spinal cord sydromes Flashcards

(37 cards)

1
Q

what is polio ?

A

an RNA virus that destructs the anterior horn
LMN lesion - so causes flaccid paralysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the classic presentation associated with polio ?

A

unvaccinated child that has febrile illness , with neuro illness that present 4 to 5 days later
associated with weakness more in the legs than in the arms
flaccid muscle tone
usually one leg is much smaller than the other

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the vaccines used to fight polio ?

A

salk vaccine - killing intramuscularly
Sabin vaccine - live attenuated oral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is the feature in the polio vaccine that counts for their efficacy ?

A

neutralizing antibodies in the circulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is werdnig hoffman disease?

A

it is a s type of spinal muscular atrophy , the mosyt severe form of it
associated with diffuse muscle atrophy and the classic finding is tongue fasiculations
floppy baby syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is the prognosis of werdnig hoffman disease ?

A

death in a few months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is multiple sclerosis ?

A

t cell mediated autoimmune disease against oligodendrocytes , usually in white woman in 20-30 year range

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is the most common presentation associated with MS ?

A

optic neuritis and INO
relapsing remitting manner

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is amyotrophic lateral sclerosis ?

A

combines UMN and LMN disease where there is degeneration of the anterior horn cells and the lateral corticospinal tract
with no sensory symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what type of incontinence is associated with MS ?

A

urge incontinence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

is MS UMN or LMN ?

A

UMN so is associated with hyperreflexia and a positive babinski sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the common cause of death associated with ALS ?

A

aspiration pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the treatment for ALS ?

A

riluzole , decrease glutamate release

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the causes of familial cases of ALS ?

A

zinc copper superoxide dismutase defeciency
increased free radical release
SOD1 mutation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is the classic presentation of ALS ?

A

50 year old patient that has arm weakness
some flaccid muscle some spastic muscles
dysphagia
no sensory symptoms

17
Q

how is polio transmitted ?

A

feco oral transmission

18
Q

what is the pathology associated with ASA occlusion ?

A

anterior spinal artery occlusion is associated with loss of all except posterior columns , so only vibration and proprioception is intact

19
Q

what is the initial presentation of ASA occlusion ?

A

iniitially spinal shock
flaccid bilateral paralysis below the lesion
weeks later

spastic paralysis below the level of the lesion
bilateral loss of pain and temperature below the lesion

20
Q

what is the most common cause associated with ASA occlusion ?

A

aortic aneurysm repair

21
Q

what does the ASA supply ?

A

the anterior 2/3 of the spinal tract
corticospinal tract
spinothalamic tract
anterior horn cells

no dorsal column supply - thats the posterior spinal artery

22
Q

what is tabes dorsalis ?

A

degenration of the dorsal column due to syphillus , leading to bilateral loss of vibration and proprioception

23
Q

what are the positive findings associated with tabes dorsalis ?

A

ataxia ( wide based gate) with a positive romberg test
argyll robertson pupil
shooting pain
charcot joint

24
Q

what is syringiomyelia ?

A

fluid filled cavity within the spinal cord that usually happens between C2 and T( , results in a loss of pain and temperature in a cape like fashion ( from C5 to T4)

25
what malformation is associated with syringomyelia ?
chiairi malformation I kyphoscoliosis
26
what structure is compressed in syringomyelia ?
anterior white commissure
27
where can syringomyelia expand to ?
can expand to the anterior horn cells - LMN or lateral horn - give horner syndrome
28
what is subacute combined degeneration ?
neurological degeneration of the spinocerebellar tract corticospinal tract dorsal column (SCD) B12 deficiency
29
what is the classic presentation associated with SCD ?
problems walking in high risk groups can present as reversible dementia
30
what is brown sequard syndrome ?
loss of half of the spinal cord due to trauma or tumor
31
what is the presentation of brown sequard syndrome ?
at the site of lesion there is loss of all sensations along with LMN signs below the level of the lesion there are UMN signs and loss of vibration and proprioception on the contralateral side of the lesion there is loss of pain and temperature
32
when is horner syndrome associated with brown sequard syndrome ?
when the level of the lesion is above T! due to affection of the oculosympathetic pathway
33
where is the cauda equina ?
nerves below the conus medullaris
34
35
what is the cause of cauda equina and what are the associated findings ?
cause is usally due to herniation of the disc or metastasis to the spine presents with asymmetric saddle anesthesia urinary retention LL neuro findings severe lower back pain
36
what is conus medullari syndrome ?
injury to T12 to L2
37
what is the classic presentation associated with conus medullaris syndrome ?
perianal anesthesia sudden onset of bilateral leg weakness impotence