juvenile idiopathic arthritis Flashcards
JIA
condition affecting children and adolescents where autoimmune inflammation occurs in the joints.
arthritis without any other cause (pain, limited range of motion, tenderness, warmth), lasting more than 6 weeks in a patient under the age of 16
features of JIA
joint pain, swelling and stiffness.
types of JIA
Systemic JIA
Polyarticular JIA
Pauciarticular JIA
Enthesitis related arthritis
Juvenile psoriatic arthritis
some people prefer enjoying joints
systemic JIA aka stills disease
Subtle salmon-pink rash. trunk and thighs
High swinging fevers, rise to 39.5 daily for 2 weeks
Enlarged lymph nodes
Weight loss
Joint inflammation and pain
Splenomegaly
Muscle pain
bendy and hyperflexible
Pleuritis and pericarditis
investigations systemic JIA
Antinuclear antibodies and rheumatoid factors typically negative.
raised inflammatory markers, with raised CRP, ESR, platelets and serum ferritin.
polyarticular jia
idiopathic inflammatory arthritis in 5 joints or more
2nd most common
symmetrical
Systemic symptoms are mild
equivalent of rheumatoid arthritis in adults
seronegative usually but can be RF positive
Oligoarticular JIA- pauciarticular
4 joints or less. Usually it only affects a single joint
most common
tends to affect the larger joints
3 types
enthesitis related arthritis
more common in male children over 6 years
paediatric version of the seronegative spondyloarthropathy
MRI scan of the affected joint can demonstrate enthesitis, but cannot distinguish between an enthesitis due to stress or an autoimmune process.
HLA B27 gene positive
consider signs and symptoms of psoriasis and inflammatory bowel disease
anterior uveitis
tender to localised palpation of the entheses
juvenile psoriatric arthritis
psoriasis
joint involvement pattern varies
nail pitting
oncholysis- separation of the nail from the nail bed
dactylitis
enthesitis
management of JIA
1st NSAIDs or steroid injections
2nd methotrexate
anti TNF
IL1R antagonist
IL6 antagonist
systemic steroids in systemic JIA, serious complications, bridge between DMARDs, if undergoing surgery
physio and OT
avoid surgery as much as possible
pauciarticular type1
limp rather than pain
no constitutional manifestations
mainly lower limb
hip very rare
knee most common
positive ANA in 40-75%
50% asymptomatic
uveitis
pauciarticualr arthritis type 2
boys more than girls
limp, mainly lower limb
rare systemic
hip can be affected early with rapid damage
require THR early in life and may progress into spondyloarthritis
HLA B27 and back involvement - ankylosing spondylitis
pauciarticular arthritis type 3
systemic rare
asymmetric UL and LL arthritis
dactylitis
psoriasis in 40%
can be destructive
needs eye screening
polyarticular RF negative
girls much more common any age
low grade fever, malaise
mild anaemia
growth abnormalities
hepato-splenomegaly
symmetrical
uveitis rare
polyarticular RF positive
girls age 12-17
similar to adult RA
erosions in xray occur early
uveitis rare