SKELETAL MUSCLE PATHOLOGY Flashcards

(34 cards)

1
Q

what are the characteristics of muscular dystrophies

A

muscle fiber necrosis and regeneration

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2
Q

what is Duchenne muscular dystrophy?

A

X-linked, loss of function mutation of a structural protein call dystrophin

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3
Q

what is the most common muscular dystrophy

A

Duchenne Muscular Dystrophy

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4
Q

Dystrophin is a key component of the

A

dystrophin glycoprotein complex

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5
Q

the dystrophin glycoprotein complex provides

A

mechanical stability to the muscle fiber and it’s cell membrane during muscle contraction

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6
Q

defects in the dystrophin glycoprotein complex can lead to what?

A

sarcolemma tears: calcium influx from ECF -> ultimately triggering muscle fiber necrosis

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7
Q

for Duchenne muscular dystrophy, weakness begins in ? and extends to ?

A

pelvic girdle muscles
shoulder girdle

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8
Q

what is a test for Duchenne muscular dystrophy?

A

Gower’s sign

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9
Q

For Duchenne muscular dystrophy patients, what is remarkedly elevated in first decade of life then decreases as diseases progresses

A

creatine kinase

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10
Q

what is generally similar but less severe than Duchenne Muscular dystrophy and has slower progression

A

Becker Muscular Dystrophy

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11
Q

what is becker muscular dystrophy?

A

X-linked mutation in dystrophin which results in truncated dystrophin protein that retains partial function

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12
Q

what is myotonia?

A

sustained involuntary muscle contractions

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13
Q

what is myotonic dystrophy?

A

autosomal dominant disorder caused by expanision of triplet repeats

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14
Q

what are the two types of myotonic dystrophy

A

type I and II

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15
Q

what is type I myotonic dystrophy?

A

expansion of CGT trinucleotide repeat within the myotonic dystrophy protein kinase (DMPK) gene

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16
Q

what is type II myotonic dystrophy?

A

CCTG repeat expansion within the gene nucleic acid-binding protein (CNBP) gene

17
Q

what is the most common drug-related myopathy?

A

statin myopathy

18
Q

myopathy is thought to result from?

A
  • Decreased cholesterol concentrations may impact sarcolemma
  • Depletion of Coq10 (Ubiquinone)
19
Q

what is myasthenia Gravis?

A

Autoimmune condition associated with autoantibodies directed against acetylcholine receptors

20
Q

what is a tumour of thymic epithelial cells

21
Q

what are common initial findings of myasthenia gravis?

A

ptosis and diplopia

22
Q

what is a red flag for myasthenia gravis?

A

Myasthenic crisis

23
Q

what is the first line of treatment for myasthenic crisis?

A

acetylcholinesterase inhibitors

24
Q

what are two common types of skeletal muscle tumours

A

rhabdomyosarcoma and synovial cell sarcoma

25
what is the most common soft tissue sarcoma of childhood?
alveolar and embryonal rhabdoomyosarcoma
26
what are the 4 subtypes of rhabdomyosarcoma
Alveolar, Embryonal, Pleomorphic, Spindle cell/sclerosis
27
what is rhabdomyosarcoma?
malignant mesenchymal tumour with skeletal muscle differentiation
28
what is the malignant cell of rhabdomyosarcoma?
rhabodomyoblast
29
what are rhabodomyoblast rich in
myosin and actin filaments
30
what is the most common soft tissue tumour in adolescents and young adults?
synovial cell sarcoma
31
what is fibromyalgia?
Syndrome of persistent widespread pain, stiffness, fatigue, disrupted sleep, and cognitive difficulties. It is often accompanied by anxiety/depression and impairment of activities of daily living.
32
what is used to diagnose fibromyalgia?
widespread pain index - score of 0-19 AND Self-adminstered patient questionnaire - score of 0-12
33
what is chronic fatigue syndrome
Characterized by unexplained and profound fatigue that is worsened by exertion - Accompanied by cognitive dysfunction and impairment of daily functioning that persists for at least 6 months
34
what is another name of chronic fatigue syndrom
Myalgic encephalomyelitis