muscle pathology Flashcards

1
Q

explain how muscle contraction occurs (action potential stimulation)

A
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2
Q

what is myaesthenia gravis + causes

A

Myasthenia gravis is a rare long-term condition that causes muscle weakness.

It most commonly affects the muscles that control the eyes and eyelids, facial expressions, chewing, swallowing and speaking.

  • caused by antibodies to the nicotinic acetyl choline receptor at neuromuscular junction
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3
Q

what 3 blood tests might be done for a person with myasthenia gravis

A
  1. anti-acetyl choline receptor antibodies
  2. anti-Musk
  3. anti-LRP4
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4
Q

what do anti-acetyl choline receptor antibodies, anti-Musk, anti-LRP4 all have in common

A

all muscle directed anti-bodies

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5
Q

what are 3 potential treatments for myasthenia gravis

A
  • acetyl choline esterase inhibitors (overloads remaining functional acetyl choline receptors)
  • immunosuppressive treatment can treat underlying pathology
  • surgical treatment of thymectomy (removal of thymus) can have therapeutic effect
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6
Q

what is thyoma

A

rare type of cancer arising in epithelial tissue of the thymus

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7
Q

what percentage of patients with thyoma will also have myasthenia gravis and hence what can be done to help reduce progression of myasthenia

A

30-40%

removal of thymoma can improve myasthenic disease progression

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8
Q

what is Lambert-eaton myasthenic syndrom

A

similar to myasthenic gravis

It is a miscommunication between the nerve cell and the muscles that lead to the gradual onset of muscle weakness.

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9
Q

what is a radiological significance with lamber-eaton

A

it is associated with paraneoplastic syndrome which means its a rare disorder that occur when the immune system has a reaction to a cancerous tumor known as a “neoplasm.”

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10
Q

why type of cancer is Lambert-eaton associate with typically

A

small cell lung cancer

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11
Q

what are the 3 components of the anaesthetic triad (general anaesthesia)

A

hypnosis

muscle relaxation

analgesia

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12
Q

what is duchene muscular dystrophy + cause

A

x-linked generic disorder that presents in childhood with weakness around pelvis

unlikely to live past 30 and are wheelchair bound

  • caused by deficiency in dystrophin which links actin skeleton to extracellular matrix

(Lack of the dystrophin protein in muscle cells causes them to be fragile and easily damaged as gene on x-chromosome mutated)

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13
Q

what is facioscapulohumeral muscular dystrophy

A

genetic myopathy caused by excess expression of the DUX4 protein

affects muscle of face and shoulder girdle (clavicle and scapula providing bony link to arm and trunk)

winged scapula may be treated with surgery

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14
Q

what is steroid induced myopathy

A

corticosteroid ( reduce inflammation/overactive immune response) when taken long term can cause muscle atrophy (due to poor protein synthesis in muscles)

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15
Q

what are the type of muscle that steroid induced myopathy affects

A

high usage muscles e.g thigh

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16
Q

what is rhabdomyolysis

A

damaged muscle tissue releases its proteins and electrolytes into the blood/ damaged skeletal muscle breaks down rapidly

17
Q

what can rhabdomyolysis be caused by

A

prolonged compression of muscle

extreme muscle exertion

certain medication (psychiatric-neuroleptic malignant syndrome)

18
Q

what 3 things do the muscles in rhabdomyolysis release and why are they bad?

A

myoglobin- can lead to kidney damage and subsequent kidney failure

potassium- difficult for body to remove in during kidney failure and high levels can cause cardiac arrest

creatine kinase- not bad but used as check in blood test to see if damage has occured

19
Q

what is statin induced myopathy

A

can cause muscle cramps (that subside with discontinuation of drug)

20
Q

what is a good indicator in blood samples to show that there is statin induced myopathy

A

high levels of creatine kinase

21
Q
A