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49 Cards in this Set

  • Front
  • Back
Ankylosing spondylitis
seronegative inflammatory arthritis; axial skeleton fusion and SI involvement; forward stooped posture with increased thoracic kyphosis and loss of lumbar lordosis
Schober test
used to test ROM of lower spine by measuring degree of forward flexion using 2 landmarks on patients back; positive in ankylosing spondylitis
Diffuse idiopathic spinal hyperostosis (DISH)
calcification on spinal ligaments due to abnormal osteoblastic activity; most common in thoracic spine (linear calcifications and ossification across at least 4 contiguous vertebral bodies)
Scheuermann kyphosis
idiopathic anterior wedging of vertebral body; thoracic and thoracolumbar spines=rigid kyphosis; wedging of >5 degrees and at least 3 adjacent vertebrae; pain worse after activity, better with rest
Stork test
stand on one leg and hyperextend back; pain elicited in spondylolisthesis
anti-cyclic citrullinated peptide antibodies
75% sensitivity and 90% specificity for RA
Rheumatoid factor
IgG autoantibodies against Fc portion; found in RA, SLE, Sjogren's, hepC
Discoid lesions
erythematous raised patches with adherent keratosis scaling-extend into dilated hair follicles; occur in 25% SLE on face, neck and scalp-slowly expand with active inflammation on periphery
histology of Rheumatoid nodule
central necrosis surrounding by pallisading macrophages and lymphocytes; test positive for RF
Gottron's papules
erythematous to violaceous papules that occur symmetrically over exstensor aspect of metacarpophalangeal and interphalangeal joints; may scale and ulcerate; hallmark of dermatomyositis
heliotrope eruption
erythematous eruption located on upper eyelids with edema; found in dermatomyositis
anti-smith antibodies
55-100% specific for SLE; non-histone proteins that interact with RNA; detected in 10-50% SLE; do not correlate with extent of disease (like anti-dsDNA)
anti-phospholipid antibodies
100% specific for SLE; present in ~1/3 SLE
Anti-Jo-1 antibody
specific in inflammatory myopathies (polymyositis and dermatomyositis)
Anti-Ro antibodies
Sjogren's 57%; also seen in SLE, systemic sclerosis, RA, and primary biliary sclerosis
anticentromere antibodies
CREST/scleroderma
anti-Scl-70 (antitopoisomerase I)
96% specific for scleroderma (associated with diffuse form=high risk of lung disease)
limited scleroderma (CREST syndrome)
affects hands, arm, and face; calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangectasia
diffuse scleroderma
organ involvement plus skin; 90% Raynaud's
iron studies in thalassemia
normal to high ferritin and normal to low TIBC; target cells
kidney in SLE
thickened capillary walls (tram-track, then wire-loop)=membranous glomerulonephritis; cortical surface looks flea-bitten
T-score osteopenia and osteoporosis
T-score of -1 to -2.5 and <-2.5 respecitively
fibromyalgia dx
pain in all 4 quadrants of body for >3 months and at least 11 of 18 tenderpoints
polymyalgia rheumatica
severe aching and stiffness in neck, shoulders, and pelvis; no loss of strength; association with temporal arteritis
elevated enzymes in dermatomyositis
CK and aldolase; associated w/ malignancy
Tx sicca syndrome
pilocarpine=muscarinic agonist that stimulates all 3 muscarinic receptors and enhances oral/ocular secretions; lacks arthritis (unlike Sjogren)
xerostomia and xerophthalmia
dry eyes and dry mouth
Complex regional pain syndrome
pain, swelling, limited ROM, vasomotor instability, skin changes, patchy bone demineralization; often begins after injury
Complex regional pain syndrome stage 1
dvlp pain in limb; burning/throbbing, sensitivity to touch/cold, localized edema; vasomotor disturbances; x-ray normal, possible patchy bone demineralization
Complex regional pain syndrome stage 2
progression of soft tissue edema, thickening of skin, muscle wasting; 3-6 months
Complex regional pain syndrome stage 3
decreased ROM, contractures, waxy trophic skin, brittle ridged nails, severe bone demineralization
Complex regional pain syndrome type 1 vs 2
1=no definable nerve lesion; 2=definite peripheral nerve injury present
Reactive arthritis (aka Reiter disease)
aseptic inflammatory polyarthritis; mostly young males; urethritis, conjuntivitis, and arthritis; usually follows STD or enteric infection=Shigella, Campylobacter, salmonella, chlamydia
enthesitis
inflammation around the bone where ligaments, tendons, and joint capsules insert (especially achilles tendon area)
Rx C trachomatis
macrolide or tetracycline (doxy)
Raloxifene specs
mixed agonist (bone)/antagonist (breast/vaginal tissues); increases risk of thromboembolism, breast cancer risk decreases, no effect on endometrial cancer (like tamoxifen)
Chronic fatigue
persistent/relapsing fatigue>6 months unexplained and not alleviated by rest
hydralazine
first line anti-hypertensive in pregnancy; causes drug induced lupus
causes of drug induced lupus
hydralazine, procainamide, quinidine, isoniazid, diltiazem, minocyline
syndesmophytes
bony growths inside ligaments; seen in ankylosing spodylitis
enthesophytes
bony projections forming at attachment site for tendons or ligaments formed in response to repetitive stress
Whipple's disease
gram-pos bacteria; fevers, GI symptoms, joint pains (malabsorption, foul-stools, GI bleeding); tropical
porphyria cutanea tarda
deficient uroporphyrinogen decarboxylase; blistering of hands, forearms and face-worse in sunlight
what precipitates gouty attacks
purine-rich substances: alcohol, high protein meals (fish, mussels, meats (organ meats more so)), medicines (thiazide diuretics)
osteopetrosis
marble bone disease; failure of bone resorption leading to thickening, dense bones prone to fracture-secondary to abnormal osteoclast fxn; serum Ca, phosphate, and ALP normal; erlenmeyer flask deformity on xray
polymyositis
progressive, systemic CT disorder; 50-70 yo females; increased CK, aldolase, and positive anti-Jo-1-antibodies; Rx high dose corticosteroids or azathioprine and/or methotrexate
Felty's syndrome
rare, severe subset of RA=RA, splenomegaly, granulocytopenia
Caplan syndrome
combo of RA and pneumoconiosis that manifests as intrapulmonary nodules
neonatal exposure to anti-Ro/SSA or Anti-La/SSB antibodies
increases risk of neonatal SLE and causes 60-90% cases of congenital complete heart block=bradycardia, intermittent cannon waves in neck and gallops/murmurs; highest prevalence in Sjogrens