Rheumatology Flashcards

1
Q

Monoarthritis

A

SA, gout, CPPD, OA, trauma (haemarthrosis)

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2
Q

Polyarthritis

A

Symmetrical - RA, OA, viruses (hep ABC, mumps) systemic conditions
Asymmetrical - reactive, psosriatic

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3
Q

Heberdens nodes

Bouchards nodes

A

B proximal

H distal

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4
Q

Felty’s syndrome

A

RA + splenomegaly + neutropenia

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5
Q

DMARDS, tx RA

A

a combination of
methotrexate (pneumonitis (get urgent respiratory help), oral ulcers,hepatotoxicity)
sulfasalazine (rash, sperm count, oral ulcers) hydroxychloroquine (irreversible
retinopathy (request annual ophthalmology review))

Then biological agents - SE - Serious infection, including reactivation of TB (screen and consider prophylaxis) and hep B; worsening HF etc

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6
Q

Ankylosing Spondylitis

A

HLA B27 +ve

progressive loss of spinal movement (all
directions)—hence reduced thoracic expansion.
kyphosis, neck hyperextension
(question-mark posture)
spino-cranial ankylosis.
enthesitis- esp Achilles tendonitis, plantar fasciitis,
at the tibial and ischial tuberosities, and at the iliac crests.
Anterior mechanical chest pain due to costochondritis and fatigue may feature
Acute iritis occurs in~⅓ of patients and may lead to blindness if untreated
osteoporosis (up to 60%)
aortic valve incompetence (<3%)
pulmonary apical fibrosis.

Sacroiliitis is the earliest X-ray feature

Tx - exercise, NSAIDs, bisphosphonates, TNFa blockers

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7
Q

Spondylarthritidies

A

AS
Enteric arthropathy - IBD, coeliac, GI bypass, Whipples – improves w tx of bowel
Psoriatic Arthritis - symmetrical, NSAIDS,
sulfasalazine, methotrexate and ciclosporin
Reactive arthritis - sterile, affects lower limbs 1-4 weeks after urethritis/ dysentery,

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8
Q

Autoimmune connective tissue diseases

A
systemic sclerosis
primary Sjögren’s
syndrome , idiopathic inflammatory myopathies (myositis), 
mixed connective tissue disease
relapsing polychondritis
Behçet’s disease
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9
Q

Systemic sclerosis

A

Scleroderma/vascular disease
Two types:
Limited cutaneous
Diffuse cutaneous

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10
Q

Polymyositis Tests
Screening
Treatment

A

Muscle enzymes (ALT, AST, LDH, CK & aldolase) in plasma
EMG - fibrillation potentials
**muscle biopsy
MRI muscle oedema in acute
anti-Mi2, anti-Jo1—associated with a syndrome
of acute onset and interstitial lung fibrosis that should be treated aggressively.

SCREEN MALIGNANCY
Steroids
Immunosuppressives

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11
Q

Dermatomyositis

A

Macular rash (shawl sign)
Lilac-purple (heliotrope) rash on eyelids often
with oedema
Nailfold erythema (dilated capillary loops)
Gottron’s papules: Roughened red papules over the knuckles, also seen on elbows and knees
(pathognomonic if CK high + muscle weakness);
Subcutaneous calcifications

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12
Q

Anti-La, anti Ro

A

Sjögren’s

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13
Q

Anti-Smith

A

SLE

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14
Q

Anti Jo-1; Anti-Mi-2

A

Polymyositis, dermatomyositis.

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15
Q

Anti-Scl70

A

Diffuse systemic sclerosis.

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16
Q

Antimitochondrial Ab

A

Primary biliary cirrhosis (>95%), autoimmune hepatitis

30%), idiopathic cirrhosis (25–30%

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17
Q

Anti-smooth muscle Ab (SMA)

A
Autoimmune hepatitis (70%), primary biliary cirrhosis
(50%), idiopathic cirrhosis (25–30%)
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18
Q

Coeliac disease ab

A

a gliadin Ab, antitissue transglutaminase, anti-endomysial Ab

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19
Q

C ANCA

A

Granulomatosis + polyangiitis

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20
Q

Perinuclear (p-ANCA), MPO +ve

A

Microscopic polyangiitis

(45%), Churg–Strauss,

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21
Q

Anti-voltage-gated Ca2+-channel Ab:

A

Lambert Eaton Syndrome

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22
Q

Anti-aquaporin 4:

A

Devic’s disease - neuromyelitis optica

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23
Q

Anti-double-stranded DNA

24
Q

Antihistone Ab

A

drug induced SLE

25
Anticentromere ab
Limited SS
26
ANA
SLE, autoimmune hep, sjogrens
27
SLE- Pathology
autoantibodies are made against a variety of autoantigens polyclonal B-cell secretion of pathogenic auto anti bodies causing tissue damage > immune complexes, complement activation
28
SLE-Diagnosis
``` Malar Rash Photosensitivity Discoid Rash Renal - proteinuria CNS disorders Serositis -Pleura/ pericarditis Arthritis - non erosive Oral ulcers Haem -Low counts - anaemia (haemolytic) Ab prescence ANA +ve ```
29
SLE treatment
IV cyclophosphamide + high-dose prednisolone | maintence - NSAIDs, hydroxychloroquine, steroids
30
APLS
Coagulation defect, Livedo reticularis, Obstetric (recurrent miscarriage), Thrombocytopenia Tx - low dose aspirin
31
Vasculitis Large
Giant cell arteritis, Takayasu’s arteritis
32
Medium Vasculitis
Polyarteritis nodosa, Kawasaki disease
33
Small Vasculitis
ANCA +ve -predilection for respiratory tract and kidneys. p-ANCA associated microscopic polyangiitis, lomerulonephritis and Churg–Strauss syndrome and c-ANCA associated Wegener’s granulomatosis ANCA –ve -HSP, goodpasture’s syndrome, cryoglobulinaemia.
34
Polymyalgia rheumatica
CRP high, ESR typically >40 (but may be normal); ALP is high in 30%. Note CK levels are normal (helping to distinguish from myositis/myopathies Prednisolone
35
Pseudogout patho
deposition of calcium pyrophosphate dihydrate crystals in the synovium.
36
Pseudogout XR findings
chondrocalcinosis
37
Pseudogout aspiration
joint aspiration: weakly-positively birefringent rhomboid-shaped crystals
38
Pseudogout RF
``` haemochromatosis hyperparathyroidism acromegaly low magnesium, low phosphate Wilson's disease ```
39
What is gout?
deposition of monosodium urate monohydrate in the synovium
40
Risk factors for gout
thiazides, drugs, alcohol, poor eGFR, red meat, CVD, myeloproliferative disorders, cytotoxic drugs, psoriasis, Lesch Nyhan syndrome
41
What to do on gout follow up
Check urate, BP, CVD risks Council re ULT Advance px
42
Acute mx of gout
``` colchicine - diarrhoea NSAIDS high dose - 2 days post sx Pred 15mg Steroid injections Cont allopurinol ```
43
Aim of urate lowering therapy
<300
44
SLE antibodies
``` Anti ANA (sens, not spec) Anti Smith (specific) Anti DsDNA ```
45
APLS findings
CLOT - coagulation, livedo reticularis, obs issues, | Prolonged APTT
46
APLS management
Lifelong aspirin If VTE/ arterial clot - lifelong warfarin. Target 2-3 If clot on warfarin - 3-4
47
APLS management in pregnancy
Low dose aspirin | Then LMWH once fetal heartbeat > 34 weeks.
48
Raynauds management
``` Nifedipine IV prostacyclin (epoprostenol) infusions: effects may last several weeks/months ```
49
Large vessel vasculitis
GCA, Takayasus arteritis
50
Medium vessel vasculitis
Polyarteritis nodosa, Kawasakis
51
Small vessel vasculitis
P anca - microscopic polyangitis | C anca - wegeners
52
Takayasus arteritis
``` Aorta Woman, asian absent limb pulse, different BPs Systemic sx - malaise, headache Steroids ```
53
Polyarteritis Nodosa
Men medium sized vessels, necrotising inflammation > aneurysms Ass w Hep B
54
Diffuse cutaneous systemic sclerosis
``` whole body organ fibrosis - all Antitopoisomerase-1 antibodies (Anti-Scl70) - 40% Anti RNA polymerase 20% Control BP, annual ECHO, spiro ``` Tx - IV cyclophosphamide BP ACE - prevent renal crisis
55
Limited cutaneous Systemic Sclerosis
``` Calcinosis, Raynauds, Eesophageal/ gut dysmotility, Sclerodacytly, Telangectasia Hands, feet, face Pulmonary HTN Anti centromere - 80% Tx - sildenafil, bosentan (pulm HTN) ```
56
Behcets Disease
Classic triad: oral ulcers genital ulcers anterior uveitis HLA B51