3. Muscular Pathologies Flashcards

1
Q

Muscle Shortening

A

If a muscle is continuously contracted, the actin-myosin filaments remain attached.
• Chronic muscle contracture causes muscle fatigue but also places a strain on the muscles skeletal attachments.

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2
Q

Muscle Strain and Tear

A

Muscle Strain:
• Over-stretching of muscle fibrils or the tendon, occurring when a joint is forced beyond its normal range(“pulled muscle”).
• The muscle remains whole and blood supply intact to permit healing.
• Hamstring and back overstraining injuries are common.
Muscle Tear:
• More significant, where the muscle tears and is no longer whole! More likely to cause bruising.
•Preventing natural complete healing. Can lead to fibrosis.

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3
Q

Impingement Syndrome

A

Impingement syndrome describes a shoulder condition in which movements of the shoulder can be painful and limited.
• In impingement syndrome, the rotator cuff tendons
and/or bursa can become inflamed/damaged. This
is most notable when compressing the space that
they are both found within (the sub-acromial space).
• The sub-acromial space is the area between the
humeral head and the acromion.
• The rotator cuff tendons connect the humerus and
scapula. Normally, when moving the shoulder, the
rotator cuff have to maneuver intricately to prevent
impingement.

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4
Q

Impingement Syndrome: Causes

A

• Overuse & working with the arms raised
overhead.
• More common with increasing age as blood
supply is poor and the tendons degenerate.
• Positional fault –when the head of the humerusdoes not sit perfectly in the socket.
• Bone spurs - can reduce the space available
for the bursa and tendons to move under the
acromion.
• Oddly sized acromion resulting in reduced
space.

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5
Q

Impingement Syndrome: Signs & Symptoms

A
  • Shoulder ache in early stages.
  • Pain when abducting the shoulder or rotating (i.e. Reaching into back pocket)
  • Painful arc of movement.
  • A catching sensation is felt on lowering the arm.
  • Weakness and inability to raise the arm may indicate rotator cuff tear.
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6
Q

Impingemnt Syndrome: Treatment

A

• Cortisone injection, NSAIDs, surgery.

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7
Q

Fibromyalgia

A

Fibromyalgia is a chronic pain disorder, heavily associated with widespread musculoskeletal pain and fatigue.
• Often accompanied by multiple, unexplained symptoms, anxiety, depression and functional impairment of daily activities.
• Women are 10 times more commonly affected that men, mostly occurring aged 30-50.
• Has a neurophysiologic basis, characterised by abnormalities in pain processing by the central nervous system (CNS).
• A form of“central sensitisation”: pain perception to sensory stimulus that would not normally be painful.

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8
Q

Fibromyalgia: Pain Processing

A
  • Fibromyalgia is associated with ‘central sensitisation’ –a central disturbance in pain processing.
  • Normally, sensory input such as light touch & temperature are sent as nerve signals to the brain/spinal cord where it synapses with nerves.
  • In fibromyalgia, alterations occur in pain processing in the spinal cord & brain(‘centrally’).
  • High levels of substance P are found in synapses, which makes nerves more sensitised to pain.
  • Excess postsynaptic nitric oxide production also causes the synapse to amplify pain signals.
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9
Q

Fibromyalgia: Causes & Triggers

A
  • Biological, environmental and possibly genetic factors are thought to contribute:
  • Poor mitochondrial functioning –damaged by free radicals.
  • Altered stress response (i.e. excess cortisol, adrenal fatigue).
  • Post-viral and chronic toxic load e.g. heavy metals, chemicals.
  • Poor gut health –dysbiosis, leaky gut syndrome.
  • Serotonin & noradrenaline deficiencies –play a role in pain tolerance.
  • Sleep dysregulation (fatigue, ↑pain, ↓activity).
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10
Q

Fibromyalgia: Signs & Symptoms

A
  • Widespread (diffuse) musculoskeletal pain.
  • Pain that results from gentle pressure.
  • Feeling of “swollen joints”, often with no actual swelling.
  • Debilitating fatigue & sleep severely disturbed.
  • Headaches (‘muscular’ or ‘migraine’ type).
  • IBS symptoms, numbness, tingling and weakness.
  • Anxiety and depression
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11
Q

Fibromyalgia: Diagnosis

A

Criteria for diagnosis:excess pain on palpation in at least 11 of 18 predefined anatomical points.

  • The patient experiences pain at tender points at a decreased threshold. However:
  • Normal Biopsy.
  • Normal electrical muscle tests.
  • Drug studies show no benefit of NSAIDS but benefits of antidepressants.
  • It is also an ‘exclusion diagnosis’.
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12
Q

Fibromyalgia: Treatments

A

Pain relief
Pain clinics
Anti-depressants
CBT and counselling

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13
Q

Muscular Dystrophy

A

Muscular dystrophies are a group of inherited muscular diseases that cause muscle degeneration and weakness.
Many types of muscular dystrophies exist.
Muscular dystrophies are characterised by:
Progressive skeletal muscle atrophy.
Death of muscle cells & tissue (final stages).
Defects in muscle proteins.

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14
Q

Myasthenia Gravis

A

Myasthenia Gravis is an autoimmune disease of the neuromuscular junction, characterised by fluctuating muscle fatigue & weakness.
• Antibodies block acetylcholine receptors on the motor end plate preventing a nerve impulse being sent to muscle fibres. The muscle becomes progressively weaker.
• Most common in women, age 20-50.
• Muscles of face & neck are commonly affected.

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15
Q

Myasthenia Gravis: Signs and Symptoms

A
  • Weakness of ocular muscles; double vision and ptosis (drooping).
  • Weakness in facial muscles(expressions) which spreads to the proximal limbs.
  • Difficulty with speech, chewing, swallowing.
  • Death may result from failure of the respiratory muscles.
  • Symptoms worsen throughout the day.
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16
Q

Myasthenia Gravis: Treatment

A

• Acetylcholinesterase inhibitors, corticosteroids
to reduce effects of the antibodies (side effects! Including osteoporosis, indigestion, nausea, insomnia, mood changes, diabetes)
• Plasma Exchange in severe cases, injections of
normal immunoglobulins from healthy donors.

17
Q

Duchenne Muscular Dystrophy

A

• Caused by a single gene defect on the X chromosome, affecting males, whilst females
can be carriers. Affects 1 in 3500 males.
• Usually diagnosed 3-5 years of age.
• Associated with a lack of a protein called ‘dystrophin’ in muscle cells. Dystrophin anchors the cytoskeleton to the extracellular matrix.
• If this protein is missing, when the cell contracts
there is no support and the cell membrane becomes leaky, allowing materials to flood in.
• This results in muscle degeneration and necrosis

18
Q

Duchenne Muscular Dystrophy: Signs and Symptoms

A
  • Delayed walking.
  • Difficulty getting up from sitting or lying position.
  • Clumsiness, frequent falls.
  • Waddling gait.
  • Speech delay.
  • Gowers sign. (using hands to push on legs to stand)
19
Q

Duchenne Muscular Dystrophy: Diagnosis

A
  • Serum creatine kinase(10-100x normal). This is also often raised in carriers.
  • Genetic analysis and muscle biopsy.
20
Q

Duchenne Muscular Dystrophy: Prognosis

A
  • All muscle types affected: skeletal, smooth and cardiac.
  • Small amounts of dystrophin also present in nerve cells (IQ is affected).
  • Prognosis poor: usually wheelchair support needed by 10 years and ventilation by 20 years.
  • Most die in their late twenties, often from pneumonia and cardio-respiratory failure.
  • Therapeutic strategies aimed at prolonging independent