Pankratz DSA: MSK Joint Pathology Flashcards

1
Q

Osteoarthritis

A
  • Herbeden nodes
  • Bouchard nodes
  • Osteophytes
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2
Q

ORheumatoid arthritis

A
  • rheumatoid factor
  • rheumatoid nodules
  • pannus
  • swan-neck deformity
  • boutoneeire’s deformity
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3
Q

Osteoarthritis

A
  • degeneration of cartilage that results in structural and functional failure of synovial joints
  • chondrocyte injury
  • weight bearing joints
  • asymmetric
  • loss of knee cartilage medially
  • trauma
  • joint space narrowing
  • Herbeden nodes and Bouchard nodes
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4
Q

Herbeden node

A

-in DIP joint

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5
Q

Bouchard node

A

-in PIP joint

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6
Q

Rheumatoid arthritis

A
  • autoimmune
  • CD4 T cells
  • HLA-DRB1 allele
  • PTPN22 gene
  • improves with use
  • symmetric
  • systemic symptoms
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7
Q

What are the long-term complications for RA?

A
  • systemic amyloidosis
  • Caplan syndrome
  • Anemia of chronic disease
  • Felty syndrome
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8
Q

Clinical findings for RA

A
  • pannus
  • fibrinoid necrosis with palisaing histiocytes
  • radial deviation or wrist, ulnar deviation of fingers
  • swan neck deformity
  • boutonneire defomty (opp of swan)
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9
Q

What was the bolded thing under RA that wasn’t rheumatoid factor?

A

-Antibodies against citrullinated peptides

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10
Q

What is Rheumatoid factor?

A

-serum IgM or IgA autoantibodies that bind to Fc portion of their own IgG

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11
Q

Juvenile idiopathic arthritis

A
  • arthritis b4 age of 16 and persists for at least 6 weeks
  • more common in large joints
  • absent rf and rheumatoid nodules
  • positive ANA
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12
Q

Seronefative spondyloarthropathies

A
  • immune mediated disease triggered by T-cell response to unidentified antigen
  • Ankylosing spondylitis
  • reactive arthritis
  • enteritis associated arthritis
  • psoriatic arthritis
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13
Q

Immune mediated disease triggered by t cell response to unidentified antigen

A
  • pathologic change in ligamentous attachments not synovium
  • involvement of SI joints
  • Absence of RF
  • HLA-B27 association
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14
Q

Ankylosing spondylitis

A
  • destrution of articular cartilage and bony ankylosis
  • SI and pophyseal joints
  • 20-30’s
  • low back pain with spinal immobility
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15
Q

Reactive arthritis

A
  • Arthritis and non-gonoccocal urethritis or cervicitis and conjunctivitis
  • HLA-B27
  • Autoimmune rxn initiated by prior infection
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16
Q

clinical manifestations of reactive arthritis

A
  • develops within weeks of urethritis or diarrhea
  • asymmetric pattern involving knees, ankles, feet
  • may wax and wane for weeks to 6 months
17
Q

Enteritis associated arthitis

A
  • cause by: yersinia, salmonella, shifella, camplyobacter
  • lipopolysaccharides stimulate immunological response
  • abrupt onset involving usually involving knees and ankles
  • typically lasts about 1 year then resolves
18
Q

Psoriatic arthritis

A
  • chronic arthropathy that affects peripheral and axial joints and enthuses
  • HLA-B27
  • 30-50
  • predominantly in hands and feet
  • Asymmetric pattern that usually first involves DIPJ
  • clinical findings: PENCIL IN A CUP DEFORMITY
19
Q

What are the kinds of infectious arthritis

A
  • Suppurative arthritis
  • Mycobacterial arthritis
  • Lyme arthritis
  • Viral arthritis
20
Q

Suppurative arthritis

A
  • bacterial infection enters joint through hematological spread
  • non gono…. single joint
  • drug users: axial joints
  • joint aspiration shows purulent fluid with ID of causal agent
  • sudden onset fever, leukocytosis, elevated ESR
  • painful swollen joints
21
Q

most common causal agent for Children suppurative arthritis

A

-H influenza: gram negative coccobacillus

22
Q

Adult suppurative arthritis

A

-S. Aureus: gram + cocci

23
Q

Suppurative arthritis from sickle cell disease

A

-salmonella: gram - rod

24
Q

suppurative arthritis from sexually active individuals

A

-N. gonorrhea: gram negative diplococcus

25
Q

Mycobacterial arthritis

A
  • M tuberculosis
  • complication of osteomyelitis or hematogenous dissemination from a visceral (most commonly pulmonary)
  • gradual progressive pain in weight bearing joints
  • confluent granulomas with central caseous necrosis
26
Q

Lyme arthritis

A
  • Borrelia burgdorferi: spirochete
  • Late stage; untreated individuals
  • large joints
  • diagnosis made by ID of spirochete and anti borrelia antibodies
27
Q

Gout

A
  • hyperuricemia
  • synovium, neutrophilic infiltrate, edematous
  • needle shaped negative birefringence
28
Q

What is Tophaceous gout?

A
  • 12 yrs after initial acute attack
  • synovium: hyperplastic, fibrotic, thickened, which leads to pannus formation and bone erosions
  • development of tophi
29
Q

What are tophi

A

large aggregations of urate crystals surrounded by inflammatory rxn of foreign body giant cells

30
Q

Complications (gouty nephropathy)

A
  • uric acid nephrolithiasis

- pyelonephritis

31
Q

What does radiology look like in gout?

A

-justa-articular bone erosion caused by osteoclastic bone resorption and loss of joint space

32
Q

Calcium pyrophosphate deposition disease (pseudo-gout; chondrocalcinosis)

A
  • articular cartilage proteglycans, which normally inhibiti mineralizatio, are degraded allowing crystallization around chondrocytes
  • > 50 yo
  • usually asymptomatic
  • knees, wrists, elbows, shoulders, ankles
  • rhomboid crystals
  • postivie birefringence
  • management: supportive
33
Q

hereditary psuedogout

A
  • auto dominant; germline mutation in pyrophosphate channel

- delvelopment of crystals at an early age with severe steoarthritis

34
Q

-secondary pseudogout

A

-associated with previous joint damage, hyperparathyroidism, hemochromatosis, hypomagnesemia, hypothyroidism, ochronosis, diabetes