Rheum Flashcards
IgA nephropathy (Berger’s diseae) with systemic vasculitic involvement =
IgA vasculitis (Henoch-Schonlein Purpura)
Features of IgA Vasculitis (Henoch-Schonlein Purpura)
Purpura on extensors/buttocks
Abdo pain (GI bleeding)
Nephritis
(Polyarthritis)
IgA vasculitis (HSP) usually presents in
Children following an infection
anti-scl-70 (anti-topoisomerase) is highly specific for:
Diffuse cutaneous systemic sclerosis (+ increased risk pulmonary fibrosis)
anti-centromere is highly specific for:
Limited cutaneous systemic sclerosis
anti-dsDNA is highly specific for:
SLE
anti-Smith is highly specific for:
SLE
anti-Mi-2 is highly specific for:
Dermatomyositis
but only present in 25%
anti-Jo-1 is seen in
Polymyositis (in disease with lung involvement, Raynauds & fever)
Indications for plasma exchange (plasmapharesis)
Guillain-Barre
Myasthenia gravis
Goodpastures
ANCA vasculitis with rapidly progressive GN
ANCA vasculitis with pulmonary haemorrhage
TTP/HUS
Cryoglobulinaemia
Hyperviscosity (eg in MM)
Anti-Ro are seen in
Sjogrens
Also SLE
SLE and pregnant - Which antibody signifies risk of neonatal heart block
Anti-Ro
Initial management of RA
DMARD monotherapy (usually methotrexate)
+/- bridging steroids
Other DMARD options in RA
Sulfasalazine
Leflunomide
Hydroxychloroquine
Management of RA - inadequate response to DMARDs
at least 2 DMARDs, including MTX
TNF-inhibitors:
Etanercept
Infliximab
Adalimumab
Before starting TNF-inhibitor
Screen for TB, Hep B
(+/-Hep C if risk) due to risk of re-activation
Abatacept (anti-CTLA4) used in
RA not controlled with anti-TNF therapy
Canakinumab (anti-IL1) used in
Gout flares
Resistant Still’s disease
Management of RA - next step after TNF inhibition
Rituximab (anti-CD20)
Tocilizumab (anti-IL6) used in
RA not controlled with anti-TNF therapy
Management of dermatitis herpetiformis
GF diet
Topical dapsone
Side effect of dapsone
Haemolytic anaemia
Peripheral neuropathy
Management of scalp psoriasis
Potent topical corticosteroid (Beclomethasone)
Features of Adult Onset Still’s Disease
Daily fevers
Salmon-pink rash
Oligoarthritis
Serositis
Management of Still’s disease
NSAIDs -> Steroids -> MTX -> anti-TNF -> anti-IL1 (canakinumab) -> anti-IL6 (Tocilizumab)/anti-CD20 (rituximab)
1st line therapy for plaque psoriasis
Topical steroids / Vit D analogues / Dithranol / Coal tar
2nd line therapy for plaque psoriasis
UVB light therapy
Ciclosporin/MTX
3rd line therapy for plaque psoriasis (or with arthritis)
anti-TNF (infliximab)
Aspirate findings in pseudogout
Positively birefringent rhomboid crystals
Aspirate findings in gout
Negatively birefringent needle-shaped crystals
Management of pseudogout
NSAIDs > Steroids > Colchicine
Management of gout
NSAIDS/colchicine -> Oral steroids -> IM steroid
Alemtuzumab (anti-CD52) is used in
Multiple sclerosis
Commonest causes of drug-induced lupus
Hydralazine
Procainamide
Isoniazid
Phenytoin
Typical antibodies in drug-induced lupus
anti-dsDNA negative
anti-histone positive
Features of thromboangiitis obliterans
Young men, smokers Peripheral limb ischaemia Cockscrew vessels Lack of CVD RF Lack of multisystem inflammation
Features of antiphospholipid syndrome
VTE Thrombocytopenia Prolonged APTT Livedo reticularis Recurrent fetal loss Pre-eclampsia, pulmonary HTN
Management of antiphospholipid syndrome (no previous VTE)
Low-dose aspirin
Management of antiphospholipid syndrome (previous VTE)
Lifelong warfarin with INR target 2-3
Management of antiphospholipid syndrome (recurrent VTE whilst on warfarin)
Lifelong warfarin INR 3-4
Add aspirin
Management of antiphospholipid syndrome (previous arterial thrombosis)
Lifelong warfarin INR 2-3