Exam 5: Musculoskeletal Pathologies Flashcards

1
Q

osteoarthritis

A
  • older ppl or athletes
  • breakdown of articular cartilage
  • exacerbated by use
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2
Q

RA

A
  • autoimmune
  • small joints
  • joints warm / painful / stiff w/ inactivity
  • symmetric

ulnar deviation of metacarpophalangeal joints

HANDS

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3
Q

RA - histologically

A

synovium thickened, hyperplastic, lots of lymphoid aggregates

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4
Q

gout

A

excessive uric acid

BIG TOE with TOPHI

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5
Q

gout risk factors

A
age
duration of hyperuricemia
heavy ALCOHOL
obesity
drugs (thiazides)
lead toxicity
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6
Q

tophi

A
  • urate crystals with inflammation

- NEEDLE LIKE

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7
Q

pseudogout

A
  • calcium phosphate
  • hereditary
  • RHOMBOID / GEOMETRIC crystals
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8
Q

bacteria that can cause infectious arthritis

A
  • TB
  • lyme: borrelia burgdorferi
  • gonococcus
  • staph aureus
  • influenza
  • salmonella
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9
Q

viruses that can cause infectious arthritis

A

parvovirus
rubella
HCV

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10
Q

what kind of patients are associated with salmonella?

A

sickle cell patients

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11
Q

type 1 muscle fiber

A
  • slow twitch
  • weight bearing
  • mitochondrial / ox phos pathway
  • lipid metabolism
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12
Q

type 2 muscle fiber

A
  • fast twitch
  • purposeful movement
  • glycogen metabolism
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13
Q

denervation atrophy - histologically

A
  • angular, atrophic
  • mm shrinks, nuclei remain on outside and look like giant cells
  • target fibers
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14
Q

type grouping

A
  • after denervation, the nerve closest to the muscles re-enervates them
  • it’s when you see ONE type of mm fibers - lack of checkerboard pattern
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15
Q

amylotrophic lateral sclerosis

A
  • 60 years old, M>F
  • muscular atrophy
  • hand weakness (early)
  • progressive + respiratory mm weakness (late)
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16
Q

ALS death due to

A

respiratory failure

bronchopneumonia

17
Q

ALS macroscopic findings

A
  • shrunken / atrophic anterior nerve roots

- distal > proximal

18
Q

ALS microscopic findings

A
  • bunina inclusion bodies

- degeneration of myelinated fibers in the corticospinal tracts

19
Q

a denervation injury always looks like this histologically

A

angulated, atrophic fibers

20
Q

a myopathy always looks like this histologically

A
  • rounded atrophic fibers
  • vacuoles
  • degeneration, regeneration, fibrosis
21
Q

2 mutations of dystrophin gene

A

Duchenne MD,

Becker MD

22
Q

duchenne MD

A
  • dystrophinopathy
  • dystrophin ABSENT
  • no brown
23
Q

becker MD

A

dystrophine reduced

- some brown

24
Q

dystrophinopathies - clinically

A
  • proximal weakness
  • calf pseudo-hypertrophy
  • CK elevated early
  • death from respiratory, cardiac failure
25
Q

polymyositis

A
  • an inflammatory myopathy
  • infiltrate can be aggressive
  • becomes necrotic post infiltration
26
Q

dermatomyositis

A
  • facial rash

- perifascicular atrophy

27
Q

McArdle’s Disease

A
  • glycogen defect
  • myophosphorylase deficiency
  • PAS stain +
28
Q

Carnitine Palmityl Transferase Deficiency

A
  • lipid defect

- Oil red O stains red

29
Q

mitochondrial myopathies

A
  • proximal weakness

- opthalmoplegia

30
Q

drug induced myopathies can be caused by

A
  • steroids
  • statin drugs
  • colchicine
  • ethanol
31
Q

malignant hyperthermia

A
  • an ion channel myopathy
  • hypermetabolic state
  • trigger: ANESTHESIA
  • gene mutation in Ca channel (RYR1)
32
Q

Myasthenia gravis

A
  • loss of Ach receptors
  • post synaptic
  • thymus problems
  • worsened by exercise
  • ptosis
33
Q

Lambert Eaton Syndrome

A
  • ppl with small cell lung cancer
  • presynaptic
  • Ab to presynaptic voltage gated Ca channels