Rheumatology Review Flashcards

1
Q

fill out this flow chart

A
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2
Q

lab factors that make you think it’s RA

A

rf factor and Anti-CCP

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3
Q

for RA:
• Swelling and tenderness in ___ joints of
___ and __ are most common
presentation

• Symptoms present for > ___weeks with > ___joints and prolonged ___ stiffness
should make you consider RA

A

• Swelling and tenderness in small joints of
hands and feet are most common
presentation • Symptoms present for > 6 weeks with > 3
joints and prolonged morning stiffness
should make you consider RA

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4
Q

what part of this picture would. make you think it’s RA rather that OA

A

small joint swelling appearnace is common in both, but OA also has large joint involvement. OA is also less symmetrical, where as in RA, both hands are likely to b affected at the same time.

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5
Q

which diseases are causing each pattern of arthritis?

A
  1. RA= symmetric, affecting small joints and the knees
  2. Psoriatic: very asymmetric
  3. ankylosing spondylitis: spondilitis/axial involvement and large peripheral joints in an asymmetrical fashion.
  4. Osteoarthritis: affected some small joints in the hands but LARGE ones too like knees, hip, big toe (compared to MCP)
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6
Q

out of RA, psoriatic arthritis, AS and OA, which one has a more symmetrical presentation?

A

RA. the rest have fewer joints being affected at once (usually) and are often asymmetrical.

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7
Q

which one is more likely to be OA vs RA

A

left = OA = bony prominence– it’s hard

right = synovial swelling = RA. Inflammation is soft.

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8
Q

•  3 swollen joints

  • MTP/MCP involvement
  • Positive squeeze test

• Morning stiffness> 30 mins

most likely diagnosis

A

rheuamtoid arthritis

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9
Q

how would these lab values look in someone with RA?

A
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10
Q

Bouchard nodes affect ___ joints in OA, and heberdens nodes affect ____ joints in OA

A

treat OA with acetaminophen and nsaid pain relief

  • Bouchard = pip
  • heberden = dip
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11
Q

management of OA

A

weight managmenet

light exercise (activity may increase the pain but certain activities might help strengthen areas)

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12
Q

T/F ANA is good for lupus detection screenign

A

false. • The ANA test is not specific to a single disease. It should NOT be used as a
screening test
• A strongly positive ANA test means that it is more likely that a person may have an autoimmune disease. However, positive test results do not tell what type of autoimmune disease it is.

if you suspect lupus, check an ENA profile and anti-smith or anti-dsDNA

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13
Q
A
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14
Q

note:

A
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15
Q
A
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16
Q

what types of arthritis comprise seronegative classifications

A

AS

psoriatic arthritis

reactive arthritis

IBD related or enteropathic arthritis

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17
Q
A
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18
Q

what part of the body does spondyloarthritis (rF negative) affect?

A

spine

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19
Q

what is spondyloarthritis?

• Group of diseases with chronic inflammatory arthritis predominantly affecting the _____

  • variable peripheral joint disease that is often ___, involving oligoarthritis of ___ joints and associated with extra articular manifestations such as (___, ___ and ___)
  • usually ____ and _____ antibody negative.
  • assocaited with the ____ gene
A

what is spondyloarthritis?

• Group of diseases with chronic inflammatory arthritis predominantly affecting the spine

  • variable peripheral joint disease that is often asymmetrical, involving oligoarthritis of large joints and associated with extra articular manifestations such as ibd, psoriasis, and iritis
  • usually rf and anti-ccp antibody negative.
  • assocaited with the hla-b27 gene
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20
Q

what type of arthritis does this person have

A

psoriatic arthritis. it’s an inflammatory seronegative arthritis associated with psoriasis. 30% of people with psoriasis have arthritis

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21
Q

associated features and comorbidies of psoriatic arthritis

A

associated features; dactylitis, asymmetric joints affected involving the spine, plaque psoriasis, enthesitis, uveitis and IBD

comorbidites: CVD, diabetes, NAFLD, depression

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22
Q

Patients with ____ disease more likely to develop PsA

A

Patients with nail disease more likely to develop PsA4

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23
Q

usual sites of enthesitis

A
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24
Q

dactylitis is associated with which types of arthritis?

A

psoriatic arthritis and reactive arthritis

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25
Q

eye problems associated with psoriatic arthritis

A

uveitis and iritis– make sure to ask about pain, redness and reduced vision

26
Q

nail matrix vs nail bed disease

A

nail matrix: pitting, leuconychia, crumbling red sponts in the lunula

nail bed disease: onycolysis, subungual hyperkeratosis, oil drop change, splinter hemorrhages

27
Q

what radiographic findings would you see in PsA

A

pencil in cup change in severe disease

sacroilitis

syndesmophytes; may look like ankylosing spondylitis

28
Q

why might liver enzymes be elevated in PsA

A

because of NAFLD

29
Q

treatment of PSA

A

NSAIDS

methotrexate (is 3 joints or more)

biologics

may use glucocorticoids for flares or as bridging therapy

30
Q

T/F Ankylosing spondylitis is worse with rest and better with movemnet

A

true. it’s an inflammatory joint issue.

31
Q

clinicical criteria for AS

A
  1. low back pain and stiffness for more than 3 months that improves with exercise
  2. limitation of motion of the lumbar spine in both the sagittal and frontal planes
  3. limitation of chest expansion relative to normal values correlated for age and sex
32
Q

for mechanical low back pain, 25% of patients will notice improvement in symptoms with _____. These patients will have symptoms that improve with ____therapy

A

for mechanical low back pain, 25% of patients will notice improvement in symptoms with ACTIVITY. These patients will have symptoms that improve with PHYSIOTHERAPY

33
Q

two tests to look for AS

A

schober test and occipt to wall test

34
Q

usual presenting symptoms for AS

A

back pain

enthesitis

stiffness

peripheral joint pain

decreased spinal mobility

back questionmark formate

fatiguw

weightloss

iritis, IBD, symptoms of assocaited diseases.

35
Q

outline the typical CBC, creatining, nsaid use, CRP/ESR and HLAB27 findings of AS

A
36
Q
A

baboo spine – longstanding untreated AS– fused SI joints

37
Q

T/F We should perform a whole body bone scan if we suspect AS

A

false. also, don’t order an HLA-B27 unless spondyloarthritis is suspected based on specific signs or symptoms.

38
Q

treatment of AS

A
  • treatment usually starts with physiotherapy and NSAIDS
  • if AS doesn’t respond to NSAIDs, can try a biologic
39
Q

T/F DMARDS can be prescribed forAS

A

false. DMARDS usually don’t work on inflammatory spinal disease. We try to treat AS with NSAIDS and biologics

40
Q

Enteropathic arthritis is often indistinguishable from ______, usually follows onset of ___ ___, and has ___ correlation between bowel and joint flares

A
41
Q

which sex is affected more by reactive arthritis?

A

male.

  • follows infectious diarrhea
  • Salmonella, Yersinia, Shigella, Campylobacter
  • also associated with urogenital infections
  • Chlamydia (can be asymptomatic)

• bacteria not identified in most patients

42
Q

triad in reactive arthritis

A
  1. urethitis
  2. conjunctivitis
  3. arthritis.

reiters triad.

plus or minus fever, malaise, fatigue and weightloss and DSCTYLITIS AND ACHILLES ENTHESITIS

43
Q

• 65 year old male with Crohn’s disease on
Vedolizumab.

• Seronegative rheumatoid arthritis
currently on sulfasalazine 1000 mg bid.

• Awaiting Left TKR secondary to OA

• Asked for follow-up with rheumatology
pre-operatively regarding medications.

• Anesthesia did not order a C-spine in their
recommendations.

IS THIS RA?

A

IBD red flag, seronegative makes RA less likely.

Schober test is 15 cm usually, this guy’s did not change. He has a stooped posture. AS

44
Q

note

A
45
Q

skin characteristics of dermatomyositis

A

heliotrope rash– muscle weakness, normal EMG but elevated ESR

gottrons rash on PIPs

Shawl sign

46
Q

therapy for dermatomyositis

A
47
Q

sjogrens syndrome symptoms

A

it’s a disease Characterized by lymphocytic infiltrates of salivary and tear glands leading to oral/ocular dryness and by antibody secretion arthritis

dry mucosa

arthritis

fever/fatigue

lung inbolbement

kidney involvement

raynauds

48
Q

___ ___/ ____ is a chronic multisystem disease characterized by
widespread vascular dysfunction and progressive
fibrosis of the skin and internal organs.

The diagnosis
of___ and related disorders is based primarily upon
the presence of characteristic clinical findings and
supported by specific serologic abnormalities.

A

SYSTEMIC SCLEROSIS/SCLERODERMA is a chronic multisystem disease characterized by
widespread vascular dysfunction and progressive
fibrosis of the skin and internal organs. The diagnosis
of SSc and related disorders is based primarily upon
the presence of characteristic clinical findings and
supported by specific serologic abnormalities.

49
Q

symptoms of limited scleroderma vs diffuse cutaneous systemic sclerosis

A

Limited cutaneous systemic sclerosis – Skin sclerosis is typically distal to the elbows and knees, and, to a lesser extent, the face and neck, while the trunk is spared.

Many patients with limited cutaneous SSc (lcSSc) have manifestations of
the CREST syndrome (Calcinosis cutis, Raynaud phenomenon, Esophageal
dysmotility, Sclerodactyly, and Telangiectasia).

Diffuse cutaneous systemic sclerosis – Skin thickening extends proximally to the upper arms, thighs, and/or trunk.

Analysis of a large patient cohort indicates that many patients with SSc cannot readily be classified into lcSSc or diffuse cutaneous SSc (dcSSc), and multiple distinct
additional disease subsets with shared features may exist

50
Q

scleroderma antibodies that should be screened when suspecting scleroderma

remember; clinical features are broad
• Skin Manifestations – universal
• Raynaud’s phenomenon
• Arthritis, tendonitis, tendon friction rubs • GI involvement: dysphagia, diarrhea,
reflux
• Pulmonary involvement: Interstitial lung
disease, pulmonary arterial hypertension
• Cardiac involvement • Renal involvement • Neuromuscular involvement • Genitourinary involvement • Cancer risk

A
51
Q

scleroderma treatment

A

often treating the symptoms individual

raynauds; vasofilators such as calcium channel blockers, prostaglandins

for renal fibrogenesis; new therapies targeting the fibroblasts focusing on growth factors

for abnormal immune response Scl-70: immunosuppresive drugs like prednisone, mycophenylate and cyclophosphamide

52
Q

classification of vasculitis

A
53
Q

when to expect vasculitis

A
  • chronic and recurrent headches
  • muscle weakness, ischemia, claudication of jaw or extremities
  • palpable purpura
  • mononeuritis multiplex
  • TIA/stroke/neurological symptoms-wrist drop
  • kidney dysfunction- glomerular nephritis, hematuria, proteinuria
  • lung problems– pleuritis, alveolar hemorrage
  • cardiac issues/aortic aneurysm/angina
54
Q

specific antibody consisent with SV vasculitis

A

ANCA

55
Q

lab investigations for GPA

A
56
Q

note for GPA vasculitis

A
57
Q

a person presents with proximal muscle pain, weakness and morning stiffness. they are 60 years old. they are unabble to raise arms due to weakness. what is going on?

A

polymyalgia rheumatica. this isn’t a vasulitis but it can lead to temporal arteritis or RA.

58
Q

what lab findings are consistent with polymyalgia rheumatica

A

elevated ESR above 40

  • normal muscle enzymes and creatining

normal EMG

may have ACD

no auto-antibodies

59
Q

management of polymyalgia rheumatica

A

prednisone until ESR is normal

  • watch for RA appearance after tapering
60
Q

immunologic criteria for lupus

A

low complement

firect coombs test

ana

anti-DNA

Anti-Sm

61
Q

____ vasculitis (____) is a specific type of cutaneous small-vessel vasculitis occurring in children and adults. It is characterized by palpable purpura in dependent areas such as the legs, and buttocks.

Consider the diagnosis of ____ vasculitis for any patient presenting with widespread palpable purpura, arthralgias of the ___ and ___, and ____ abdominal pain and/or an abnormal ___.

A

Immunoglobulin A vasculitis (IgAV) is a specific type of cutaneous small-vessel vasculitis occurring in children and adults. It is characterized by palpable purpura in dependent areas such as the legs, and buttocks.

Consider the diagnosis of IgA vasculitis for any patient presenting with widespread palpable purpura, arthralgias of the knees and ankles, and colicky abdominal pain and/or an abnormal urinalysis.