Osteoarticular V Flashcards

1
Q

events in single espisode connective tissue trauma

A

Healing by scar formation (non functional tissue

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2
Q

Events in chronic repetative connective tissue trauma (3)

A
  • neovascularization
  • increased proteoglycan content
  • impaired mvmt

(not full functionality)

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3
Q

what is a ganglion cyst and how common is it

A

Cystic tumor developing on a tendon aponeurosis

60% of all benign tumors of hand

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4
Q

Gender predominance in connective tissue diseases and which don’t follow

A

Femal morbitiy mainly

-(exeption polyarteritis nodosa, AS)

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5
Q

Main clinical features of polymyositis and dermatomyositis

A

mm weakness, pain, tenderness

  • skin rashes
  • discoloration of upper eyelids
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6
Q

What is neuropathic jt disease also called and what is it characterized by

A

Charcot jt.

-noninflammatory arthritis characterized by progessive jt destruction

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7
Q

what does syringomyelia cause

A

destruction of shoulder or other upper extremity

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8
Q

classic signs of ra

A
  • diarthrodial jts symetrically and bilat
  • early synovial changes (edema and accumulation of plasma cells, lymphocytes and macrophages)
  • juxtaarticular bone loss
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9
Q

Autoimmune findings in RA (3)

A
    • RF factor
  • RF-IgM targeting Fc portion of IgG
  • antinuclear antigen (+ in 30%)
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10
Q

How is the pannus formed in RA

A

inflammatory synovium now contains mast cells, creeps over the surface of the articular cartilage and adjacent structures and is termed pannus

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11
Q

How does the pannus affect the jt in RA

A

Pannus covers the articular cartilage and isolates it from the synovial fluid,
–lymphocytes aggregate and eventually develop follicular centers

=panus eventually erodes articular cartilage/adjacent bone

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12
Q

what causes molecular mimicry with RA

A

EBV

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13
Q

release of immune cells in RA for type IV hypersensitivity

A

Activation of CD4 which release TNF and IL1 (synovial inflammation)

-RF synthesis by b cells in response to synovial antigen

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14
Q

What does RF and IgG and Th17 cause in RA

A

RF and IgG activate complement

IL 17 is released by th17 causing pannus formation (neutropholic infiltration, granulation tissue)

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15
Q

Clinical signs of RA

A

> 6w

  • morning stiff >1hr
  • MCP, PIP jts
  • Ulnar dev (esp. R hand)
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16
Q

How often do Rhematoid nodules aappear in RA and where are they usually located

A

25% of pts

  • ulnar aspect of forearm
  • Viscera (lungsm pericardium, myocardium)
17
Q

When can you see radiographic findins in RA

A

50% of pts show jt space narrowing or erosions in the first 2 years after initial symptoms

18
Q

what are the 3 types of RA

A

1- Self limited= 5-20%

  1. Minimally prog= 5-20%
  2. Progrssive= 60-90%
19
Q

Main characteristics of juvenile RA (age, gnder, associated condition)

A

<16
2:1 F:M

-chronic fever and anemia typical for JRA

20
Q

3 classifications of JRA

A

Polyarticular- 40%, disabling arthritis

Pauciarticular- 4 or fewer jts involved

Still disease- 20%, fever,rash etc

21
Q

Differentiators of JRA vs RA

A
  • less jts involved
  • mc systemic onset
  • more large jts
  • RF and nodules negative
  • ** extra articular manifestations: Pericarditis, myocarditis etc
22
Q

What % of ppl w psoriasis develop psoriatic arthritis

A

10%

23
Q

Symptoms of scleroderma

A
  • raynauds
  • Polyarthritis
  • contraction of skin
24
Q

What is the symptoms of crest syndrome (5)

A
  • calcinosis
  • raynauds
  • esophageal dysmotility
  • sclerodactyly (thickening of skin)
  • teleangioectasia
24
Q

What is the symptoms of crest syndrome (5)

A
  • calcinosis
  • raynauds
  • esophageal dysmotility
  • sclerodactyly (thickening of skin)
  • teleangioectasia