Rheumatology Flashcards
Holster sign
Poikilodermic rash on the holster area seen with dermatomyositis
Most specific antibody for SLE
Anti-Smith
Antiribosomal P
Associated w/ CNS lupus and lupus hepatitis
Antibody in drug-induced lupus
Antihistone antibodies
Unusual RA findings
Hip- axial migration of femoral head into acetabulum
Knee-Tricompartmental joint-space narrowing
Ankle/mid-foot-Flat feet
Elbow joint- Difficulty w/ hand pronation/supination
Ulna-Loss of ulnar styloid
Rheumatoid nodules
Typically seen on olecrenon; can be manifested by MTX or leflunomide; helped by plaquenil and colchicine
Rheumatoid effusion
Characteristically has mononuclear WBCs unlike w/ infection
Cricoarytenoid athritis
Hoarseness, sore throat, dysphagia, and stridor seen commonly w/ RA and can present problem w/ intubation
Order of drugs to start for Fibromyalgia
- Duloxetine
- Pregabalin
- Milnacipran
Digital Pitting
Can be seen in patients w/ chronic Raynaud’s
Also more common in patients who have an underlying cause for their Raynauds (in contrast to idiopathic)
Chronic cutaneous lupus erythematosis
“Discoid variant”
Slowly progressive infiltrative plaques, scaly papules, or atrophic red plaques on sun exposed surfaces
Can appear verrucous
Only 10% will develop SLE
Subacute cutaneous lupus erythematosis
Papulosquamous, annular, or polycyclic rash that spares the face that can appear almost like psoriatic plaques
25% will develop SLE
Acute cutaneous lupus erythematosis
Butterfly rash that is invariably associated w/ SLE
Subcranial Giant Cell Arteritis
GCA affecting the large vessels of the chest (and sparing the temporal artery) causing UE claudication and aortitis
Can progress to HF, aortic root dilation, or aortic regurgitation if left untreated
**TO DIFFFERENTIATE FROM TAKAYUSU ARTERITIS, USE PATIENT AGE AS THIS DISEASE OCCURS EXCLUSIVELY IN PTS >50
Tocilizumab ADRs
Bowel perforation w/ history of diverticulitis
Also transaminitis, HLD, pancytopenia
Things to do prior to starting DMARD therapy
Update vaccinations
Screen for hepatitis, HIV, TB
Immune Mediated Necrotizing Myopathy (IMNM)
Prominent myonecrosis on bipap with RAPID onset of weakness; no dermatological manifestations
Anti-HMG coA reductase antibodies typically present or anti SRP
Inclusion body myositis
Cricopharyngeal weakness =» aspiration risk and dysphagia
Patients also typically have asymmetrical involvement of muscle weakness
Level to check when highly suspicious of inflammatory myopathy but CK is normal
Aldolase
Other cause common in USA for gout
High fructose corn syrup (sodas)
Specific US sign for gout
” Double Contour Sign”
Antihypertensive with mild uruicosuric effects
Losartan
Length of time for NSAID/colchicine prophylaxis for patients starting urate-lowering therapy
3 months after target serum levels are reached
Hypersensitivity Vasculitis
Palpable purpura that appear approximately 7 days after the offending antigen
Biopsy w/ immunofluorescence shows leukocytoclastic vasculitis w/o IgA deposits (unlike in IgA vasculitis)
Tx: Remove antigen =» resolves in 1 month