Antibody associated with diffuse systemic sclerosis
What is Scl-70
Vasculitis affecting upper and lower respiratory tract, kidney involvement. May have saddlenose deformity or septal perf, and eye ulcerations.
What is Wegner's/Granulomatosis with Polyangitis
A general finding on Radiographic imaging suggesting OA
What is joint space narrowing, subchondral bone sclerosis, subchondral cysts, and osteophytes
Type of crystals present in gout
What are Monosodium urate crystals
Antibody associated with MCTD
What is anti-RNP
High doses of glucocorticoids may be associated with which complication in Systemic sclerosis
What is renal crisis
MSK Condition associated with Giant Cell Arteritis
What is polymalgia rheumatica
2 joints in the hand affected by OA
What is the DIP, PIP, or thumb base (first carpometacarpal)
Most common joint involvement in Gout flare
What is first metatarsophalangeal joint/big toe/ podagra
Limited Cutaneous SSc has a better prognosis, but a higher risk of which complication versus Diffuse Cutaneous SSc
What is pulmonary arterial hypertension
Condition known as watermelon stomach, often associated with connective tissue diseases such as systemic sclerosis
What is GAVE/Gastric antral vascular ectasia syndrome
Granulomatous vasculitis of multiple organ systems, particularly the lung; characterized by asthma, peripheral eosinophilia, eosinophilic tissue infiltration; glomerulonephritis can occur. Heart involvement is the leading cause of death
Eosinophilic Granulomatosis with Polyangiitis (ChurgStrauss)
morning stiffness usually lasts what length in OA
Less than 30 minutes
What is pseudogout/ calcium pyrophosphate
Used to determine whether the eye produces enough tears to keep it moist. The test is performed by placing filter paper inside the lower lid of the eye.
What is Schirmer's test
The 5 components seen in a classic subset of Limited Cutaneous Systemic Sclerosis
CREST - Calcinosis, Raynaud's, esophageal dysmotility, Sclerodactyly, Telangiectasias
Vasculitis of the large arteries with strong predilection for aortic arch and its branches; most common in young women; presents with inflammatory or ischemic symptoms in arms, legs, head, and neck, systemic inflammatory symptoms, aortic regurgitation.
What is Takayasu Arteritis
noninflammatory condition characterized by calcification and ossification of spinal ligaments and entheses; radiographs usually show confluent “flowing” ossification of at least four contiguous vertebral levels, usually on the right side of the spine.
What is Diffuse idiopathic skeletal hyperostosis
Name 2 conditions associated with secondary CPPD
Primary Hyperparathyroidism, Hemochromatosis, Hypophos/mag, chronic gout, postmenisectomy, Gitelman's syndrome, epiphyseal dysplasias
Antibodies to for APS (cardiolipin, B2 glycoprotein, Prothrombin), should be tested one 2 occasions at least how many weeks apart
What is 12 weeks
Name 3 treatment options/modalities for catastrophic APS
What is anticoagulation, Steroids, Plasma Exchange, IVIG
Rare autoimmune systemic vasculitis associated with the following: inflammatory ocular manifestations, excess tear production, vision impairment, bilateral loss of hearing, and vestibular dizziness.
What is Cogan's Syndrome
Name 6 different modalities for treatment of OA
Weight reduction, physical therapy, bracing/orthotics, topical capsaicin, Tylenol, NSAIDs, Opioids, Intrarticular Glucorticoids, Hyaluronan (controversial benefit), Glucoasmine/chrondroitin (recommend against), Debridement/lavage (no benefit vs no treatment), joint replacement
destructive shoulder arthropathy due to the deposition of hydroxyapatite crystals, and identification of these crystals in synovial fluid is the cornerstone of diagnosis. No specific treatment, only supportive therapy is available
What is Milwaukee shoulder
Pregnancy morbidity from APS with thrombosis can be reduced by utilizing which 2 medications
What is low dose ASA + Heparin