MSK joint disorders Flashcards
comprises a heterogeneous group of
arthritides of unknown cause beginning in
children up to 18 years of age (most
commonly begins during the toddler or early
adolescent period) and occurring for at least
6 weeks.
JIA
JIA Pain is often ____ and less severe,
but presents in the morning and early during
the day rather than the more common
presentation of growing pains at night.
dull and achy
The most common type of JIA (accounting for half of all JIA cases)
Pauciarticular(oligoarticular) JIA
Generally affects four or fewer joints during the first 6 months of
disease
Pauciarticular JIA
Does pauciarticular JIA have symmetric or asymmetric pattern?
asymmetric
What joints does Pauciarticular mostly effect
knees, elbows, wrists, and ankles.
in pauciarticular boys are more affected between ages 1-5 true or false
girls
Affects five or more joints, most commonly including large and small joints.
Polyarticular JIA
Joint involvement is usually symmetric/asymmetric and is most like that of adult RA, with
the potential for severe, destructive arthropathy.
symmetric
Polyarticular JIA affects girls or boys more
girls
Rheumatoid factor–positive (RF+)
The presence of rheumatoid factor.
Subcutaneous nodules, cervical spine fusion, chronic uveitis, and destructive hip disease.
part of rheumatoid factor positive
Theumatoid factor–negative (RF-)
Children with this subtype do not test positive for rheumatoid factor.
Joint involvement usually less severe.
Morning stiffness and fatigue with possible low-grade fever are common.
Involvement of any number of joints.
Systemic-onset JIA (Still Disease)
Often begins with a high-spiking fever and chills that appear
intermittently for weeks and may be accompanied by a rash on the
thighs and chest that often goes away within a few hours.
Systemic-onset JIA (Still Disease)
The child may also experience macrophage activation syndrome and
lymphadenopathy; inflammation of the liver, spleen, heart, and
surrounding tissues; and anemia.
Systemic-onset JIA (Still Disease)
A group of disorders formerly considered variants of RA, are in fact
distinct entities with similar features affecting the spine.
Spondyloarthropathies (SpAs)
A group of disorders formerly considered variants of RA, are in fact
distinct entities with similar features affecting the spine.
Spondyloarthropathies (SpAs)
o Ankylosing Spondylitis (AS)
o Sjögren syndrome
o Psoriatic arthritis
o Reactive arthritis including arthritides that accompany inflammatory
bowel disease (known as enteric arthritides)
o Reiter syndrome.
Spondyloarthropathies (SpAs)
Common Features of the
Spondyloarthropathies
Chronic inflammation of the axial skeleton and sacroiliac joints.
Asymmetric involvement of a small number of peripheral joints.
Young males (late teens, early adulthood) most affected.
Familial predisposition.
Inflammation at sites of ligament, tendon, and fascial insertion into
bone.
Seronegativity for rheumatoid factor, but an association with
histocompatibility antigens including HLA-B27.
Extraarticular involvement of eyes, skin, genitourinary tract, cardiac
system.
An inflammatory arthropathy of the axial
skeleton including the sacroiliac joints,
apophyseal joints, costovertebral joints, and
intervertebral disk articulations.
Ankylosing Spondylitis
(Marie-Strümpell disease)
does AS have symmetric or asymmetric involvement?
asymmetric
What age does AS usually affect?
Typically affects young people, beginning between the ages of 15 and
30 years (rarely after age 40 years).
When is back pain occur?
This differs from back pain of mechanical origin, which is much
more likely to develop 30-65