lasts less than 30 mins in a morning
Hip OA pain may be referred as knee pain or antero-medial groin pain
Pain worse with activity and better with rest
May have bony abnormalities eg Heberden’s and Bouchard’s nodes

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11
Q

Which joints are most commonly affected in OA?

A

Knees, hips, PIPs, DIPs and carpometacarpal joint of thumb

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12
Q

What is the difference between Heberden’s and Bouchard’s nodes?

A

Bouchard’s nodes affect the PIPs and Heberden’s nodes affect the DIPs

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13
Q

What are the features of OA on x-ray?

A

Loss of joint space
Osteophytes
Subchondral cysts
Subchondral sclerosis

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14
Q

What is the management of OA?

A

Physio
Analgaesia
Consider surgery

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15
Q

Which HLA is associated with rheumatoid arthritis?

A

HLA-DR

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16
Q

Which HLA is associated with reactive arthritis, psoriatic arthritis, AS and inflammatory bowel disease?

A

HLA-B27

17
Q

What are the risk factors for sarcoidosis?

A

Afro-caribbean or scandinavian descent

18
Q

What is the clinical presentation of sarcoidosis?

A

Age 20-40
Flu like illness
May be pyrexial
Pulmonary symptoms most common
Dry cough
Dyspnoea
Cutaneous changes eg erythema nodosum and maculopapular rash
Associated with lyme disease
Dry eyes
Anterior uveitis
Hypercalcaemia features

19
Q

What are the investigations if sarcoidosis is suspected?

A

CXR
Blood tests
Spirometry
Tuberculin skin test (should be negative in sarcoidosis)

20
Q

What is the treatment of sarcoidosis?

A

Observe if early
Later stages - oral or inhaled corticosteroids
Consider topical corticosteroids

21
Q

What are the risk factors for osteomalacia?

A

Vit D deficiency
Disorders of phosphate wasting
Type 2 renal tubular acidosis
Excessive use of mineralisation inhibitors (biphosphonates)

22
Q

What are the clinical features of osteomalacia?

A

Bone pain and tenderness (especially in long bones or pelvis)
Muscle weakness (usually proximal)
Fractures with little or no trauma
Poor mobility and impaird gait
Signs of hypocalcaemia
May be asymptomatic

23
Q

What are the investigations if osteomalacia is suspected?

A

Calcium - reduced or normal
Phosphate - reduced or normal
Alk phos - raised
Serum 250HD - reduced
U&Es
PTH - reduced
X ray - diffuse demineralisation, pseudofractures, coarsened traberculae, insufficiency fractures