Rheumatology Flashcards

1
Q

what is the presentation of JIA?

A
joint swelling for at least 6 weeks 
morning stiffness / gelling 
rash
fever
fatigue 
poor appetite 
weight loss 
irritability or refusal to walk in toddlers 
school absence or limited ability to participate in physical activity 
delayed puberty, growth restriction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are differential diagnoses JIA?

A
septic arthritis 
osteomyelitis 
transient synovitis 
recurrent haemarthoses 
vascular abnormalities 
trauma 
malignancies i.e. lymphoma, bone tumour
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are differentiating features of septic arthritis and JIA?

A
JIA affects > 1 joint 
septic arthritis only 1 joint 
septic arthritis joint is swollen hot and red 
JIA isn't red or hot
JIA hx for weeks 
septic arthritis acute hx
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are the features of systemic JIA?

A
arthritis 
intermittent fever > 2 weeks
salmon pink erythematous rash 
generalised lymphadenopathy 
sensitise 
hepatosplenomegaly 
high ESR (normal CRP)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the treatments for JIA?

A

intra-articular steroids
DMARD’s i.e. methotrexate
biologics i.e. Anti TNF alpha

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what type of JIA has poor response to intra articular steroids?

A

oligoarticular JIA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are the complications of uveitis?

A

glaucoma
cataracts
blindness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are the symptoms of uveitis?

A

really symptomatic
redness
headache
reduced vision

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is the treatment for uveitis in JIA?

A

topical steroids (systemic if more severe)

DMARD and biologics if poor response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are some of the signs on clinical examination of a child with JIA?

A
periarticular soft tissue oedema
intra-articular effusion 
tenosynovitis 
pain 
joint held in position of maximum conforrt
range of movement limited at extremities
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what features are required for a diagnosis of psoriatic JIA?

A

chronic arthritis and definite psoriasis + 2 of the following;

dactylics
nail pitting or onycholysis
psoriasis in 1st degree relative
HLA B27 positive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what features are required for a diagnosis of enthesitis-related JIA?

A

at least 2 of the following;

onset of poly arthritis/oligoarthritis in a boy > 8 yrs

sacroiliac joint tenderness

inflammatory spinal pain

acute anterior uveitis

HLA B27 positivity

family history in 1st degree relative

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

in what age of onset and gender is oligoarticular JIA most common?

A

early childhood onset most common in girls 1-5yrs

if late onset most common in boys > 8 yrs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what’s the difference in the distribution of oligoarticular JIA depending on early and late onset?

A

early onset affects hands, knees, ankles and feet

late onset hip involvement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

will children with early onset JIA test positive for ANA?

A

yes - late onset are negative

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

will children with late onset JIA test positive for JANA?

A

no - early onset are positive

17
Q

what are the main differences between early and late onset oligoarticular JIA?

A

early onset

  • girls 1-5 yrs
  • no hip involvement
  • positive ANA
  • uveitis

late onset

  • boys > 8yrs
  • hip involvement
  • no systemic involvement
18
Q

what are the main differences between pauciarticular and polyarticular JIA?

A

pauciarticular/oligoarticular;

  • 4 or less joints
  • asymmetrical
  • large joints

polyarticular;

  • 5 or more joints
  • few or no systemic manifestations
19
Q

is RF positive polyarticular JIA more common in young children or older?

A

older children > 8yrs

20
Q

is RF negative polyarticular JIA more common in younger or older children?

A

younger children < 5yrs

21
Q

what are possible systemic manifestations in polyarticular JIA?

A

hepatosplenomegaly
lymphadenopathy
pericarditis
chronic uveitis

22
Q

what are the complications of JIA?

A

poor growth
localised growth disturbance - leg length discrepency
micrognathia
contractures
ocular complications (due to chronic uveitis)