Rheumatology/immunology Flashcards

1
Q

Wegener’s granulomatosis
- AKA
- What is it?
- Classic triad
- Where else?

A

Granulomatosis with polyangiitis

Small and medium vessel vasculitis

Classic triad = URT, LRT, pauci-immune glomerulonephritis.

Also cutaneous, ocular, PNS, MSK

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2
Q

Churg-Strauss syndrome
- AKA
- Classic triad
- blood count feature

A

Eosinophilic granulomatosis with polyangiitis

classic triad = asthma, gastrointestinal and cardiac involvement.

significant (>10% of WBC) peripheral eosinophils or tissue eosinophilia

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3
Q

Goodpasture’s syndrome
- AKA
- Where

A

Anti-glomerular basement membrane antibody disease

Pulmonary haemorrhage and glomerulonephritis. Not at other sites

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4
Q

Berger’s disease/IgA nephropathy

A

Commonest GN in adults worldwide.

Nephritic syndrome 24-48hr post URTI

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5
Q

Post-streptococccal glomerulonephritis

A

Visible haematuria 1-3 weeks after onset of streptococcal infection

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6
Q

Henoch-Schönlein Purpura
- AKA
- demographic
- systemic features

A

IgA vasculitis

Predominantly occurs in children

Systemic features = purpuric rash, abdominal pain, joint pain, GI bleeding

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7
Q

Myasthenia gravis diagnosis

A

Electromyography under repetitive stimulation - will see progressive decrease in amplitude of muscle potential

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8
Q

Peanut/penicillin anaphylaxis immune mediator

A

IgE on presensitised basophils and mast cells

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9
Q

Selective IgA deficiency

A

Absent IgA - needed for mucous membrane infections
May develop anti-IgA antibodies so risk of anaphylaxis with blood transfusions or IVIG

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10
Q

C1 inhibitor deficiency AKA
Cause/mechanism
Presentation
Management

A

Hereditary angio-edema

Unchecked activation of classic complement pathway

Cutaneous angio-oedema, abdominal pain, airway obstruction

Acute: FFP (contains C1-INH)
Prophylaxis: androgens, TXA

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11
Q

Behcet’s disease
- describe
- features
- management

A

Chronic multisystem vasculitis

Oral/genital ulcers, arthritis, iritis, neurological disease

Corticosteroids, anti-TNFa

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12
Q

Rhuematoid factor what kind of Immunoglobulin?

A

IgM

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13
Q

Immunoglobulin in secretions (tears, saliva, sweat)

A

IgA

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14
Q

Rheumatoid arthritis
- management

A

Methotrexate, sulfasalazine

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