Localizing the lesion Flashcards

1
Q

Describe the corticospinal tracts

A

Carry motor information from the precentral gyrus of the frontal cortex up to synapse with anterior horn cells in the spinal cord

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2
Q

Describe the pattern of weakness in an UMN lesion

A

Pyramidal pattern
Arm - extensors are weaker
Leg - flexors are weaker

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3
Q

Where does spasticity develop in an UMN lesion

A

Spasticity occurs in the stronger muscle groups (arm - flexors, leg - extensors)

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4
Q

How does spasticity manifest?

A

Increased tone that is velocity dependent (The faster you move patients muscles, greater the resistance till it suddenly gives way like a clasp knife)

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5
Q

Does muscle wasting occur with an UMN lesion?

A

No - disuse atrophy however may occur

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6
Q

Describe the reflexes in an UMN lesion

A

Hyperreflexia
Positive Babinski sign - upgoing plantars
Clonus (elicited by rapidly dorsiflexing the foot, <3 rhythmic downward jerks of the foot are normal)

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7
Q

What can UMN mimic in the first few hours?

A

LMN

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8
Q

Where is the damage in an UMN lesion

A

Anywhere in the corticospinal tract

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9
Q

Where is the damage in a LMN lesion

A

Anywhere from the anterior horn cells distally, including nerve roots, plexuses and peripheral nerves

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10
Q

What does the pattern of weakness in a LMN lesion correspond with?

A

The muscles supplied by the involved neurons

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11
Q

Describe the tone in muscles when a LMN lesion is present?

A

Hypotonia/flaccidity - the limb feels soft and floppy, providing little resistance to passive stretch

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12
Q

Describe the signs present in the muscles in LMN lesions

A

Wasting and fasciculations

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13
Q

What are fasciculations

A

spontaneous involuntary twitching

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14
Q

Describe the reflexes in a LMN lesion

A

Hyporeflexia (reduced/absent)

Plantars remain flexor

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15
Q

What is the main differential of a LMN lesion

A

Primary muscle disease

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16
Q

How do you distinguish between primary muscle disease and a LMN lesion

A

In LMN lesion - symmetrical loss, reflexes reduced/absent and there is no sensory component

17
Q

List some conditions which may present with mixed UMN and LMN signs

A

MND
B12 deficiency
Taboparesis

18
Q

How do pain and temperature sensations travel?

A

Along small fibres in peripheral nerves and the anterolateral (spinothalamic) tracts in the cord and brainstem

19
Q

How does joint position and vibration sense travel?

A

In large fibres in peripheral nerves and the large dorsal columns of the cord

20
Q

Which classification chart is used to grade power?

A

MRC classificaiton

21
Q

Describe the MRC classification

A

Grade 0 - No muscle contraction
Grade 1 - Flicker of contraction
Grade 2 - Some active movement
Grade 3 - Active movement against gravity
Grade 4 - Active movement against resistance
Grade 5 - Normal power (allow for age)

22
Q

Where would the lesion be in a cranial nerve palsy contralateral to a hemiplegia?

A

Brainstem injury on the side of the cranial nerve palsy

23
Q

Describe the signs of a cord lesion

A

LMN signs at the level of the lesion
UMN signs below the level of the lesion
Sensory level is the hallmark

24
Q

What picture do hemi-cord lesions present

A

Brown sequard

25
Q

Describe the Brown sequard picture

A
Dorsal column loss (joint position sense and vibration) on the same side as the lesion 
Spinothalamic loss (pain and temperature) on the opposite side of the lesion
26
Q

When might a dissociated sensory loss occur?

A

In cervical cord lesions

27
Q

Describe a dissociated sensory loss

A

Loss of joint position and vibration sense without the loss of pain and temperature

28
Q

What do peripheral neuropathies cause?

A

Distal weakness

29
Q

How does the weakness in Guillian barre present?

A

Distal weakness which ascends over time