Weakness Flashcards

1
Q

what is the upper motor neuron pathway

A

cortex > subcortical tracts > internal capsule > brainstem (decussation in pyramids) > spinal cord > anterior horns

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2
Q

what is the lower motor neuron pathway

A

follows directly on from upper mn
ventral roots > plexi > peripheral nerves > neuromuscular junction > muscle

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3
Q

what is pyramidal weakness

A

in upper motor neuron lesions unless paralysis is complete (plegia) a specific pattern is seen
in upper limbs, extensors are weaker than flexors
in lower limbs, flexors are weaker than extensors

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4
Q

what does the suffix paresis mean

A

mild-moderate weakness

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5
Q

what does the suffix plegia mean

A

more severe weakness

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6
Q

how are weakness patterns catergorised

A

according to the limb affected
mono - single limb (arm or leg)n
para - both legs
tetra - all four limbs (quadra is also used)
hemi - affecting arm and leg on one side

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7
Q

what is the cortex

A

descending motor pathways begins here in the primary motor cortex
organised by body regions
large areas devoted to tongue, face and hand
lower limb is given a relatively smaller region on medial surface
lesions will selectively affect certain regions

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8
Q

difference between cortical and diffuse lesiosns

A

cortical lesions only affect a selected region
diffuse lesions (major infarction) will affect a large area

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9
Q

how do lesions in other upper motor neurons affect the body

A

lesions outwith the cortex affect broader territory
this is due to tracts travelling closely together

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10
Q

what other clues are there to cortical lesions

A

seizures
other cortical deficits such as aphasia

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11
Q

how do lesions in the corona radiata and capsule affect the body

A

lesions here affect broad anatomical territory (eg hemiparesis)

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12
Q

what is the key to localisation of brainstem lesions

A

corticospinal tract decussates at the pyramids in the medulla
cranial nerves emerging from the brainstem tend to travel on the same side they emerge from
this leads to crossed signs - ipsilateral cranial nerve lesion contralateral signs in limbs
often lesions are very focal

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13
Q

describe a cervical cord lesions

A

lesions affecting bilateral cord will produce tetraparesis/plegia
spasticity and brisk reflexes will be present, with upgoing plantars (Babinski reflex)
other markers may be sensory loss and a disturbance to bowel and bladder

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14
Q

describe thoracic cord lesions

A

will only produce weakness in lower limbs
spastic tone, pyramidal weakness, brisk reflexes upgoing plantars
sensory disturbance
sphincter disturbance

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15
Q

what is different about the cauda equina compared to the rest of the spinal cord

A

nerve roots descend before exiting via the foramina
these roots also carry autonomic and sensory fibres

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16
Q

what can lesions in the cauda equina cause

A

bilateral paralysis
sensory loss
LMN signs (eg areflexia)
loss of bladder/bowel function
cauda equina syndrome is an emergency, threat of permanent paralysis

17
Q

what is radiculopathy

A

compression of nerves where they exit the spinal canal

18
Q

what are the causes of radiculopathy

A

prolapsed intervertebral disc
facet joint hypertrophy
spondylolisthesis
radiculitis (inflammation)

19
Q

symptoms of radiculopathy

A

pain which radiates down the nerve (radicular pain) dermatomal sensory loss with or without weakness in the site (LMN signs on exam)
examination may elicit characteristic pain via provocative manoeuvres, loss of reflexes in affected territory

20
Q

what are plexi and how does a lesion impact them

A

plexi are where spinal nerves combine and individual nerves emerge
lesions here produce a pattern of weakness not conforming to an individual root territory, nor peripheral nerve

21
Q

impact of peripheral nerve lesions

A

lesions here affect individual nerves (mononeuropathy)
signs will reflect loss of function in the region supplied by the specific nerve
usually sensory, can be with or without motor features
some nerves are sensory or motor only

22
Q

how do peripheral nerve lesions occur

A

nerves are damaged
can be due to a variety of processes such as compression, tumours or inflammation

23
Q

describe polyneuropathy

A

multiple nerves affected in multiple limbs (+/- cranial nerves)
various patterns exist but in general longest nerves are damaged first (‘glove and stocking’ sensory loss, distal weakness)
reflexes are diminished or absent
chronically will see wasting, sometimes fasciculations

24
Q

what is the neuromuscular junction

A

synapse between motor neuron and muscle

25
Q

what does issues with the NMJ appear as

A

fatigable weakness (sustained exertion on bedside testing causes decreasing power)
usual pattern is weakness affecting proximal muscles, ocular muscles, bulbar muscles, neck muscles
sensation is normal and reflexes are unaffected

26
Q

what is myasthenia gravis

A

autoimmune disorder where there are antibodies to acetylcholine receptor on muscle

27
Q

what is the treatment for myasthenia gravis

A

pyridostigmine (acetylcholinesterase)
immunosuoression
supportive measures
in some cases surgery
avoid drugs which may worsen the disorder

28
Q

what is muscle myopathy

A

when many different diseases exist affecting muscles
many different patterns exist
general pattern of proximal weakness, fatigability is not seen, reflexes are generally preserved, sensation is normal
other features include characteristic regions of atrophy (or hypertrophy), contractures, pain, dysmorphic features

29
Q

what is polymyositis

A

autoimmune disorder causing muscle inflammation
may be associated with underlying cancer

30
Q

what is the treatment for polymyositis

A

immunosuppression
supportive measures
screen for underlying cancer and treat if present