module 9 disorders of skeletal muscles, peds, aging Flashcards

1
Q

contracture

A

muscle fiber shortening without an action potential

- cause by failure of the sarcoplasmic reticulum (calcium pump) even with available ATP; lack of use

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2
Q

stress induced muscle tension

A
neck stiffness
back pain
clenching teeth
hand grip 
headache
-associated with chronic anxiety 
- work demands
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3
Q

fibromyalgia

A
muscle pain 
target points
- occiput
- trapezius
- suprasinatus
- gluteal
- greater trochanter
- anterior neck
- second rib
- lateral epicondyle 
- knee 
fatigue 
sleep disturbance
increased stimulus to touch
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4
Q

disuse atrophy

A

reduction in normal size of muscle cells due to prolonged inactivity

  • bed rest
  • trauma
  • casting
  • nerve damage
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5
Q

disuse atrophy tx

A

isometric movement ans passive lengthening exercises

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6
Q

diseases of energy metabolism

A
McArdle disease
- myophysphorylase dificiency
Acid Maltase deficiency 
- Pompe disease
Myoadenylate deaminase deficiency (MDD)
Lipid Deficiencies
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7
Q

Inflammatory muscle disease (dermatomyositis, polymyositis)

A

Focal or extensive degeneration fo muscle fibers attributable to inflammation infiltrates of lymphocytes, macrophages
- inflammatory cytokines, autoantibodies, cytotoxic
-> necrosis of muscle fibers -> fatty replacement -> weakness
collectively: myositis
viral, bacterial, and parasitic myositis
- staphylococcus aureus
- trichinosis
- toxoplasmosis

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8
Q

inflammatory muscle disease (myositis) s/s

A

weakness in proximal limb muscles

esophageal dysmotility can be seen

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9
Q

dermatomyositis

A

gottron papules: flat top over dorsal surface of hand joints
scaly patches over joints
rashes

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10
Q

Duchenne Muscular Dystrophy

A

most common muscular dystrophy
X-linked recessive inheritance: Mostly males affected
- deletion of segment of DNA on short arm of the X
Duchene muscular dystrophy gene
- encodes for dystrophin protein (deficient)
– mediates the anchorage of the actin cytoskeleton of the skeletal muscle fiber to the basement membrane -> wasting of skeletal muscle

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11
Q

Duchenne muscular dystrophy s/s

A

shoulders and arms held back when walking
sway back
weak butt muscles
knees bend to take wt
thick lower leg muscles (mostly fat, not strong)
tight heel cord -> toe walking
weak muscles in front of leg -> foot drop
belly sticks out due to weak abd. muscles
thin weak thighs
poor balance -> falls often, clumsy
decreased dystrophin -> weakened cell membrane -> extracellular fluid leaks into cell -> muscle fiber necrosis

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12
Q

Dechenne muscular dystrophy tx

A

education
preservation of physical function as long as possible
prevent contractures

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13
Q

genu varum

A

bowleg
peaks at 2.5 years
occurs in all newborns due to intrauterine stress
pathogenic past 2.5 years

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14
Q

genu valgum

A

knock-knees
peaks at 5-6 years
pathologic past 5-6 years

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15
Q

congenital defects

A
syndactyly: webbing or fusion of fingers
vestigial tabs: extra digits 
deformities of foot: 
- metatarsus adductus (forefoot adduction ) 
- equinovarus deformity (club foot)
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16
Q

developmental dysplasia of the hip

A

abnormality of the proximal femur, acetabulum, or both
risk factors (head of femur in pelvis)
- female, metatarsus addutus, torticollis, oligohydramnios, 1st pregnancy, breech

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17
Q

osteogenesis imperfecta

A
brittle bone disease 
defect in collagen production 
- bone and vessel collagen 
results in osteoporosis, bowed and deformed limbs, short stature, spine curvature, and bluish sclera
can be evident in utero; fractures
18
Q

Juvenile Rheumatoid arthritis

A
3 forms of onset
- pauciarticular: < 3 joints
- polyarthritis: > 5 joints
- systemic disease: most common
Predominantly large joints
subluxation and ankylosis of spine 
joint pain not as severe as adult
chronic uveitis 
lab tests: detect inc. ANA, seldom detect rheumatoid factor 
*RA nodes not limited to subcutaneous- can be found in the heart, lungs, eyes, and other organs
19
Q

Ricketts

A

osteomalacia of peds
softening of bones due to defective mineralization
cartilage in growing epiphysis fails to calcify
- not replaced by bone and continue to enlarge -> widening and irregularities
- delayed eruption of teeth
- decreased muscle tone

20
Q

Osteochondrosis

A

Legg-Calve-Perthes disease

Osgood-Schlatter disease

21
Q

Legg-Calve-Perthes disease

A

interrupted blood supply to the femoral head
self-limiting disease
deformation due to ischemia is permanent

22
Q

Osgood-Schlatter diesase

A

tendinitis of the anterior patellar tendon and osteochondrosis of the tubercle of the tibia
- tendon does not grow as quickly as bone does

23
Q

osteoarthritis (degenerative joint disease)

A

progressive loss of articular cartilage and formation of thick subchondral bone and new bone at joint margins

  • seen more with increased age: >70
  • related to wear and tear
  • breakdown of proteoglycan and collagen -> decrease hydration of cartilage -> increased wear damage
24
Q

osteoarthritis s/s

A
enlarged joints
crepitus
am stiffness for 30 minutes
pain with function 
localized
deformity
unilateral
25
Q

rheumatoid arthritis

A
type III hypersensitivity 
inflammatory joint disease
systemic autoimmune damage to connective tissue, primarily in joints (synovial membrane) 
Women > men
peak 40's-50's 
> risk with family hx
26
Q

rheumatoid arthritis s/s

A
bilateral, symetrical
malaise
fatigue 
diffuse pain 
\+ for RF 
red and warm
27
Q

ankylosing spondylitis

A

inflammatory joint disease of the spine or sacroiliac joints causing stiffening and fusion of the joints
systemic, immune inflammatory disease
Primary site: enthesis
- where ligament, tendons, and the joint capsule are inserted into bone
cause unknown but associated with HLA-B27 antigen (genetic component)

28
Q

ankylosing apondylitis s/s

A

low back pain: improves with exercise, not relieved with rest
morning stiffness
loss of lumbar lordosis
- hips and knees compensate -> lower joint degradation/deformity
- restricted postural position -> decreased chest expansion

29
Q

Gout

A

metabolic disorder that disrupts the body’s control of uric acid production or excretion
- high levels of uric acid
uric acid levels high enough to crystallize
- crystals deposit in connective tissues throughout the body.

30
Q

gout risk factors

A
increase with age
diet (increased purine)
chronic kidney disease
family Hx
soda/ carbination 
increased ETOH
31
Q

gout s/s

A
recurrent episodes 
accumulation of tophi (crystals)
impaired renal system 
inflammation, pain 
attacks subside in 1-2 days but may last 1-2 weeks
32
Q

4 phases of gout

A
  • asymptomatic hyperuricemia
  • acute gouty arthritis
  • intercritical gout (betwen attacks)
  • chronic tophaceous gout ( after 10 or so years tophi appear)
33
Q

Primary and secondary skin lesions

A

primary: original appearance
secondary: appearance modified by normal progress over time

34
Q

skin lesion features

A

size
symmetry of color and shape
distribution

35
Q

skin lesion patterns

A
symetric
sun-exposed
genital
intertriginous (warm, moist skin)
acral (extremities, ears, nose)
36
Q

primary lesions

A
macule
papule
nodule
tumor
plaque
wheal
vesicle
bulla
pustule
37
Q

secondary lesions

A
erosion
ulcer
fissure
atrophy
excoriation
crust
scale
lichenification
scar
keloid
38
Q

childhood skin disorders

A
lacerations
burn
head lice
scarlet fever
tinea capitis
impentigo
rubella, roseola, rubeola (measles)
chicken pox
39
Q

Teen skin disorders

A

acne

exacerbated chronic skin disorders

40
Q

geriatric skin disorders

A
keratoses
skin cancer
fungal infections
dematitis
asteatoses (scaling)
nevi (moles) 
lentigines (liver spots)
pigmentary disorders
psoriasis
urticaria
comedones (black heads)
cherry angiomas
skin tags 
senile purpura