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169 Cards in this Set

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meningeal layers
skull - (epidural space) - dura - (subdural space) - arachnoid - (subarachnoid space) - pia
Meningioma Origin
arachnoidal/meningiothelial cells on top of arachanoid granulations
Aging arachnoid
deposition of collagen
Virchow-Robin space
pia layer surrounding vessels which is continuous with the subarachnoid space
Nissl substance
endoplasmic reticulum in neurons
Cortical layers
1. molecular
2. external granular
3. external pyramidal
4. internal granular
5. internal pyramidal
6. plexiform
Brain areas most sensitive to hypoxic injury
CA1 region of the hippocampus
Purkinje cells in the cerebellum
Lipofuscin
oxidized fatty acids that accumulate in motor neurons.
normal aging process
Reactive astrocytes
activated astrocytes that respond to injury
Position of oligodendrocytes
in white matter: parallel sheets to axons
in grey matter: round neuronal cell bodies
Perivascular spaces
outside the virchow-robin space
common site for gliomas
Ependymal cells
line brain ventricles and central canal
cuboidal w/tight junctions
no basal lamina
Multiple Sclerosis
CNS demyelinating disease
episodic neurologic dysfunction
eventual persistent neuro deficits
MS epidemiology
onset btwn 15-45
Women 2:1
higher prevalence in temperate regions
MS symptoms
focal weakness (UMN signs)
paresthesias
dyscoordination, tremors
bladder spasticity
clinical progressions of MS
relapsing remitting
- eventually becomes 2dary progressive
Primary progressive (smooth progression)
MS characteristic lesions
acute: gadolinium-enhancing lesion
chronic: black hole
MS lesion types
Type1/Type2: perivenular myelin loss, preservation of oligodendrocytes
type 2-IgG/complement deposition
Type3/Type4: macrophage and T cell infiltration, no preservation of oligodrendrocytes
MS dopplegangers
Lyme disease
sarcoidosis
B12 deficiency
HIV
Dawson's fingers
perivenular demyelination perpendicularly oriented to ventricles in MS
MS spinal cord lesions
1-2 segments long
sensory symptomes
ambulation difficulty
loss of arm coordination
Evoked responses
Measured velocities of visual pathway action potentials
Slowed in MS
Oligoclonal IgG bands
IgG which is present in CSF but not in sera
present in 80-90% of MS cases
Steps of MS neuropathogenesis
CNS entry of activated Tcells, monocytes
Neuroinflammation
Axonal Degeneration
Gender incidence in Brain tumors
Gliomas and embryonal tumors occur more in males
Meningiomas occur more in females
Environmental Risk Factors for brain tumors
Radiation exposure
Consequences of brain herniation
blood vessel compression --> infarction and edema
Duret hemorrhages:stretching and tearing of brainstem vasculature
Nerve compression
Gliomas
tumors of neuroepithelial origin
Astrocytomas
Oligodendrogliomas
Ependymomas
Infiltrating Astrocytomas
Diffuse (grade II)
Anaplastic (grade III)
Glioblastoma (grade IV)
Diffuse Astrocytoma
Grade II tumor
diffusely invades the cerebrum
hypercellular, but nomitoses visible
Gemistocytic Astrocytoma
A diffuse astrocytoma containing plump cells with glassy pink cytoplasm
Anaplastic Astrocytoma
Grade III tumor
Increased cell density and pleomorphism
mitotic figures are now seen
can arise from diffuse tumor or be de novo
Glioblastoma
grade IV tumor
Areas of pseudopalisading necrosis
glomeruloid vascular changes
Glioblastoma genes
EGFR amplification: seen in primary GBM

TP53 mutation: seen in primary and secondary GBM
Pilocytic Astrocytoma
Mostly in kids, good prognosis
biphasic architecture: microcystic and solid compartments
Rosenthal fibers seen w/in astrocytes
Oligodendroglioma
Fried-egg cells with chicken-wire capillaries
Ependymoma
ependymal cell tumor
pseudorosettes around vessels
Embryonal Tumors
Malignant Grade IV tumors seen in kids. Includes medulloblastoma
Medulloblastoma
cerebellar tumor
"round blue" tumor (due to cell appearance)
rosettes may be present
Meningioma
Mostly benign and arise from meninges
may arise in NF1 and NF2
Schwannoma
in cranial nerves, most commonly affects CN VIII
bilateral vestibular schwannomas indicate NF2
Neurofibroma
may be dermal or intraneural
occurs in periphery
multiple tumors indicates NF1
wavy nuclei and comma-shaped cells
Cephalhematoma
bleed above the bone
doesn't cross suture lines
Linear Fracture
secondary to contact with large flat object
Facture begins along inner table
Compound Fracture
fracture associated with scalp laceration
Complex fracture
Fracture involving multiple bones
Depressed Fracture
secondary to contact with small objects
Contrecoup fracture
located distant from point of injury
Hinge Fracture
A francture extending across skull base
typically from car accidents
lethal
Contusion
a surface injury
Coup contusions
caused by bending at site of injury
moving object strikes stationary but movable head
Contre coup contusions
located distant from impact
Mechanisms:
1. impact -moving head strikes fixed object
2. impulsive loading-head set in motion/moving head is stopped
Types of DIffuse Brain Injury
Diffuse axonal injury
Concussion
Brain Swelling
Retraction Balls
ends of cut axons
Evidence of axonal injury from trauma
Severe Concussion effects
high glu, lactate, and intracellular calcium
Hyperextension of head
transects the caudal pons
Optic nerve sheath hemorrhages
often found in shaken baby syndrome
Total CSF Volume
Adult: 90-150 ml
neonate: 10-60 ml
Rate of CSF formation
500 ml per day
Difference between plasma and CSF
CSF has much lower protein, glucose, and potassium content
Arachnoid granulations
absorb CSF from subarachnoid space into venous circulation
Physiologic Roles of CSF
physical support
protection
extracellular homeostasis
excretory waste function
CSF formation
Ultrafiltration of plasma across capillary wall
then, choroid epithelial cells transport components into the ventricle
Blood-brain barrier
tight junctions between endothelial cells
thick basement membrane
astrocyte endfoots
Blood-brain permeability
permeable to water, uncharged lipid-soluble molecules
Circumventricular organs
exceptions to blood-brain barrier
sample the plasma and release hormones into blood
When to do a lumbar puncture
CNS infection
Subarachnoid hemorrhage
CNS malignancy
Demyelinating disease
Normal CSF opening pressure
Adult: 90-200 mm water
child: 10-100 mm water
if elevated, may be infection
Lumbar puncture contraindication
raised intracranial pressure
Lumbar punture side effects
headache for 2-14 days
Normal CSF cell counts
WBCs: 0-5 cell/ul
too many neutrophils, could be bacteria
too many lymphocytes, could be viral
RBS: 0 cell/ul
Pleocytosis: elevation of cell counts, often due to infection
Normal CSF glucose
60 mg/dl
if decreased, due to increased anaerobic glycolysis by parenchyma and leukocytes
CSF protein
Normal: 30 mg/dL
increased CSF protein: increased permeability, IgG synthesis
Meningitis presentation
fever, headache
altered mental status
stiff neck
photophobia
Viral meningitis families
Enteroviruses
Herpesviruses
Arboviruses
Transport of infection to CNS
hematogenous spread
local extension for paranasal sinuses
retrograde transport from PNS
direct implantation
pachymeningitis
infection of dura mater
leptomeningitis
inflammation of pia and arachnoid
encephalitis
inflammation of brain parenchyma diffusely
often viral
cerebritis
inflammation of brain parenchyma focally
often bacterial
myelitis
inflammation of spinal cord
poliomyelitis
inflammation of spinal grey matter
ganglionitis
inflammation of dorsal root ganglia
radiculitis
inflammation of intradural spinal nerve roots
Cryptococcal meningitis
most common fungal CNS infection
usually immunosuppresse
invade virchow-robin spaces
attach endothelium
Zygomycosis (Mucor)
often in diabetic ketoacidosis
basal brain and olfactory bulbs
medical emergency
Blastomycosis
spreads from lungs to brain
endemic in SE USA
Candidiasis
Opportunistic CNS infection
hemorrhagic infarcts
absesses
TB in CNS
forms granulomas in brain and spinal cord
Neuroborreliosis
lyme disease in the brain
causes aseptic meningitis
Brain Absesses
often Staph or strep
surrounded by fibrotic capsule
Toxoplasmosis
opportunistic infection
creates brain absesses
Entamoeba histolitica
an amoeba causing brain abscesses
Cysticercosis
injestion of tapeworm eggs can lead to chronic abscesses in brain
Empyema
subdural abscess.
Epidural Abscess
ex. Pott's disease (TB in spine)
Pathologic features of viral encephalitis
perivascular/parenchymal lymphocytic infiltrates
scattered glial nodules
neuronophagia
viral inclusion bodies
HSV-1 encephalitis
bilateral temporal lobe infection
Negri Bodies
red inclusions found w/rabies in neurons
Poliomyelitis
infection of anterior horns
Naegleria fowleri
amoeba that lives in soid, water
causes acute meningoencephalitis
netty pot disease
Cerebral malaria
causes circulation problem in brain
HIV encephalitis
HIV infects microglia
multinucleated giant cells
Progressive Multifocal Leukoencephalopathy
caused by JC virus
white matter disease
Contact loading results
contusion and hematoma
Inertial loading
head rotation
midline injury
diffuse asxonal injury
shrinking of tissue
TBI recovery
spatial memory often recovered
Seizure definition
transient dysfunction of all/part of brain due to excessive discharge of neurons, causing sudden and transient symptoms
Epilepsy definition
recurrent unprovoked seizures
Phenobarbital
Barbituate used to treat epilepsy
activates GABA-A receptors
Electroencephalography
surface readings of brain's extra-cellular current
mainly reflects summed excitatory/inhibitory synaptic input to pyramidal cells
Overall Seizure Types
Generalized
Focal
Types of Generalized seizures
Absence
Myoclonic
Tonic-clonic
tonic
clonic
atonic
Absence seizure
sudden arrest of activity, staring, and unresponsiveness
Myoclonic seizure
quick muscle jerks involving shoulders and arms
Tonic-clonic seizure
(grand mal)
generalized convulsion
bilateral extremity extension and muscle stiffening, then progression to bilateral extremity rhythmic shaking
Tonic seizure
bilateral extremity extension and muscle stiffening
Clonic seizure
bilateral extremity rhythmic shaking
Atonic seizure
sudden loss of neck/trunk tone, usually associated with falling
Seizure symmetry
generalized: symmetric
focal: begin asymmetrically
Focal seizure types
without impairment of awareness
with impairment of awareness
evolving to bilateral convulsive seizure
Frontal Lobe focal seizures
motor cortex: clonic shaking of contralateral limb
premotor: complex, bilateral motor activity
broca's: epresive language dysfunction
fronto-polar: absence
Temporal lob focal seizure
aura, arrest of activity, unresponsiveness, motor automatisms
Parietal lobe focal seizure
no typical form
occipital lobe focal seizure
visual signs, positive or negative
Childhood absence epilepsy
absence seizures presenting in childhood
treated with ethosuximide
hight risk of psychologic comorbidities
paroxysmal depolarization shift
abnormally prolonged calcium-dependent depolarization
causes a burst of depolarizations
possible origin of focal seizure
Repetitive EPSPs and IPSPs
EPSP: sum over time
IPSP: decline over time
Sustained Repetitive Firing
Inward sodium current causes bursts of action potentials
(similar to PDS, but with Na instead of Ca)
Generalized seizure mechanisms
Thalamocortical tracts
T-type Ca channels create generalized bursts (separate channel from PDS)
Mechanisms of Early Onset Epilepsies
GABA is excitatory in development, and NMDA receptors develop before AMPA receptors
Sodium channel blockers
phenytoin, carbamazepine, oxcarbazepine, lamotrigine
inhibits sustained repetitive firing -> epilepsy drug
GABA agonists
Barbiturates and Benzodiazepines
can be used as epilepsy treatment
Barbiturates
prolong GABA channel openings
Benzodiazepines
increase frequency of GABA-mediated chloride channel openings
T-type calcium channel blockers
ethosuximide, valproic acid
effective at treating specific epileptic subtypes
Excitatory Amino Acid Transmitter Antagonists
AMPA antagonist: topiramate
voltage-dependent Ca and Na: zonisamide
NMDA antagonist: felbamate
Axonal Stretch Injury
breaks microtubules
eventual degradation of microtubules
sodium channel opening, Na and Ca influx
repetitive TBI effects
massive Ca influx leads to increased Na channel density -> axon dysfunction and degeneration
30% of TBI injuries result in amyloid plaques extracellularly

Increased risk of Alzheimer's
n/a
Dementia pugilistica
Professional football player dementia
increased neurofibrillary tangles
Master Biological Clock
Suprachiasmatic Nucleus
Circadian clock adjustors
retinal receptors -> detect light levels -> low = melatonin
Polysomnography
EEG and other recordings during sleep
Cetacean Sleep
marine mammals sleep one brain-hemisphere at a time
VLPO
the sleep switch in the hypothalamus
sends GABA signals to arousatory centers
Sleep changes across the lifespan
as you age, more time awake and in stage 1 sleep
Sleep latency
the amount of time it takes to fall asleep
becomes shorter under sleep deprivation
Blink Speed
measures sleepiness
slower blink = more sleepy
Sleep debt
Neurobehavioral deficits accumulate linearly with sleep deficits
Actigraphy
patient wears a motion-detecting bracelet while asleep
Narcolepsy tetrad
hypersomnolence
cataplexy
hypnogogic/hypnopompic hallucinations
sleep paralysis
sleep latency
amount of time needed to fall asleep
normal = 10 minutes
Multiple Sleep Latency Test
4-5 20 minute naps at 2-hour intervals
typically no REM sleep
Cataplexy
sudden loss of muscle tone triggered by emotions
Narcolepsy Pathophysiology
Boundaries between wakefulness and REM sleep are not well-maintained
Due to reduced hypocretinergic neurons
Modafinil/armodafinil
Narcolepsy drugs
Cataplexy drugs
Tricylic antidepressents
SSRIs
gamma hydroxybutyrate
Parasomnia
an undesirable behavioral, motor, or sensory phenomenon which occurs intermittently during sleep
Disorders of Arousal
Confusional Arousals
Sleepwalking
Sleep Terrors
All occure in non-REM sleep
Treatment for disorders of arousal
Mostly non-pharmacological
benzodiazepines
REM Sleep Behavior DIsorder (RBD)
violent dream-enacting w/tonic activity in REM sleep
Likely a pontine dysfunction
RBD causes
Narcolepsy
Neurodegenerative disease (parkinsonisms)
Anti-depressants
RBD treatment
Clonazepam suppresses behaviors
Restless Legs vs. Periodic Limb Movements
Restless legs: awake sensory phenomenon w/volitional motor response
PLM: involuntary sleep-related motor phenomenon
RLS exacerbations
psychological stress
physical confinement
caffeine
poor sleep
Secondary RLS associated conditions
Iron deficiency anemia
Pregnancy
Chronic Renal Failure
RLS pathophysiology
low Fe availability in brain -> impaired dopamine tranmission -> lowered supra-spinal inhibition
(speculation)
RLS treatments
Dopamine Agonists
Opiates
gabapentin
iron
benzodiazepines