Clinical Syndromes of the Spinal Cord Flashcards

1
Q

Caused by:

  1. fracture/dislocation trauma by MVA, dive in pool, fall off horse, etc, usually in the cervical region, or bullet/knife wound
  2. demyelinating disease-MS, post-infectious transverse myelitis
  3. compression by tumor or inflammatory mass
A

Complete Transection

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2
Q

An acute syndrome of complete transection elicits

A

Spinal Shock

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3
Q

Can last several weeks, and consists of loss of all sensation, flaccid paralysis, loss of reflexes, and no bowel/bladder function

A

Spinal Shock

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4
Q

Chronically, with complete transection, there will emerge hyper-active reflexes (clonus) and increased tone, which together we term

A

Spasticity

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5
Q

Over time there will be flexor spasms, set off by simple

A

Cutaneous stimulation

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6
Q

If the lesion is sacral, the bladder will distend and overflow causing emptying with

A

Chronic infection

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7
Q

A spinal hemisection, example C4 level, is called

A

Brown Sequard Syndrome

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8
Q

Ipsilateral corticospinal tract-UMN syndrome with weakness of arm and leg, mild atrophy, hyper-reflexia (clonus of ankle), Babinski sign, and loss of abdominal and anal wink

A

Brown Sequard Syndrome

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9
Q

With Brown Sequard syndrome we see loss of Ipsilateral (dorsal) dorsal column

A

Position and Vibration

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10
Q

With Brown Sequard syndrome we see contralateral loss of

A

Pain (pin) and Temperature

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11
Q

With Brown Sequard syndrome we see the autonomic affects of

A

Horner’s Syndrome (miosis, ptosos, and anhydrosis)

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12
Q

With Brown Sequard syndrome at the C4 level, we see complete loss of

A

Motor and sensory root function

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13
Q

C4 level exhibits complete loss of motor and sensory root functions including sensation in dermatomal pattern if

A

2 roots

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14
Q

Partial Compression-Extra-axial, Extra-Medullary=

A

Pain

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15
Q

Pain and paresthesias, loss of pin, temperature, position, and vibration in C6/C7 dermatome; reduced triceps reflex

A

C6-C7 Dorsal root compression

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16
Q

Ipsilateral loss of position and vibration on arm and upper torso

A

C6-C7 dorsal column compression

17
Q

Ipsilateral UMN signs: increased tone and reflexes in triceps (not biceps), knee, and ankles with Babinski sign

A

C6-C7 Corticospinal Tract Compression

18
Q

Loss of ipsilateral lower motor neurons: segmental muscle weakness

A

C6-C7 Ventral Horn COmpression

19
Q

Cavitation near the central canal of the spinal cord

A

Syringomyelia/Central Cord Syndrome

20
Q

Caused by developmental, vascular (AVM), trauma, infections, astrocytic tumor, congenital malformations

A

Syringomyelia/Central Cord Syndrome

21
Q

Syringomyelia/Central Cord Syndrome most commonly occurs from

A

C3 to T4

22
Q

Initially experience a cape (shawl) distribution of lost spinothalamic fibers crossing at the ventral commissure, giving rise to reduced pin and temperature over lateral arms, forearms and fingers

A

Syringomyelia/Central Cord Syndrome

23
Q

Mechanical compression injury of the spinal cord with white matter injury, edema, and possible neuronal cell loss most commonly in the cervical region

A

Central Cord Syndrome

24
Q

Has the signs and symptoms of motor impairment, (arms greater than legs), and sensory loss below the level of the injury

A

Central Cord Syndrome

25
Q

The injury mechanism for central cord syndrome is usually

A

Age dependent

26
Q

High-energy events that cause fracture dislocations or disc herniation; includes motor vehicle accidents, falls, athletic and diving injury, gunshot wounds, assaults

A

Central Cord Syndrome in those younger than 45

27
Q

Low-energy hyperextension events that cause buckling of the ligamentum flavum; in the face of varying degrees of cervical spondylosis, cervical stenosis, spinal flexibility

A

Central Cord Syndrome in those older than 45

28
Q

MRI gradient T2 echo will reveal hyperintense signal in cervical cord and evidence of compression with

A

Central Cord Syndrome

29
Q

Atrophic weakness of hands/forearms; spasticity of legs; generalized hyperreflexia; a mixed UMN and LMN disorder progressive spread both rostrally and caudally until fatal

A

Atrophic Lateral Sclerosis (ALS)

30
Q

LMN signs with loss of strength, reduced tone, atrophy and loss of reflexes, all due to muscle denervation

A

ALS

31
Q

Some of these LMN signs of ALS are apparently reversed by appearance of hyper-reflexia from loss of

A

UMN Innervation

32
Q

Most common initial symptoms: stiffness/weakness and muscle wasting of hands/fingers, hand cramping, and later twitching of forearms (fasciculations)

A

ALS

33
Q

With ALS, only upper and lower motor neurons are affects and there is NO

A

Sensory involvement

34
Q

Due to vitamin B12 deficiency

A

Subacute combined degeneration

35
Q

Most affected by subacute combined degeneration

A

Dorsal columns (corticospinal tract is second)

36
Q

Because B12 deficiency also causes peripheral neuropathy, there may be the paradoxical combination of

A

Extensor plantar reflex (UMN sign) and hypoactive ankle (LMN sign)

37
Q

The great radicular artery of adamkiewicz is located at

A

T12-L2