Rheumatology Flashcards
(80 cards)
Hi there π«΅ Ψ³Ω ΩΩΩ Ψ§ΩΩΩ
Ψ¨Ψ³Ω Ψ§ΩΩΩ Ψ§ΩΨ±ΨΩ Ω Ψ§ΩΨ±ΨΩΩ π‘
What is Juvenile Idiopathic Arthritis (JIA) βοΈ
π§ Chronic arthritis in children <16 years old , lasting β₯6 weeks
β οΈ Diagnosis of exclusion
## footnote
π Must rule out: infection, malignancy, trauma, systemic diseases, post-infectious causes
What are the main subtypes of JIA and their criteria βοΈ
πΈ Oligoarticular JIA : β€4 joints
πΈ Polyarticular JIA : β₯5 joints
πΈ Systemic-onset JIA :
ββ’ High spiking fever β₯2 weeks
ββ’ Salmon-pink rash , arthritis
ββ’ Hepatosplenomegaly, serositis
What are the typical joint symptoms of JIA βοΈ
𦴠Painful, tender, warm, swollen joints
β° Worse in the morning
πΆ Limping often seen
## footnote
β οΈ Symptoms persist β₯6 weeks
What systemic symptoms are seen in systemic-onset JIA βοΈ
π₯ Daily fever spikes
π΄ Salmon-colored, non-pruritic rash
𧬠Serositis: pleuritis, pericarditis, ascites
π« Hepatosplenomegaly
How is JIA diagnosed βοΈ
π§ͺ Clinical diagnosis β no definitive test
β οΈ Must rule out:
ββ’ Infection, SLE, leukemia, reactive arthritis
ββ’ HSP, osteomyelitis, sarcoidosis
π§ͺ RF, ESR, CRP may help classify but are not diagnostic
What is the importance of uveitis screening in JIA βοΈ
π Uveitis = inflammation of uveal tract
β οΈ Risk highest in oligo/polyarticular JIA <7 years with positive ANA
What is the recommended frequency of eye screening for uveitis in JIA βοΈ
π
Systemic JIA: Every 12 months
π
Oligo/Poly JIA >7 yrs OR ANA-negative: Every 6 months
π
Oligo/Poly JIA <7 yrs & ANA-positive: Every 3β4 months
What is the treatment approach for mild JIA βοΈ
π NSAIDs
π Intra-articular corticosteroid injections
What is the treatment for systemic-onset JIA βοΈ
π Oral/IV corticosteroids
𧬠Biologics (e.g., anakinra , IL-1 inhibitors)
π§ Add methotrexate as a disease-modifying agent
What are the key clinical features of juvenile psoriatic arthritis βοΈ
𦴠Arthritis in small and large joints
πΏ Psoriatic skin rash (if present)
β
If rash is absent β‘οΈ Look for:
ββ’ Family history of psoriasis
ββ’ Nail pitting
ββ’ Dactylitis (βsausage digitβ)
What are the recommended screening and labs in juvenile psoriatic arthritis βοΈ
ποΈ Uveitis risk β‘οΈ Screen with slit-lamp exam every 6 months
π§ͺ Lab tests:
ββ’ ANA
ββ’ HLA-B27
What is Enthesitis-Related Arthritis (ERA) and who is typically affected βοΈ
π§ A subtype of JIA seen in older children >8 years
𦴠Associated with pain, stiffness, and limited mobility of the lower back
π Commonly involves sacroiliac joints and lower extremity arthritis
What lab marker is commonly positive in Enthesitis-Related Arthritis βοΈ
π§ͺ HLA-B27 positive
π§ Strong genetic association, similar to adult spondyloarthropathies
A 15-year-old develops monoarthritis a week after Streptococcus group G pharyngitis. What is the most probable diagnosis βοΈ
β
Post-streptococcal reactive arthritis (PSRA)
## footnote
π§ Clues:
β’ Group G strep (not group A β excludes ARF)
β’ No migratory pattern , no major Jones criteria
β’ Incomplete response to NSAIDs
β’ Monoarthritis in a teenager
β‘οΈ PSRA is a non-rheumatic post-infectious arthritis
What is the recommended treatment for post-streptococcal reactive arthritis βοΈ
π NSAIDs (often insufficient alone)
π Short course of steroids may be needed
## footnote
π« No clear indication for long-term prophylaxis like ARF
What are the clinical features of septic arthritis in children βοΈ
π¨ Ill-appearing child
π₯ High-grade fever >38.5Β°C
π CRP : elevated
π©Έ WBC : >12,000 cells/mL
β Unable to bear weight
β Refuses to move joint
π©» Pain with extreme rotation
## footnote
π Rx: Antibiotics + surgical drainage
What are the clinical features of transient synovitis in children βοΈ
π Well-appearing child
π‘οΈ Mild or no fever
π CRP: normal or slightly raised
π©Έ WBC: normal or slightly elevated
β
Able to bear weight
𦴠Restricted abduction
π¦ Often follows recent URTI
π Rx: Analgesics + bed rest (self-limiting)
What is the most distinguishing clinical difference between septic arthritis and transient synovitis βοΈ
π§ Septic arthritis : child is toxic, febrile, cannot bear weight
π§ Transient synovitis : child is well, afebrile or mildly febrile, can bear weight
What are the key clinical features of Systemic Lupus Erythematosus (SLE) βοΈ
π» Photosensitivity
π» Painless oral ulcers
π» Malar rash (butterfly-shaped)
π» Non-erosive arthritis
π» Serositis (pleuritis or pericarditis)
π» Renal disorder (persistent proteinuria)
π» Neurologic disorder (e.g., seizures)
π» Hematologic disorder (anemia, leukopenia, lymphopenia)
Which autoantibodies are important in the diagnosis of SLE βοΈ
π§ͺ Anti-dsDNA β diagnostic & used to monitor disease activity
π§ͺ Anti-Smith (Sm) β highly specific
π§ͺ ANA β very sensitive (positive in ~99% of SLE cases)
What complement levels are associated with SLE disease activity βοΈ
π C3 and C4 are low or undetectable during active disease
## footnote
π§ Useful for monitoring disease flares
How is SLE managed in children βοΈ
π Hydroxychloroquine (first-line for skin/joint symptoms)
π Corticosteroids for flares
π Cyclophosphamide or other immunosuppressants for severe organ involvement
π NSAIDs for arthritis
β Supportive:
ββ’ Monitor BP & renal function
ββ’ Calcium + Vitamin D
ββ’ No live vaccines if immunosuppressed
ββ’ School accommodations, diet, and vitamin support
Which antibody is most specific for diagnosing SLE βοΈ
A. ANA
B. Anti-dsDNA
C. Rheumatoid factor
D. Anti-Smith antibody
π
D. Anti-Smith antibody
## footnote
Anti-Smith (Sm) antibody is highly specific for SLE, although not always present.