First Aid Rheum Flashcards

(35 cards)

1
Q

Joint findings in osteoarthritis

A

subchondral cysts, sclerosis, osteophytes, eburnation, Heberden nodes (DIP) and Bouchard notes (PIP)

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2
Q

Joints findings in rheumatoid arthritis

A

Pannus formation (MCP, PIP), subcutaneous rheumatoid nodules (fibrinoid necrosis), ulnar deviation of fingers, subluxation, baker cyst

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3
Q

Classic presentation of osteoarthritis

A

pain in weight-bearing joints after use, improves with rest, bowlegged, non-inflammatory, no systemic symptoms

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4
Q

Classic presentation of rheumatoid arthritis

A

morning stiffness lasting more than 30 minutes, improves with use, symmetric joint involvement, systemic symptoms

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5
Q

treatment of osteoarthritis

A

NSAIDs, intra-articular glucocorticoids

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6
Q

treatment of rheumatoid arthritis

A

NSAIDs, glucocorticoids, disease-modifying agents

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7
Q

disease modifying agents

A

methotrexate, sulfasalazine, TNF-alpha inhibitors

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8
Q

predisposing factors to osteoarthritis

A

age, obesity, joint deformity, trauma

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9
Q

predisposing factors for rheumatoid arthritis

A

female, +RF, anti-cyclic citrullinated peptide antibody more specific, HLA-DR4

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10
Q

Findings in Sjogren’s syndrome

A

xerophthalmia (decreased tear production/corneal damage)
xerostomia (decreased saliva production
SS-A (anti-Ro) and SS-B (anti-La) antinuclear antibodies
bilateral parotid enlargement

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11
Q

definition of sjogren’s syndrome

A

autoimmune disorder characterized by destruction of exocrine glands

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12
Q

Treatment of gout

A

Acute: NSAIDs, glucocorticoids, colchicine
Chronic: xanthine oxidase inhibitors (allopurinol, febuxostat)

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13
Q

overproduction of uric acid can be caused by

A

Lesch-Nyhan syndrome, PRPP excess, increased cellular turnover (cancer), von Gierke disease

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14
Q

diseases that may be associated with pseudogout

A

hemochromatosis, hyperparthyroidism, hypoparathyroidism

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15
Q

treatment of pseudogout

A

NSAIDs for sudden severe attacks; steroids; and colchicine

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16
Q

common causes of infectious arthritis

A

S. aureus, Streptococcus, and Neisseria gonorrhoeae

17
Q

Gonococcal arthritis presents as

A

migratory arthritis with an asymmetric pattern

synovitis, tenosynovitis, and dermatitis

18
Q

Seronegative spondyloarthropathies

A
HLA-B27: more often in males
psoriatic arthritis
ankylosing spondylitis
IBS
Reactive arthritis (Reiter syndrome)
19
Q

findings in psoriatic arthritis

A

asymmetric and patchy involvement, dactylitis (sausage fingers), pencil in cup deformity

20
Q

findings in ankylosing spondylitis

A

stiff spine due to fusion of joints, uveitis, aortic regurgitation, bamboo spine

21
Q

classic triage with reactive arthritis

A

conjunctivitis and anterior uveitis
urethritis
arthritis
“can’t see, can’t pee, can’t bend my knee”

22
Q

classic presentation of SLE

A

rash, joint pain, fever in females of reproductive age and of african descent

23
Q

treatment of SLE

A

NSAIDs, steroids, immunosuppressants, hydroxychloroquine

24
Q

sarcoidosis is characterized by

A

immune-mediated, widespread noncaseating granulomas and elevated serum ACE levels

25
sarcoidosis is associated with
restrictive lung disease, erythema nodosum, lupus pernio, bell palsy, epithelioid granulomas containing micrscopic SChaumann and asteroid bodies, uveitis and hypercalcemia
26
treatment of sarcoidosis
steroids
27
polymyositis
progressive symmetric proximal muscle weakness, characterized by endomysial inflammation with CD8+T cells (most often involves shoulders)
28
dermatomyositis
similar to polymyositis but also invovles malar rash, Gotron papules, heliotrope (erythematous periorbital) rash, perimysial inflammation and atropy with CD4+ T cells
29
Lab findings in polymyositis/dermatomyositis
increased CK, +ANA, +anti-Jo-1, +anti-SRP, + anti-Mi-2 antibodies
30
treatment of polymyositis/dermatomyositis
steroids
31
pathophysiology of myasthenia gravis
autoantibodies to postsynaptic ACh receptor
32
Scleroderma
excessive fibrosis and collagen deposition throughout the body
33
manifestations of scleroderma
sclerosis of skin, manifesting as puffy and taut skin with absence of wrinkles
34
diffuse scleroderma
widespread skin involvement, rapid progression, early visceral involvement anti-Scl-70 antibody (anti-DNA topoisomerase I antibody)
35
limited scleroderma
``` Calcinosis Raynaud phenomenon Esophageal dysmotility Sclerodactyly Telangiectasia (associated with antiCentromere antibody) ```