Rheumatology 3 Flashcards

(41 cards)

1
Q

Pseudogout
What type of crystals
Age

A

Calcium pyrophosphate crystals
>60

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2
Q

Pseudogout RF (5)

A

Haemochromatosis
Hyperparathyroidism
Mag and phos low
Acromegaly
Wilson’s disease

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3
Q

Pseudogout joint aspiration findings

A

Positively birefringent rhomboid shaped crystals

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4
Q

Pseudogout joints affected
XR finding
Mx (3)

A

Knee, shoulders, wrist
XR chrondocalcinosis
Mx NSAIDs, IM/intra-articular/ PO steroids

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5
Q

Psoriatic arthropathy signs (5)
Skin (1)
Feet (3)
Nails (1)

A

Psoriatic plaques
Achilles tendonitis
Plantar fascitis
Dactylitis
Onycholysis + pitting of the nails

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6
Q

XR typical sign psoriasis

A

Pencil in cup appearance

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7
Q

Mx psoriatic arthropathy (3)

A

Secondary care
1. NSAIDs +/- DMARDs
2. Monoclonal antibodies

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8
Q

Raynauds
Age and gender
Unilat or bilat

A

Young women e.g 30yo
Bilateral

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9
Q

Secondary causes of Raynaud’s (6)

A

Scleroderma
ReaA
SLE
Leukaemia
OCP
Cervical rib

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10
Q

Mx Raynaud

A

Secondary care referral
1. Calcium channel blocker e.g nifedipine
2. IV prostacyclin

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11
Q

Reactive arthritis HLA
Classic triad
Onset
How long do symptoms last?
Another symptom

A

HLA B27
Conjunctivitis, urethritis, arthritis
Symptoms develop within 4 weeks post an infection
6 months
Dactylitis - inflammation of a digit

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12
Q

Skin condition associated with reactive arthritis (2)

A

Circinate balanitis (painless vesicles on the head of the penis)
Keratoderma blenorrhagica (waxy yellow/brown papules on palms and soles)

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13
Q

What is Felty’s syndrome?

A

RA + splenomegaly + low white cell count

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14
Q

Classification criteria for RA (4)
Score needed

A

6/10
Joint involvement, serology (RhF or anti-CCP), acute phase reactants (CRP or ESR), duration of sx >6/52

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15
Q

MTX SE (3)

A

Myelosuppression
Pneumonitis
Liver cirrhosis

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16
Q

Sulfasalazine SE (4)

A

Heinz body anaemia/ myelosuppresion
ILD
Oligospermia
Rash - Steven Johnson syndrome
Can stain tears/ contact lenses

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17
Q

Leflunomide SE (1)

18
Q

Hydroxychloroquine SE (2)

A

Retinopathy
Corneal deposits

19
Q

Penicillinamine SE (1)

A

Exacerbation of myasthenia gravis

20
Q

Etanercept SE (2)

A

Demyelination
Reactivation of TB

21
Q

RA Mx long term
Acute
Monitoring response to treatment (2)

A

Long term
1. DMARD (MTX) +/- bridging pred

Acute pred

DAS28/ CRP

22
Q

Examples of DMARDs (4)

A

MTX
Sulfasalazine
Leflunomide
Hydroxychloroquine

23
Q

2nd line treatment of RA
Examples (3)

A

If no response to x2 DMARDs
TNF inhibitors
Etanercept, infliximab, adalimumab

24
Q

RA XR (5)

A

Loss of joint space
Juxta-articular osteoporosis
Soft tissue swelling
Periarticular erosions
Subluxation

25
Name the rotator cuff muscles and function
Supraspinatus abducts arm before deltoid Infraspinatus rotates arm laterally Teres minor adducts and rotates arm laterally Subscapularis adducts and rotates arm medially
26
Sjorgren's serology (3)
Anti Ro La ANA 70% RhF 50%
27
What is Sjojren's? Primary and secondary Gender Increased risk of?
Autoimmune disorder affecting exocrine glands - resulting in dry mucosal surfaces Secondary to RA where it develops 10 years after initial onset F>M Lymphoid malignancy
28
Features Sjogren's (6)
Dry eyes - keratoconjunctivitis sicca Dry mouth Vaginal dryness Arthralgia Raynauds Recurrent episodes of parotitis
29
Sjogren's Mx (2)
Artificial saliva and tears Pilocarpine
30
Sulfasalazine pregnancy and breastfeeding?
Safe in pregnancy and breastfeeding
31
SLE Gender Ethnicity
F>M Afro-Carribean
32
Features SLE (5)
Malar rash Discoid rash - scaly, well demarcated rash in sun exposed areas Photosensitivity Livedo reticularis Raynauds
33
SLE serology (3)
ANA anti-dsDNA specific anti-Smith
34
Monitoring in SLE (3)
ESR Low C2, C4 during active disease anti-dsDNA
35
What is systemic sclerosis? Classification Gender
Hardened, sclerotic skin F>M Limited - face and distal limbs Diffuse - trunk and proximal limbs
36
Limited systemic sclerosis First sign Which areas? Antibodies Extra
Raynauds Distal limbs and face Anti-centromere CREST - calcinosis, Raynauds, oesophageal dysmotility, sclerodactyly, telangiectasia
36
What is CREST? Which disease is it a subtype of?
Limited systemic sclerosis CREST - calcinosis, Raynauds, oesophageal dysmotility, sclerodactyly, telangiectasia
37
Systemic sclerosis antibodies General Limited Diffuse
ANA 90% anti-centromere limited Scl 70 diffuse
38
What is scleroderma?
Tightening of the skin without internal organ involvement
39
Diffuse systemic sclerosis Location Antibodies Most common cause of death Organ involvement Prognosis
Trunk and proximal limbs Scl 70 ILD and pulmonary arterial hypertension Renal and HTN Poor
40
Osteoporosis mx Steroids >65 Steroids <65 Fragility fracture >75 Fragility fracture <75 Women >65 Men >75 >40yo with RF <40yo RF
- On steroids over 65 - treat - On steroids under 65 - DEXA - Fragility fracture + over 75 - treat - Fragility fracture + under 75 - DEXA - Frax assessment for: a) all women over 65, b) men over 75, c) >40yo with risk factors - Younger patients under 40 with major risk factors - DEXA