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
eye problems associated with psoriatic arthritis
uveitis and iritis-- make sure to ask about pain, redness and reduced vision
26
nail matrix vs nail bed disease
nail matrix: pitting, leuconychia, crumbling red sponts in the lunula nail bed disease: onycolysis, subungual hyperkeratosis, oil drop change, splinter hemorrhages
27
what radiographic findings would you see in PsA
pencil in cup change in severe disease sacroilitis syndesmophytes; may look like ankylosing spondylitis
28
why might liver enzymes be elevated in PsA
because of NAFLD
29
treatment of PSA
NSAIDS methotrexate (is 3 joints or more) biologics may use glucocorticoids for flares or as bridging therapy
30
T/F Ankylosing spondylitis is worse with rest and better with movemnet
true. it's an inflammatory joint issue.
31
clinicical criteria for AS
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
for mechanical low back pain, 25% of patients will notice improvement in symptoms with \_\_\_\_\_. These patients will have symptoms that improve with \_\_\_\_therapy
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
two tests to look for AS
schober test and occipt to wall test
34
usual presenting symptoms for AS
back pain enthesitis stiffness peripheral joint pain decreased spinal mobility back questionmark formate fatiguw weightloss iritis, IBD, symptoms of assocaited diseases.
35
outline the typical CBC, creatining, nsaid use, CRP/ESR and HLAB27 findings of AS
36
baboo spine -- longstanding untreated AS-- fused SI joints
37
T/F We should perform a whole body bone scan if we suspect AS
false. also, don’t order an HLA-B27 unless spondyloarthritis is suspected based on specific signs or symptoms.
38
treatment of AS
- treatment usually starts with physiotherapy and NSAIDS - if AS doesn't respond to NSAIDs, can try a biologic
39
T/F DMARDS can be prescribed forAS
false. DMARDS usually don't work on inflammatory spinal disease. We try to treat AS with NSAIDS and biologics
40
Enteropathic arthritis is often indistinguishable from \_\_\_\_\_\_, usually follows onset of ___ \_\_\_, and has ___ correlation between bowel and joint flares
41
which sex is affected more by reactive arthritis?
male. * follows infectious diarrhea * Salmonella, Yersinia, Shigella, Campylobacter * also associated with urogenital infections * Chlamydia (can be asymptomatic) **• bacteria not identified in most patients**
42
triad in reactive arthritis
1. urethitis 2. conjunctivitis 3. arthritis. reiters triad. plus or minus fever, malaise, fatigue and weightloss and DSCTYLITIS AND ACHILLES ENTHESITIS
43
• 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?
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
note
45
skin characteristics of dermatomyositis
heliotrope rash-- muscle weakness, normal EMG but elevated ESR gottrons rash on PIPs Shawl sign
46
therapy for dermatomyositis
47
sjogrens syndrome symptoms
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
\_\_\_ \_\_\_/ ____ 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.
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
symptoms of limited scleroderma vs diffuse cutaneous systemic sclerosis
• **_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
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
51
scleroderma treatment
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
classification of vasculitis
53
when to expect vasculitis
- 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
specific antibody consisent with SV vasculitis
ANCA
55
lab investigations for GPA
56
note for GPA vasculitis
57
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?
polymyalgia rheumatica. this isn't a vasulitis but it can lead to temporal arteritis or RA.
58
what lab findings are consistent with polymyalgia rheumatica
elevated ESR above 40 - normal muscle enzymes and creatining normal EMG may have ACD no auto-antibodies
59
management of polymyalgia rheumatica
prednisone until ESR is normal - watch for RA appearance after tapering
60
immunologic criteria for lupus
low complement firect coombs test ana anti-DNA Anti-Sm
61
\_\_\_\_ 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 \_\_\_.
**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**.