muscle disorders Flashcards

1
Q

major signs of muscle disorders

A

muscle stiffness - tying up
weakness, staggering, muscle atrophy, muscle fasiculations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

describe rhabdomyolysis

A

rapid degeneration of muscle cells due to excessive calcium accumulation in muscle cells.

produces free radicals, proteases, and cytokines.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the difference between myogenic atrophy and neurogenic atrophy

A

myogenic- type two. m cell destruction

neurogenic- type 1and 2. denervation. very rapid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is a common clinical sign with HYPP

A

muscle fasiculation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is hypp

A

-hyperkalemic periodic paralysis– from ion channel defects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is the biggest differential for muscle disease

A

exercise associated or not

weakness vs pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

if there is muscle pain associated with poor performance what are we thinking

A

tying up. need to check CK

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what causes muscle weakness poor performance

A

neurogenic or myogenic atrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the three exercise related diseases and how do they present differently

A

sporadic rhabdo-occurs randomly, inc CK

chronic rhabdo- repeat incidences, inc CK

chronic myopathy- NORMAL CK, repeat stiffness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

nonexertional myopathies

A

metabolic, inflammatory, toxic, trauma, infection, nutritional, muscle atrophy, fasciculations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what are the key things we look at in our PE for muscular disease

A

muscle mass, symmetry, behavior, palpation for pain, tone, swelling

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what does CK and AST tell us about whats going on

A

CK short acting. will tell us if the injury is acute or ongoing

AST will tell us the chronicity longterm. takes weeks to return to normal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

when does CK return to normal

A

48 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what number CK are we worried about muscle damage

A

> 4000

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how do we confirm rhabdomyolysis

A

CK ex response. preex
moderate exercise (not severe)
and looking for a 3x increase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what should we remember about rhabdomyolysis systemically

A

myoglobin excreted in the urine.

myoglobinuria causes renal tubular necrosis

17
Q

what is the most diagnostic tool

A

muscle biopsy

18
Q

when does a muscle biopsy not yield results

A

HYPP/fasciculations

19
Q

what is PSSM

A

polysaccharide storage myopathy.
T1 and T2
high [] glycogen in the muscles.

20
Q

difference between PSSM T1 and T2

A

T1 has gsy1 gene

21
Q

treatment for PSSM

A

stall rest, then consistent exercise, decrease starch content

22
Q

general recommendation treatment for all these diseases

A

consistent exercise