Neuro 8 Flashcards

(48 cards)

1
Q

What is transverse myelitis and what disease is it associated with

A

Multiple sclerosis

  • Area of inflammatory demyelination in the spinal cord
  • Motor and sensory loss below the level of the lesion with bowel and bladder dysfuntion
  • Initially flaccid paralysis followed by spastic paralysis with hyperreflexia
  • Patients may report a band of tingling or pain around the torso at the level of the lesion
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2
Q

What is Lhermitte’s sign

A

• Tingling, electric sensation down the spine when the patient flexes the neck

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3
Q

MRI findings in MS

A

♣ Periventricular plaques (areas of oligodendrocyte loss and reactive gliosis)
♣ T2 hyperintense areas in the white matter of the brain or spinal cord

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4
Q

CSF findings in MS

A

♣ Increased protein

♣ Oligoclonal IgG bands

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5
Q

Tx of acute MS flares

A

corticosteroids

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6
Q

Chronic tx of MS

A

interferon beta

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7
Q

Sx of multiple sclerosis

A

Triad of sx (SIN):
• Scanning speech
• Intention tremor, Incontinence, Internuclear ophthalmoplegia
• Nystagmus
♣ Lhermitte sign
• Tingling, electric sensation down the spine when the patient flexes the neck
♣ Transverse myelitis
• Area of inflammatory demyelination in the spinal cord
• Motor and sensory loss below the level of the lesion with bowel and bladder dysfuntion
• Initially flaccid paralysis followed by spastic paralysis with hyperreflexia
• Patients may report a band of tingling or pain around the torso at the level of the lesion
♣ Sensory symptoms (numbness and paresthesia)
♣ Motor symptoms (paraparesis and spasticity)
♣ Bowel/bladder dysfunction

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8
Q

What are the 2 components of presentation of neuromyeltiis optica (NMO)

A

♣ Transverse myelitis:
• Area of inflammatory demyelination in the spinal cord
• Motor and sensory loss below the level of the lesion with bowel and bladder dysfuntion
• Initially flaccid paralysis followed by spastic paralysis with hyperreflexia
• Patients may report a band of tingling or pain around the torso at the level of the lesion

♣ Opitc Neuritis:
• Mildly painful loss of visual acuity in one eye
• Pain most prominent with eye movement
• Vision may be blurry with loss of color discrimination

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9
Q

Diagnosis of NMO

A

♣ Antibodies to aquaporin-4 channel

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10
Q

Treatment of NMO

A

♣ Steroids

♣ Chemotherapeutic agents

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11
Q

Pathophys of progressive multifocal leukoencephalopathy

A

o Caused by JC virus

o Leads to demyelination by infecting oligodendrocytes

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12
Q

Presentation of PML

A

o Characterized by dementia, focal cortical dysfunction, cerebellar abnormalities

Non-enhancing multifocal brain lesions

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13
Q

Causes of posterior reversible encephalopathy syndrome (PRES)

A

o Usualy develops in the context of rapidly developing HTN and eclampsia or due to immunosuppressants used in organ transplant

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14
Q

Presentation of Posterior reversible encephalopathy syndrome (PRES)

A

♣ Headache
♣ Altered consciousness (acute confusional state)
♣ Visual disturbances (cortical visual loss – blindness with preserved pupillary reactivity)
♣ Seizures

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15
Q

Presentation of PSP

A
  • Supranuclear ocular palsy (failure of vertical gaze), dysarthria, dysphagia, extrapyramidal rigidity, gait ataxia, dementia, pseudobulbar palsy, bradykinesia, cognitive and behavioral abnormalities
  • Earliest signs are falls and gait abnormality
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16
Q

Diagnose: acute painless monocular vision loss with cherry red spot

A

Central retinal artery occlusion

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17
Q

Diagnose: light flashes, floaters, or curtain across visual field

A

Detached retina

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18
Q

Presentation of central retinal vein occlusion

A

Painless, sudden vision loss

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19
Q

Presentation of myasthenic crisis

A
♣	Precipitating factors
•	Infection or sugery
•	Pregnancy or childbirth
•	Tapering immunosuppressive drugs
•	Medications 
♣	Signs/symptoms
•	Increased generalized and oropharyngeal weakness
•	Respiratory insufficiency/dyspnea
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20
Q

Tx of syphilis

21
Q

What are features of TB meningitis (other than CSF) that differentiate it from bacterial meningitis

A

Usually affects the basal meninges (at base of brain) - so more likely to present with CN palsies

Slower onset

22
Q

Describe CSF findings of TB meningitis

A
Cells = lymphocytes
Protein = high
Glucose = very low
23
Q

CSF of viral meningitis

A
Cells = lymphocytes
Protein = high
Glucose = normal
24
Q

What are the 2 things to think of with ring-enhancing lesions in AIDs patients

A

Toxoplasmosis

CNS lymphoma

25
Neurocysticercosis is caused by what?
Eating EGGS of taenia solium
26
Tx of neurocysticercosis
Albendazole
27
What is spinal shock?
Flaccid weakness and absent DTRs immediately after spinal cord injury Spasticity and other UMN signs will develop over the next few days to weeks
28
Hemispatial neglect is caused by damage to what?
Non-dominant parietal cortex (usually R side)
29
What is 1st, 2nd, and 3rd line tx for pseudotumor cerebri
o 1. Acetazolamide o 2. Surgical intervention for patients refractory to medications ♣ Lumboperitoneal shunting ♣ Optic nerve sheath decompression o 3. Serial lumbar punturs as a bridge for patients awaiting surgery
30
Enzyme deficient in Lesch Nyhan syndrome
HGPRT (hypoxanthine-guanine phosphoribosyl transferase)
31
Clinical features of post-concussive syndrome
♣ HA, dizziness, sleep disturbance, cognitive impairment, behavioral abnormalities (e.g. irritability)
32
Tx of post-concussive syndrome
♣ Focus on individual components of syndrome with tx of each separately
33
Describe presentation of Guillain-Barre
♣ Ascending symmetrical paralysis over days to weeks ♣ Absent/depressed deep tendon reflexes ♣ Paresthesias ♣ Autonomic dysfuction (e.g tachycardia, urinary retention, and arrhythmias) occur in 70% of patients ♣ Respiratory compromise
34
CSF for Guillain Barre
♣ High protein with few cells
35
Tx of Guillain Barre
♣ IV immunoglobulin or plasmapheresis
36
What do you think when you see periodic sharp waves on EEG in a demented patient
CJD
37
What will you see in CSF of CJD patient
protein 14-3-3
38
Other than dementia, what are the other clinical features of CJD
• Rapidly progressive dementia + ataxia + startle myoclonus
39
What 2 diseases are associated with transverse myelitis
MS and NMO
40
What is Gerstmann syndrome and damage to what part of the brain is it caused by
Damage to dominant parietal lobe ♣ 1. Agraphia (inability to write) ♣ 2. Acalculia (inability to calculate) ♣ 3. Finger agnosia (inability to distinguish fingers) ♣ 4. Left-right disorientation
41
Damage to PPRF causes what?
Eyes look away from side of the lesion
42
Tx of tension HA
NSAIDs, Acetaminophen
43
Tx of cluster HA
100% O2, sumatriptan
44
Presentation of fetal hydantoin syndrome
o Caused by exposure to anticonvulsants (e.g. Phenytoin and Carbamazepine) o Midfacial hypoplasia, microcephaly, cleft lip and palate, digital hypoplasia, hirsutism, and developmental delay
45
What is the reticular activating system and where is it located
Located in the midbrain Mediates consciousness and alertness
46
Tx of status epilepticus
IV Benzos Phenytoin IV Phenobarbital
47
What is Fioricet
Caffeine, Acetaminophen, Butalbital Used for tension or muscle contraction HA
48
What part of CNS does pronator drift test for?
Pyramidal/corticospinal tract - UMN lesions cause more weakness in supinator muscles compared to pronator muscles