Rheumatology Flashcards
Recurrent episodes of periodic fevers every 3-5 days, serositis (peritonitis, less commonly pleuritis/pericarditis), joint pains, and erysipelas-like rash; family history of disorder. What is the patient’s likely ethnicity? Most likely complication of disorder?
Familial Mediterranean Fever
Mediterranean
Amyloidosis due to increase Acute Phase reactants during attacks.
True or false. Complex regional pain syndrome can be preceded by a traumatic trigger and lead to somatic changes in involved extremity (mottling, cool to touch, demineralization of bone).
True, requires multidisciplinary approach (PT/OT).
True or false. Kingella kingae is the most common cause of septic arthritis in kids <4 years of age.
False. Staph aureus is the most common cause in ANY age group of septic arthritis. K. kingae is more commonly seen in <4 years old, would add CTX to Vanc/clinda if suspect that.
Antibody(ies) most specific for SLE?
Anti-Smith, Anti-dsDNA
Antibodies for neonatal lupus?
Anti-Ro (SS-A) and Anti-La (SS-B) antibodies
Drug induced lupus antibodies?
Anti-histone antibodies
Most frequent cause of congenital heart block?
Neonatal Lupus, may also have associated cardiac structural anomalies (transposition and septal defects)
Lab abnormalities for SLE?
Anemia, thrombocytopenia, leukopenia, elevated transaminases
Factors that indicate worse prognosis in SLE?
Renal and neurological manifestations
Mixed Connective Tissue Disease antibody?
anti-U1 RNP
Calcium deposits in the muscle/skin can be seen in which rheumatologic condition?
Dermatomyositis
Anti-citrullinated protein antibodies are useful in the diagnosis of which condition?
Rheumatoid arthritis
Systemic JIA
Recurrent daily fevers, joint swelling, evanescent and salmon colored blanchable rash on trunk and proximal extremities that comes on with a fever and resolves on its own, may have serositis
Koebner phenomenon is related to which disorder? What is another name for this disease?
Cutaneous hypersensitivity following superficial trauma seen in sJIA aka Still’s disease.
Oligoarticular vs polyarticular JIA?
4 or less vs 5 or more joint involvement; need to check vision regularly with slit-lamp exam for oligo due to chronic uveitis (esp. if ANA+)