Rheumatology 3 Flashcards

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)

A

HTN

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
Q

Name the rotator cuff muscles and function

A

Supraspinatus abducts arm before deltoid
Infraspinatus rotates arm laterally
Teres minor adducts and rotates arm laterally
Subscapularis adducts and rotates arm medially

26
Q

Sjorgren’s serology (3)

A

Anti Ro La
ANA 70%
RhF 50%

27
Q

What is Sjojren’s?
Primary and secondary
Gender
Increased risk of?

A

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
Q

Features Sjogren’s (6)

A

Dry eyes - keratoconjunctivitis sicca
Dry mouth
Vaginal dryness
Arthralgia
Raynauds
Recurrent episodes of parotitis

29
Q

Sjogren’s Mx (2)

A

Artificial saliva and tears
Pilocarpine

30
Q

Sulfasalazine pregnancy and breastfeeding?

A

Safe in pregnancy and breastfeeding

31
Q

SLE
Gender
Ethnicity

A

F>M
Afro-Carribean

32
Q

Features SLE (5)

A

Malar rash
Discoid rash - scaly, well demarcated rash in sun exposed areas
Photosensitivity
Livedo reticularis
Raynauds

33
Q

SLE serology (3)

A

ANA
anti-dsDNA specific
anti-Smith

34
Q

Monitoring in SLE (3)

A

ESR
Low C2, C4 during active disease
anti-dsDNA

35
Q

What is systemic sclerosis?
Classification
Gender

A

Hardened, sclerotic skin
F>M

Limited - face and distal limbs

Diffuse - trunk and proximal limbs

36
Q

Limited systemic sclerosis
First sign
Which areas?
Antibodies
Extra

A

Raynauds
Distal limbs and face
Anti-centromere
CREST - calcinosis, Raynauds, oesophageal dysmotility, sclerodactyly, telangiectasia

36
Q

What is CREST?
Which disease is it a subtype of?

A

Limited systemic sclerosis
CREST - calcinosis, Raynauds, oesophageal dysmotility, sclerodactyly, telangiectasia

37
Q

Systemic sclerosis antibodies
General
Limited
Diffuse

A

ANA 90%
anti-centromere limited
Scl 70 diffuse

38
Q

What is scleroderma?

A

Tightening of the skin without internal organ involvement

39
Q

Diffuse systemic sclerosis
Location
Antibodies
Most common cause of death
Organ involvement
Prognosis

A

Trunk and proximal limbs
Scl 70
ILD and pulmonary arterial hypertension
Renal and HTN
Poor

40
Q

Osteoporosis mx
Steroids >65
Steroids <65
Fragility fracture >75
Fragility fracture <75
Women >65
Men >75
>40yo with RF
<40yo RF

A
  • 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