DIT review - Neurology 3 Flashcards

1
Q

What is the cause and presentation of central pontine myelinolysis

A
  • Due to rapid correction of hyponatremia leading to massive axonal demyelination in pontine white matter
  • MRI will show increased signal intensity in the pons
  • Presentation:
    • Acute paralysis, dysarthria (difficulty speaking), dysphagia (difficulty swallowing), diplopia (double vision), loss of consciousness
    • Can cause “locked in syndrome” – preserved consciousness with paralysis except for eye movement
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2
Q

What will be seen in a CN V motor lesion

A
  • Jaw deviates towards side of lesion
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3
Q

What will be seen in CN X lesion

A
  • Uvula deviates away from side of lesion
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4
Q

What will be seen in CN XI lesion

A
  • Weakness turning head contralateral to lesion (SCM)
  • Shoulder droop on side of lesion (trapezius)
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5
Q

What will be seen in CN XII lesion?

A
  • Tongue deviates toward side of lesion (“lick your wounds”)
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6
Q

Describe the difference between an UMN and LMN lesion of the facial nerve

A
  • Upper motor neuron lesion - more severe, could mean stroke
    • Destruction of motor cortex or connection between motor cortex and facial nucleus
    • Contralateral paralysis of lower facial muscles (sparing of forehead)
  • Lower motor neuron lesion - Bell’s Palsy
    • Destruction of facial nucleus or facial nerve
    • Ipsilateral paralysis of upper and lower muscles of face
  • Explanation:
    • Facial motor nucleus receives motor fibers for the lower face from the opposite motor cortex and motor fivers for the upper face from both moto cortices
    • So if a lesion occurs in the L motor cortex facial region, there is still sufficient innervation for R upper face from R motor cortex
    • But since L motor cortex is the only innervation of R lower face, there will be paralysis of R lower face
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7
Q

What are the 4 midline structures and associated lesion presentations in the midbrain

A

Motor pathway - contralateral weakness

Medial lemniscus - contralateral proprioception/vibration deficit

Medial longitidinal fasciculus - ipsilateral internuclear ophthalmoplegia

Motor nuclues and nerve - ipsilateral CN motor loss (3, 4, 6, 12)

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8
Q

What are the 4 lateral structures and associated lesion presentations of the brainstem?

A

Spinocerebellar - ipsilateral ataxia

Spinothalamic - contralateral pain and temp

Sensory V - ipsilateral pain and temp of the face

Sympathetic - ipsilateral Horner’s

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9
Q

Describe the blood supply of the brainstem (medial and lateral of midbrain, pons, and medulla)

A
  • Midbrain:
    • Medial - posterior cerebral
    • Lateral - posterior cerebral
  • Pons:
    • Medial - Basilar
    • Lateral - Anterior inferior cerebellar artery (AICA)
  • Medullar:
    • Medial - anterior spinal (ASA)
    • Lateral - Posterior inferior cerebellar artery (PICA)
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10
Q

What will you see if you have a lesion of the left medial longitudinal fasciculus (MLF)?

A

You will have no problem when looking L, but when looking R, the L eye will not move medially (problem of the L medial rectus muscle)

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11
Q

What is the other term for lesion of the MLF?

A

Internuclear ophthalmoplegia

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12
Q

What is the cause and presentation of Weber syndrome?

A
  • Lesion of medial midbrain
    • Caused by posterior cerebral artery
    • Presentation:
      • Contralateral spastic paralysis or hemiparesis
      • CN III palsy (eye turned down and out)
      • Ptosis (CN III)
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13
Q

What is the cause and presentation of Wallenberg syndrome

A
  • Lesion of lateral medulla
    • Caused by posterior inferior cerebellar artery (PICA)
    • Presentation:
      • Dysphagia, hoarseness, decreased gag reflex (CN IX and X)
      • Ipsilateral loss of pain and temp of the face
      • Contralateral loss of pain and temp of the body
      • Ipsilateral Horner syndrome
      • Ipsilateral cerebellar defects
      • Vertigo, nystagmus, nausea, vomiting (CN VIII since defect is upper medulla)
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14
Q

Lesion of what artery can cause locked-in syndrome

A

This is a lesion of the medial pons – basilar artery

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15
Q

What will you see on spinal tap in a subarachnoid hemorrhage

A

Bloody or yellow (xanthochromic) tap

Yellow = breakdown of hemoglobin from blood into bilirubin

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16
Q

What are the layers that you go through during a spinal tap?

A

Skin - superficial fascia - supraspinous ligament - interspinous ligament - ligamentum flavum - epidural space - dura mater - subdural space - arachnoid membrane - subarachnoid space (this is where CSF is)

17
Q

Most common location of berry aneurysm

A

Junction of anterior communications and anterior cerebral artery

18
Q

Diseases associated with berry aneurysm

A

Ehlers-Danlos syndrome

Autosomal dominant polycystic kidney disease

19
Q

Describe the flow of CSF

A
  • Ependymal cells of choroid plexus make CSF - lateral ventricles - foramine of Monro - 3rd ventricle - cerebral aqueduct - 4th ventricle - foramine of Luscka + foramine of Magendie - subarachiod space - reabsorption via arachnoid granules - dural venous sinuses
20
Q

What is the basic premise behind pseudotumor cerebri?

A
  • Aka idiopathic intracranial HTN
  • Increased intracranial pressure without hydrocephalus
21
Q

Risk factors and presentation of pseudotumor cerebri?

A
  • Risk factors:
    • Woman of childbearing age
    • Vitamin A excess
    • Tetracyclines
  • Presentation:
    • Headache, diplopia, papilledema
    • Lumbar puncture shows increased opening pressure with headache relief
22
Q

Treatment of pseudotumor cerebri

A
  • Weight loss
  • Acetazolamide
  • Repeat LP
23
Q

Describe the different types of hydrocephalus

A
  • Non-communicating
    • Due to obstruction/blockage of CSF flow (e.g. tumor or cerebral aqueduct stenosis)
  • Communicating:
    • Communicating hydrocephalus
      • Due to decreased absorption by arachnoid granulations (e.g. scarring post-meningitis)
    • Normal pressure hydrocephalus
      • Ventricular dilation with normal ICP
24
Q

What is disease associated with “wet, wacky, wobbly”

A

Normal pressure hydrocephalus

  • Urinary incontinence - wet
  • Dementia - wacky
  • Ataxia - wobbly
    • Magnetic gait – feet appear stuck on floor
25
Q

What is ex vacuo ventriculomegaly

A
  • Mimics hydrocephaly
  • Atrophy of brain tissue surrounding the ventricles makes ventricles appear dilated on imaging
    • ICP is normal
  • E.g. Alzheimer’s and Pick disease
26
Q

Describe cluster HA (duration, location, features, associated sx, treatment)

A
  • 15 min – 3 hours
  • Repetitive (often occur daily at the same time)
  • Unilateral, non-throbbing heading
  • Excruciating pain, usually perioribital
  • Associated with lacrimation, rhinorrhea, and Horner syndrome (ptosis and miosis, not anhidrosis)
  • Treatment: 100% O2, sumatriptan
27
Q

Describe tension HA (duration, location, features, associated sx, treatment)

A
  • Usually 4 – 6 hours
  • Bilateral headache with constant, steady pain
  • Usually in frontal or occipital lobe
  • No throbbing, no photophobia, no phonophobia, no aura
  • Treatment: NSAIDs, Acetaminophen
28
Q

Describe migraine HA (duration, location, features, associated sx, treatment)

A
  • Usually 4 – 72 hours
  • Unilateral pulsing, throbbing headache
  • Associated with nausea, photophobia, phonophobia, and aura
  • Treatment: Triptans
29
Q

What are the disorders associated with psammoma bodies?

A

THINK: PSaMMoma

Papillary thyroid carcinoma

Serous cystadenocarcinoma of the ovary

Meningioma

Mesothelioma

30
Q

Name all the adult and children brain tumors

A

Adult:

Glioblastoma multiforme

Meningioma

Oligodendroglioma

Schwannoma

Hemangioblastoma

Pituitary adenoma

Children:

Pilocytic astrocytoma

Ependymoma

Medulloblastoma

Craniopharyngioma

31
Q

Describe defining features of glioblastoma multiforme

A
  • Malignant tumor of astrocytes à GFAP (+)
  • Found in cerebral hemispheres and may cross corpus callosum – “butterfly lesion”
  • Pseudopalisading – tumor surrounding central necrosis
  • Poor prognosis
32
Q

Describe defining features of meningioma

A
  • Benign tumor of arachnoid cells
  • May present with seizures
  • Histology shows whorled pattern and psammoma bodies
33
Q

Describe defining features of hemangioblastoma

A
  • Associated with Von-Hippel Lindau syndrome (increased risk of bilateral renal cell carcinoma)
  • Can produce erythropoietin à secondary polycythemia
34
Q

Describe defining features of schwannoma

A
  • Benign tumor of Schwann cells à S-100 (+)
  • Most frequently involved CN VIII (loss of hearing and tinnitus)
  • Bilateral vestibular schwannomas seen in neurofibromatosis-2
35
Q

Describe defining features of oligodendroglioma

A
  • Most often in frontal love
  • “Fried egg” appearance (round nuclei with clear cytoplasm)
36
Q

Describe defining features of pilocytic astrocytoma

A
  • Benign tumor of astrocytes à GFAP (+)
  • Usually arises in posterior fossa
  • Cystic lesion with mural nodule
  • Rosenthal fibers – eosinophilic corkscrew fibers
37
Q

Describe defining features of medulloblastoma

A
  • Malignant tumor derived from neuroectodem
  • Can compress 4th ventricle leading to hydrocephalus
  • Homer Wright rosettes (small blue cells wrap around pink areas of neuritic processes)
38
Q

Describe defining features of ependymoma

A
  • Malignant tumor of ependymal cells (most often in 4th ventricle)
  • Can compress 4th ventricle leading to hydrocephalus
  • Perivascular pseudorosettes (tumor cells surrounding vessel)
39
Q

Describe defining features of craniopharyngioma

A
  • Derived from remnant of Rathke’s pouch (where anterior pituitary sprouted from mouth)
  • Supretentorial mass that may lead to bitemporal hemianopia
  • Often see calcifications (derived from “tooth-like” structures)