Autoimmune Flashcards
Fibromyalgia
Idiopathic, chronic, nonarticular widespread pain syndrome
- dx of exclusion*
Sxs:
- widespread msk pain* above/below waist on both sides >3 mo, radiating diffusely +/- arthralgia
- external stressors
- allodynia, fatigue, HA, IBS, insomnia, functional impairment
Dx: CBC, ESR, CRP, TSH, ANA, RF, Xray
Tx:
- pt ed: chronic, not progressive, not curable
- treat comorbidities: weight loss, mood, sleep
- exercise
- ADs: amitriptyline, duloxetine
- analgesics: tramadol, APAP, cyclobenzaprine
Gout General
Deposition of uric acid crystals throughout body
- MC acute monoarthritis
Hyperuricemia d/t:
- dec excretion (hereditary, diuretic, ETOH, renal disease, cyclosporine)
- inc production
- inc intake
Triggers: ETOH, trauma, diuretics, salicylates, allopurinol, contrast dye
Sxs:
- asx hyperuricemia 10-30y
- acute/intermittent gout: rapid onset exquisite pain a/w warmth, swelling, erythema; pain Inc over 8-12hr; +/- fever, chills
- intercritical period: asx period after flare w/crystals still forming
- chronic tophaceous gout: usually 10+ yr after onset; intercritical periods no longer pain free
Gout Dx/Tx
Dx
- hyperuricemia w/serum uric acid >7mg/dl (may be normal)
- CBC: leukocytosis w/Inc PMNs
- ESR/CRP: may be elevated
- definitive**: synovial fluid arthrocentesis - monosodium urate crystals under polarized light microscope
- GS/Cx r/o infection
Tx
- acute: NSAIDs until 1-2d after sx resolve [> colchicine > steroids]
- resolution, then maintenance: uric acid lowering tx + NSAID/colchicine
Uric acid lowering
- Xanthine oxidase inhibitor: allopurinol; if renal function good
- Uricase: pegloticase
Start maintenance if >2 attacks/yr, tophi present, urolithiasis
Comorbid disease: diet, ETOH, obesity
Pseudogout
- calcium pyrophosphate crystal deposition *
- intermittent monoarthritis in knee/wrist
Sxs:
- acute, monoarticular inflammatory arthritis lasting days-wks (50% knees)
- asx between episodes
- provoked by illness, trauma, surgery
- may cause progressive DJD, valgus deformity of knees, patellofemoral arthritis
Dx:
- synovial fluid analysis to differentiate from gout
- CPPD crystals**
- ESR/CRP may be elevated
Tx:
- same as gout
- colchicine daily useful for px, but doesn’t work as well compared to as with gout
- tx concurrent metabolic conditions
Polymyositis
MC 10-15y and 45-60y; women
Sxs: inflammatory myopathy + prox muscle weakness*
- interstitial fibrosis or pneumonitis (record baseline pulm fx, CXR)
- cardiomyopathy or CHF
Dx: Bx = T-cell mediated lymphocytic infiltrates*
- INC CK, aldolase, LDH
- EMG changes
- MRI: delineate muscle involvement to guide biopsy
Tx:
- prednisone taper 3-6mo
- MTX, AZA
Reactive arthritis (Reiter syndrome)
“can’t see, can’t pee, can’t climb a tree”
- spondyloarthritis following infection
Urethritis bugs: Chlamydia, Yersinia, Salmonella, Shigella, Campy, C. diff
Sxs:
- asymmetrical mono/oligo arthritis in LE
- enthesistis/dactylitis
- GU sx
- conjunctivitis, oral ulcers, rashes, nail changes, genital lesions
Dx:
- stool testing, chlamydia screening, HLA-B27, ESR/CRP, WBC
- imaging to r/o OA
Tx:
- NSAIDs
- glucocorticoids
- Abx for acute infection
Rheumatoid arthritis
Inc r/o MI, CVA, infection, NHL, osteoporosis
Sxs:
- symmetric joint pain, stiffness, swelling
- morning stiffness >1hr
- systemic symptoms
- other: synovitis, effusion, erythema, warmth, decreased ROM
Dx:
- positive RF, anti-CCP
- JFA: inflammatory
- Xray: eval for erosive changes
Tx:
- DMARDs: plaquenil, MTX, Leflunimide, sulfasalazine, AZA
[DMARDs require monitoring for: BM suppression, renal insufficiency and function]
- adjunct: NSAIDs, steroids
Systemic lupus erythematous General
Vascular: accelerated atherosclerosis = TIA, CVA, MI
May be drug induced - hydralazine
Manifestations
- skin: malar or discoid rash, oral/nasal ulcers; nonscarring alopecia, diffuse thinning
- synovitis in 2 joints or tenderness in 2 joints + 30 min morning stiffness
- serositis (lung or pericarditis)
- renal: nephritis, proteinuria, RBC cases, hematuria
- neuro: seizure, psychosis, mononeuritis multiplex
- hemolytic anemia
SLE dx/tx
Dx
- U/A: investigate nephritis
- leukopenia, lymphopenia
- ANA
- Anti-dsDNA, anti-Sm, APL-ab, low C’
- check LDH, haptoglobin, Coombs (hemolytic anemia)
- Pregnancy: monitor APS (anti-coagulation), SSA/SSB
- if SSA+, monitor baby for heart block between 18-24wk in utero
Tx:
- steroids for skin lesions
- aggressive mgmt of HLD, HTN, hyperglycemia (protect renal)
- non-lifethreatening: NSAIDs, low dose corticosteroid, hydroxychloroquil, MTX, mycophenolate, AZA
- organ involvement: prednisone, IV methylprednisolone, DMARDs, etc.
- SLE/preg: control sxs w/low dose prednisone, plaquenil, AZA
Lupus nephritis
Class II: microscopic hematuria, proteinuria
Class III: + HTN, dec GFR, +/- nephrotic syndrome; <50% of glomeruli affected
Class IV: MC and severe**
- low C’
- elevated dsDNA levels w/active disease
- > 50% glomeruli affected
Class V: diffuse thickening of glomerular capillary wall and subepithelial immune deposits
Tx:
- induction: glucocorticoids & cyclophosphamide OR mycophenolate mofetil
- maintenance: AZA OR mycophenolate mofetil