RHEUM Flashcards
Blood results consistent with polymyalgia rheumatica?
CRP + ESR = high
CK + anti-CCP = normal
Antibodies associated with limited cutaneous systemic sclerosis?
anti-centromere
Antibodies associated with diffuse cutaneous systemic sclerosis?
Anti-Scl-70
Antibodies associated with drug induced lupus?
Anti-histone antibodies
What happens to APTT in antiphospholipid syndrome?
Prolonged APTT
Spinal XR findings in ankylosing spondylitis?
Squaring of lumbar vertebrae
Subchondral erosions
Sclerosis
Management of acute flares of rheumatoid arthritis?
PO prednisolone OR IM methylprednisolone
Early XR findings in rheumatoid arthritis?
Loss of joint space
Juxta-articular osteoporosis
Soft tissue swellings
Late XR findings in rheumatoid arthritis?
Periarticular erosions
Subluxation
What is the only non-inflammatory arthritis?
OA.
List 3 seropositive causes of arthritis.
RA SLE Scleroderma Vasculitis' Sjogren's syndrome
List 3 seronegative causes of arthritis.
Psoriatic arthritis
Reactive arthritis
Enteric arthritis
Ankylosing spondylitis.
List the main cause of infective arthritis.
Septic arthritis.
List the 2 types of crystal induced arthritis.
Gout
Pseudogout
What is meant by the term ‘spondyloarthropathies’?
A group of related chronic inflammatory conditions that tend to affect the axial skeleton and have certain shared clinical features.
Name 3 of the spondyloarthropathies.
Ankylosing spondylitis
Psoriatic arthritis
Enteric arthritis
Reactive arthritis
Name 3 features that spondyloarthropathies tend to have in common.
1) Seronegative
2) HLA27 positive
3) Axial arthritis (spine + sacroiliac joints)
4) Enthesitis (inflammation at tendon/ ligament insertion sites.
5) Dactylitis (inflammation of an entire digit)
List 3 of the extra-articular joint manifestations which can be associated with spondyloarthropathies.
Iritis Oral ulcers Psoriaform rashes IBD Aortic valce incompetence
In which patients are extra-articular manifestations of rheumatoid arthritis more likely?
In those with high titres of RF and anti-CCP as these create abnormal IgG, citrullinated type 2 collagen + vimentin.
Lung manifestations of RA?
Pulmonary fibrosis/ bronchiolitis obliterans
Skin manifestations of RA?
Rheumatoid nodules
Cardiac manifestations of RA?
CVD
IHD
Pericarditis
Pericardial effusion
Eye manifestations of RA?
Scleritis
Episcleritis
Cataracts 2o to steroid treatment
MSK manifestations of RA?
Carpal tunnel syndrome
Tendon ruptures
Frozen shoulder
De Quervain’s tenosynovitis
What is Felty’s syndrome?
RA + neutropenia + splenomegaly.
What is Sicca syndrome?
secondary sjogren’s syndrome.
What is Caplan’s syndrome?
RA + pulmonary fibrosis + pulmonary nodules.
What is anti-phospholipid syndrome?
A disorder associated with anti-phospholipid antibodies where the blood becomes prone to clotting, causing a hypercoaguable state.
Anticardiolipin antibodies?
Antiphospholipid syndrome.
Anti-beta-2 glycoprotein I antibodies?
Antiphospholipid syndrome
What is systemic sclerosis?
An autoimmune inflammatory and fibrotic connective tissue disorder.
What are the 2 types of systemic sclerosis?
Limited cutaneous
Diffuse cutaneous
Features of limited cutaneous systemic sclerosis?
CREST syndrome:
Calcinosis Raynaud's phenomenon Oesophageal dysmotility Sclerodactyly Telangiectasia
Features of diffuse cutaneous systemic sclerosis?
Features of CREST syndrome PLUS effects on internal organs:
HTN CAD Pulmonary HTN Pulmonary fibrosis Glomerulonephritis
What is Sjogren’s syndrome?
An autoimmune condition affecting exocrine glands + leading to symptoms of dry mucous membranes (eyes, mouth, vagina).
What is primary Sjogren’s syndrome?
Occurs in isolation.
What is secondary Sjogren’s syndrome?
Occurs secondary to another disease (SLE or RA).
Anti-Ro + Anti-La antibodies?
Sjogren’s syndrome.
Special test for Sjogren’s syndrome?
Schirmer test (if <10mm = significant).
What is polymyositis?
Chronic inflammation of the muscles.
What is dermatomyositis?
Chronic inflammation of the skin + muscles.
Diagnostic investigation for polymyositis/ dermatomyositis?
CK (often >1000).
Anti-Jo-1 antibodies?
Polymyositis (sometimes dermatomyositis).
Anti-Mi-2 antibodies?
Dermatomyositis
Dermatomyositis antibodies?
Anti-Mi-2
ANA
What is vasculitis?
Inflammatory disorders for the blood vessels characterised based upon the size of the blood vessels that they affect.
List 3 small vessel vasculitis’.
Henoch-Schonlein Purpura
Eosinophilic granulomatosis with polyangiitis
Microscopic polyangiitis
Granulomatosis with polyangiitis
List 3 medium vessel vasculitis’.
Polyarteritis nodosa.
Eosinophilic granulomatosis with polyangiitis.
Kawasaki disease.
List 2 large vessel vasculitis’.
GCA
Takayasu’s arteritis.
ESR + CRP in vasculitis.
Elevated.
pANCA associated vasculitis’?
Microscopic polyangiitis.
Eosinophilic polyangiitis with granulomatosis.
cANCA associated vasculitis’?
Granulomatosis with polyangiitis.
What is Marfan’s syndrome?
Autosomal dominant connective tissue disorder.
Where is the defect in Marfan’s syndrome?
On the gene coding for fibrillar 1.
Renal failure ± SOB ± haemoptysis?
Microscopic polyangiitis.
Enteric arthritis is associated with what conditions?
IBD
GI bypass surgery
Coeliac disease.
When does enteric arthritis usually improve?
Upon treatment of the underlying bowel disease.
What can be used for resistant cases of enteric arthritis?
DMARDs.
Define osteoarthritis.
Non-inflammatory arthritis described as ‘wear and tear’ within synovial joints.
Most common aetiology of OA.
Genetic factors + overuse + injury.
3 causes of secondary OA.
Joint disease Obesity Occupation Injury Haemochromatosis
5 risk factors for development of OA.
Increasing age Obesity Female sex Certain occupations Trauma/ injury Exercise stresses Joint misalignment Joint laxity
Joints most common affected by OA.
Hips, knees, small joints of hands.
5 general features of OA?
1) Joint pain + stiffness worsened by activity.
2) Deformity, swelling + reduced function/ ROM.
3) Asymmetrical distribution across joints.
4) Gelling of joints after rest.
5) Background ache in joint at rest.
6) Instability.
7) Warmth + tenderness if synovitis.
8) Pain ± crepitus on movement.
Which parts of the hands are commonly affected by OA?
Carpals
DIPJs
PIPJs
Thumb MCP joint
**NOTE: other MCPs are not involved.
Signs of OA on the hands?
1) Squaring at base of thumb.
2) Bouchard’s nodes at PIPJs.
3) Heberden’s nodes at DIPJs.
4) Mucoid cysts adjacent to joint on dorsal surface (can cause nail ridging).
**Potential wasting of thenar muscles.
How is OA pain in the hands typically exacerbated?
Pinching/ strong grip actions.
Where will the pain be in OA of the hip?
Deep pain in anterior groin on walking/ climbing stairs.
Where is pain referred to in OA of the hip?
Lateral thigh + buttock
Anterior thigh + knee.
Movement most affected by OA of the hip?
Internal rotation with hip flexion.
Features of advanced OA in the hip?
Trendelenberg gait.
Fixed flexion external rotation deformity.
What would suggest patellofemoral involvement in OA of the knee?
Pain worse on walking upstairs and even more so on walking downstairs.
When can diagnosis of OA be clinical?
If patient is >45, has typical activity related pain + no morning stiffness is present.
Bedside investigations for OA?
History
Examination
Weight + BMI
Blood investigations for OA?
CRP can be slightly elevated.
Imaging investigations for OA?
Plain XR if diagnostic uncertainty/ to exclude other diagnoses.
Signs of OA seen on XR?
Loss of joint space Osteophyte formation Subarticular sclerosis (increased density of bone along joint line) Subchondral cysts (fluid filled holes in bone)