Rheumatology Flashcards

1
Q

Treatment of dermatomyocytis

A

1st line treatment is prednisone, if no response can use azathioprine or methotrexate in addition, last line is immunoglobulin

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2
Q

Modifiable risk factor for RA

A

Smoking increases the risk of RA

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3
Q

Lofgren syndrome

A

Sarcoid presenting as: fever, erythema nodosum, polyarthralgia and hilar lymphadenopathy. Do not need tissue diagnosis

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4
Q

Heerfordt syndrome

A

Sarciod presenting as: uveitis, parotid enlargement, and fever. Do not need tissue diagnosis

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5
Q

Gout or infected joint?

A

They can occur at the same time. Suspect infection if the synovial leukocyte count is >50,000

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6
Q

Treatment of RA, 2nd agent

A

If patient fails methotrexate start combination therapy by adding a TNF-alpha inhibitor.

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7
Q

Treatment of ankylosing spondylitis

A

First line treatment is routine use of NSAIDs. If not tolerated then TNF-alpha inhibitors. Nonbiologic DMARDs are NOT effective in axial disease

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8
Q

Inclusion body myositis

A

Most common form of myositis >60, men
Proximal and distal muscle weakness
CK is modestly elevated
No extramusclar manifestations

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9
Q

Polymyositis

A

Younger patients, women
Proximal muscle weakness
Extramuscular manifestations are common
Tend to have positive auto-antibodies (80% +ANA)

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10
Q

Type I cryoglobulinemic vasculitis

A
Monoclonal immunoglobin, paraprotein
Seen in patients with Sjogrens, Waldenstrom and multiple myeloma 
Palpable purpura
Mononeuritis multiplex
Immune complex glomerulonephritis
low C3 and C4
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11
Q

Type II cryoglobulin vasculitis

A

Most commonly occurs in active hep C infection
Palpable purpura
Mononeuritis multiplex
Immune complex glomerulonephritis

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12
Q

RA developing SLE symptoms?

A

Drug induced lupus can occur with the TNF-alpha inhibitors (etnercept)

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13
Q

Mangement of SLE in pregnancy

A

Okay to use hydroxchloroquine. If have severe disease okay to have azathioprine if necessary. Prednisone for flare

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14
Q

Treatment of systemic sclerosis

A

MSK features are best treated with MTX

Alveolitis with cyclophosphamide

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15
Q

Management of arthritis associated with IBD

A

Start with sulfasalazine if NSAIDs worsen bowel symptoms.

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16
Q

Anti-UI ribonucleoprotein antibodies (RNP)

A

mixed connective tissue disease

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17
Q

Antiproteinase-3 antibodies

A

produce cANCA pattern and associated with granulomatosis with polyangiitis

18
Q

HSP

A

Small vessel vasculitis, palpable purupura, arthritis, abdominal pain and hematuria. Leukocytoclastic vasculitis with IgA deposits

19
Q

Microscopic polyangiitis

A

Small vessel vasculitis, +p-ANCA and antimyeloperoxidase antibodies , pulmonary involvement, glomuerulonephritis and purpuric skin lesions

20
Q

Polyarteritis nodosa

A

Medium vessel vasculitis, Mononeuritis multiplex, HTN, testicular, abdominal pain, look for hep B

21
Q

Granulomatosis with polyangiitis

A

Small vessel vasculitis, AKA Wegener, upper airway, mononeurititis multiplex, + c-ANCA (antiprotenase-3 antibody), pulmonary, ocular and renal disease

22
Q

Testing in myasthenia

A

most patients are acetylcholine receptor antibody +, some are MuSK +, get a chest CT to look for thymic hyperplasia or thymoma

23
Q

Reactive arthritis

A

Inflammatory arthritis that starts within 2 months of bacterial gastroenteritis or non-gonococcal urethritis/cervicitis. Can also have conjunctivitis. NSAIDS and steroids are the go to. If not effective try sulfasalazine

24
Q

Paroxysmal nocturnal hemoglobinuria

A

Unprovoked venous clots. Hemolytic anemia. Mild to moderate pancytopenia. Diagnose by flow cytometry showing that erythrocytes and lymphocytes do not have CD55 and CD59

25
Dx of ankylosis spondylitis
MRI of sacroilliac with contrasts (appears here first before lumbar spine)
26
Management of hereditary or acquired angioedema
- acute episodes can give IV CI inhibitor concentrate - chronic use danazol and stanozol which increase hepatic synthesis of C1 esterase inhibitor - epinephrine is NOT effective
27
Combined variable immunodeficiency, when to think about and what tests?
- frequent recurrent infections, encapsulated organisms, diarrhea - obtain Ig levels, if low see response to tenatus (protein) and pneumococcal (polysac) vaccination
28
Vitamin D supplementation
- D2 and D3 are converted in the liver to 25-D3 which is then converted to active 1-25 D3 by the kidney - so in liver disease give 25-D3 supplementation and kidney give active calcitriol - if liver and kidney okay can give D2 or D3 supplementation
29
Hand OA
effects DIP, PIP and first carpometacarpal joint, does NOT effect MCP
30
Hand RA
effects PIP and MCP joints, does NOT effect DIP
31
Arthritis of 2nd and 3rd MCP and PIP joints?
Think hemochromatosis
32
Sjogren syndrome at risk for?
B cell lymphoma
33
Hypertrophic osteoarthropathy
- see proliferation of skin and osseous tissues at the distal extremities - new periosteal bone formation seen on films - can have swelling - associated with lung cancer, chronic pulmonary infections and cardiac shunts
34
Systemic sclerosis antibodies
Diffuse: anti-scl-70 Limited: anti-centromere
35
Eosinophilic fasciitis
Woody induration of the skin sparing the hands and feet. NO Raynaud phenomenon
36
Anti–Jo-1
Associated with polymyocyitis and lung involvement
37
Anti–Mi-2
associated with dermatomyocytis rash, good prognosis
38
Familial Mediterranean fever
Fever, serosistis, arthritis and rash. Elevated inflammatory markers, positive serum amyloid A protein. Treat with colchicine
39
Anti-centromere pattern of ANA
CREST
40
Anti-smooth muscle antibody
autoimmune hepatitis
41
Anti-histone antibody
Drug induced SLE
42
Hypercalcemia in sarcoid
- treat with prednisone