Rhuem Flashcards

1
Q

Negatively birefrigent crystals

A

Gout

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2
Q

Positively birefrigent crystals

A

Pseudogout (calcium pyrophosphate crystals)

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3
Q

Treatment of primary angiitis of the CNS

A

High dose steroids and cyclophosphamide

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4
Q

Triad bilateral hilar lymphadenopathy, arthritis and erythema nodosum

A

Lofgren syndrome - diagnostic of sarcoidosis, no further testing needed

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5
Q

IgA Vasculitis diagnosis

A

Biopsy most accessible organ - usually skin. Will demonstrate leukocytoclastic vasculitis with heavy deposits of IgA and complement on immunofluorescent staining

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6
Q

Allopurinol hypersensitivity risk factors

A

CKD, diuretic use, Thai, Han Chinese and Korean descent

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7
Q

Testing for allopurinol sensitivity

A

HLA-B*5801 allele

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8
Q

Treatment of Ankylosing spondylitis

A

NSAIDs first line. TNF inhibitors second line, then sulfasalazine

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9
Q

Erythematous, macular patchy eruption sometimes with desquamation. Malar rash

A

Acute cutaneous lupus erythematosus

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10
Q

Photosensitivity rash on arms, neck and face. Annular/polycyclic or patchy papulosquamous

A

Subacute cutaneous lupus erythematosus

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11
Q

Hypo or hyper pigmented patches or plaques with erythema during active disease. Skin can become atrophic or hyperkeratotic with scarring

A

Discoid lupus erythematosus

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12
Q

Hypertensive emergency, rising Cr, microangiopathic hemolytic anemia and proteinuria in a patient with scleroderma

A

Scleroderma Renal Crisis

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13
Q

Treatment for scleroderma renal crisis

A

ACEi - titrate to blood pressure goal. Continue even in setting of rising Cr

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14
Q

Fever, erythema/warmth in superficial bursae with high WBC (>3000 with >50% PMNs) from bursal fluid +/- positive gram stain

A

Acute septic bursitis

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15
Q

Characteristic finding with HSP

A

leukocytoclastic vasculitis caused by IgA immune complexes within affected organs.

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16
Q

Does RF have to be positive to diagnose rheumatoid arthritis?

A

No! RA diganosis is based on clinical features consistent with symmetric polyarticular joint pain/stiffness and evidence of systemic inflammation. At diagnosis about 50% of patietns have an elevated RF, and 75-80% will develop a positive at some point in their course of disease.

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17
Q

Clinical tests in diagnosing akylosing spondylitis

A

Chest expansion test - normal is ability to expand the chest wall > or = 5 cm after maximum forced expiration. Expansion < 2.5cm is considered abnormal.
Limitation of lumbar spine motion in frontal and sagittal planes.

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18
Q

Atypical degenerative joint disease (involving 2/3/4 MCP joints), liver function abnormalities, diabetes

A

Suggestion of hemochromatosis as a cause

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19
Q

Ottawa ankle rules for malleolar zone

A

Xray ankle if pain at malleolar zone AND tender at posterior medial malleolus or posterior lateral malleolus or unable to bear weight 4 steps

20
Q

Ottawa ankle rules for midfoot zone

A

Xray foot if pain at midfoot zone AND tender at navicular or tender at base of 5th metatarsal or unable to bear weight 4 steps

21
Q

DIP arthritis and arthritis mutilans (deforming and destructive arthritis) with pencil in cup formation on XRAY

A

Psoriatic arthritis. Up to 30% of patietns can present with arhtritis PRIOR to psoriasis rash

22
Q

Positive serologies for systemic sclerosis

A

ANA, anti-topoisomerase 1 (ant-SCL-70) antibody, anticentromere antibody

23
Q

What should you screen for in a younger patient presenting with pseudogout?

A

Hemochromatosis

24
Q

Plain radiographs demonstrating lytic/sclerotic lesions (often in skull, throacic/lumbar spine and pelvis) with elevated alk phosphatase

A

Paget Disease

25
Next step after diagnosis of Paget Disease
Should bone scan to determine extent and distribution of disease. Then if asymptomatic can treat with bisphosphonates
26
Groin pain on weight bearing, limited internal rotation, steroid use, normal vital signs/infalmmatory markers
Avascular necrosis
27
Prognostic factors that are predictive of more severe erosive disease in RA
positive anti CCP Ab with higher titers, involvement of higher number of joints, positive RF and anti CCP Ab elevated ESR and CRP, persistent joint inflammation > 12 weeks
28
Stroke or VTE in a young patient without obvious risk factors and a prolonged PTT and thrombocytopenia
Suspicious for antiphospholipid syndrome
29
Antibodies to DNA histone complex
Drug induced lupus
30
Antibodies to dsDNA and Sm
SLE
31
Antibodies to RNA polymerase II/III and scl-70/anti-topoisomerase I
Systemic Sclerosis
32
Antibodies to RNP
MCTD
33
Antibodies to Sjogren's syndrome
SS-A/Ro, SS-B/La
34
Antibodies to centromere
LImited scleroderma
35
Antibodies to aminoacyl-tRNA synthetases (Jo-1)
polymyositis, dermatomyositis
36
Antibodies to myeloperoxidase
microscopic polyangitis
37
Antibodies to proteinase 3
granulomatosis with polyangittis
38
Proximal muscle weakness, myalgia and neuropathy in CKD patients with gout with elevated CK and cytoplasmic vacuolization on muscle biopsy.
Colchicine neuromyopathy
39
Test to determine between primary and secondary raynaud's
nailfold capillary examination - put oil on naifold and look at with an ophthalmoscope
40
Rheumatoid arthritis, neutropenia and splenomegaly
Felty syndrome
41
PAtients with dermatomyositis and polymyositis are at a fivefold increased risk of what?
Malignancy - they should have age approrpiate cancer screening, but also CT chest, abd, pelvis, UA for hematuria, serum CA125 and CA19-9, PSA, and EGD
42
Palpable purple, arthralgias, membranoproliferative glomerulonephritis, low serum complement, cutaneous vasculitis and neuropathy. False positive ANA and RF
Mixed (type 2) cryoglobulinemia due to Hep C
43
Things to consider in a patient presenting with clubbing of the fingers (even with underlying lung disease) AND synovitis of knees, ankles and fingers
Hypertrophic osteoarthropathy - abnormal proliferation of skin and osseous tissues usually due to an intrathoracic process frequently non-small cell lung cancer
44
Patient with long standing RA presenting with neck pain radiating to occipital region, slowly prgoressive spastic quadriparesis, painless sensory deficits in hands/feet, respiratory dysufnction
Consider RA cervical myelopathy - occurs due to atlanto-axial subluxation (C1-C2)
45
Methotrexate toxicities
Fever and GI distubrances with days of MTX dose. Macular rash. Stomatitis and megaloblastic anemia (these two are due to folic acid inhibition and can be treated with supplementation)
46
Subacute shoulder arthropathy with hemorrhagic effusion. Xrays show periarticular calcification and destructive arthritis
Basic calcium phosphate deposition (milwaukee shoulder)