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338 Cards in this Set

  • Front
  • Back
What is derived from neuroectoderm?
(4)
- CNS neurons
- ependymal cells (inner lining of ventricles --> make CSF)
- oligodendroglia
- astrocytes
What is derived from neural crest?
(2)
- Schwann cells
- PNS neurons
What is derived from mesoderm?
(2)
- microglia
- macrophages

"Microglia, like Macrophages, originate from Mesoderm"
General info on Neurons?
- comprise nervous system
- permanent cells --> do not divide in adulthood

- large cells with prominant nucleoli
- Nissl substance (RER) in cell body, dendrites, NOT axon
General info on Astrocytes?
- physical support
- repair
K+ metabolism
- removal of excess NT
- maintenance of blood-brain barrier

- reactive gliosis in response to injury
What is the astrocyte marker?
GFAP
General info on Microglia?
- CNS phagocytes

- mesodermal origin
- not readily discernible in Nissl stains
- have small, irregular nuclei and relatively little cytoplasm

- microglia --(tissue damage--> large ameboid phagocytic cells
What happens to HIV-infected microglia cells?
- they fuse to from multinucleated giant cell in the CNS
General info on Oligodendroglia?
- each one myelinates multiple CNS axons (up to 30 each)
- in Nissl stains, they appear as small nuclei with dark chromatin and little cytoplasm
- predominant type of glial cell in white matter
-resemble fried egg on H&E
What cells are destroyed in Multiple Sclerosis?
Oligodendrocytes
General info on Schwann cells?
- each one myelinates only 1 PNS axon
- also promote axonal regeneration

- derived from neural crest
What cells are destroyed in Guillain-Barre syndrome?
Schwann cells
Acoustic Neuroma?
- type of schwannoma
- typically located in internal acoustic meatuc (CN VIII)
Free nerve endings types, location, function
1. C -- slow, unmyelinated fibers
2. Aδ -- fast, myelinated fibers

skin, epidermis, some viscera

sense pain and temperature
Meissner's corpuscles general info, location, function
- large, myelinated fibers

glabrous (hairless) skin

sense position, dynamic touch, adapt quickly
Pacinian corpuscles general info, location, function
- large, myelinated fibers

deep skin, ligaments, joints

sense vibration and pressure
Merkel's disks general info, location, function
- large, myelinated fibers

hair follicles

position sense, static touch (sharp edges), adapt slowly
Endoneurium
- invest single nerve fiber

- inflammatory infiltrate in Guillain-Barre
Perineurium
- Permeability barrier

- surrounds a fascicle of nerve fibers

- must be rejoined in microsurgery for limb reattachment
Epineurium
- dense connective tissue that surrounds entire nerve (fascicles and blood vessels)
NE and anxiety?
- NE is INCREASED in anxiety
NE and depression?
- NE is DECREASED in depression
Dopamine and schizophrenia?
- dopamine is INCREASED in schizophrenia
Dopamine and Parkinson's?
- dopamine is DECREASED in Parkinson's (and depression)
Dopamine and depression?
- dopamine is DECREASED in depression (and Parkinson's)
5-HT and anxiety?
- 5-HT is DECREASED in anxiety (and depression)
5-HT and depression?
- 5-HT is DECREASED in depression (and anxiety)
ACh and Alzheimer's?
- ACh is DECREASED in Alzheimer's (and Huntington's and REM sleep)
ACh and Huntington's?
- ACh is DECREASED in Huntington's (and Alzheimer's and REM sleeep)
ACh and REM sleep?
- ACh is DECREASED in REM sleep (and Alzheimer's and Huntington's)
GABA and anxiety?
- GABA is DECREASED in anxiety (and Huntington's)
GABA and Huntington's?
- GABA is DECREASED in Huntington's (and anxiety)
Where is NE synthesized?
Locus ceruleus
Where is dopamine synthesized?
Ventral tegmentum and SNc
Where is 5-HT synthesized?
Raphe nucleus
Where is ACh synthesized?
Basal nucleus of Meynert
Where is GABA synthesized?
Nucleus accumbens
What area of the brain makes NT in response to stress and panic?
- Locus ceruleus --> NE
What is the reward center, pleasure, addiction, fear center of the brain?
Nucleus accumbens and Septal nucleus
What NT are INCREASED in anxiety?
(1)
- NE
What NT are DECREASED in anxiety?
(2)
- 5-HT
- GABA
What NT are DECREASED in depression?
(3)
- NE
- dopamine
- 5-HT
What NT are DECREASED in Parkinson's?
(1)
- dopamine
What NT are DECREASED in Alzheimer's?
(1)
- Ach
What NT are DECREASED in Huntington's?
(2)
- ACh
- GABA
What NT are DECREASED in REM sleep?
(1)
- ACh
What 3 structures form the blood-brain barrier (BBB)?
1. Tight junctions between nonfenestrated capillary endothelial cells
2. Basement membrane
3. Astrocyte processes
What crosses the BBB slowly by carrier-mediated transport mechanism?
(2)
- glucose
- amino acids
What crosses the BBB rapidly via diffusion?)
- nonpolar/lipid-soluble substances
A few specialized brain regions with fenestrated capillaries and no BBB allow what?
(2)
1. they allow molecules in the blood to affect brain function (ie. area postrema --> vomiting after chemo; OVLT --> osmotic sensing)

2. they allow neurosecretory products to enter circulation (ie. neurohypophysis --> ADH release)
What are the 3 blood barriers?
1. blood-brain barrier
2. blood-testis barrier
3. maternal-fetal blood barrier of placenta
What does a brain infarction destroy in relation to the blood brain barrier? And what does this lead to?
- endothelial cell tight junctions

- leads to vasogenic edema
What does the Hypothalamus do?
"TAN HATS"

- Thirst and water balance
- Adenohypophysis control
- Neurohypophysis releases hormones from hypothalamus

- Hunger
- Autonomic regulation
- Temperature regulation
- Sexual urges
Inputs to the hypothalamus?
(2)
- OVLT (senses change in osmolarity)

- area postrema (responds to emetics)
What makes ADH?
Supraoptic nucleus
Where is the supraoptic nucleus found?
Hypothalamus
What makes oxytocin?
Paraventricular nucleus
Where is the paraventricular nucleus found?
Hypothalamus
What does the lateral area of the hypothalamus do?
controls hunger

destruction leads to anorexia, failure to thrive (infants)
What inhibits the lateral area of the hypothalamus?
Leptin --> don't feel hungry
What does the ventromedial area of the hypothalamus do?
controls satiety

destruction leads to hyperphagia

"If you zap your VENTROMEDIAL nucleus, your grow VENTRALLY and MEDIALLY"
What stimulates the ventromedial area of the hypothalamus ?
Leptin --> feel full
What does the Anterior hypothalamus control? And is it controlled via sympathetics or parasympathetics?
- cooling

- pArasympathetic

"Anterior nucleus = Cool off"
(A/C = Anterior Cooling)
What does the posterior hypothalamus control? And is it controlled via sympathetics or parasympathetics?
- heating

- sympathetic

"posterior nucleus = get fired up"

"If you zap your Posterior hypothalamus, you become a Poikilotherm (cold-blooded, like a snake)"
What does the Septal nucleus control?
Sexual urgers
Where is the septal nucleus located?
Hypothalamus
What does the suprachiasmatic nucleus control?
Circadian rhythm

"You need SLEEP to be CHARISMATIC (chiasmatic)"
Where is the suprachiasmatic nucleus located?
Hypothalamus
What are all the areas of the hypothalamus and what do they do?
(8)
1. Supraoptic nucleus -- makes ADH
2. Paraventricular nucleus -- makes oxytocin
3. Lateral area -- hunger
4. Ventomedial area -- satiety
5. Anterior hypo -- cooling
6. Posterior hypo -- heating
7. Septal nucleus -- Sexual urges
8. Suprachiasmatic nucleus -- circadian rhythm
Posterior pituitary aka?
Neurohypophysis
What does the posterior pituitary do?
- receives hypothalamic axonal projections from supraoptic (ADH) and paraventricular (oxytocin) nuclei
Anterior pituitary aka?
Adenohypophysis
Oxytocin
- made by paraventricular nuclei of hypothalamus

- oxys = quick
- tocos = birth
What does the Thalamus do?
- major relay for ascending sensory information that ultimately reaches the cortex
What does the Lateral geniculate nucleus (LGN) control?
- visual, CN II

- projects via optic radiations to occipital cortex

"Lateral for Lookin' "
Where is the lateral geniculate nucleus (LGN) located?
Thalamus
What does the Medial geniculate nucleus (MGN) control?
- auditory

receives input from superior olive and inferior colliculus of tectum

goes to auditory cortex of temporal lobe

"Medial for Music"
Where is the medial geniculate nucleus (MGN) located?
Thalamus
What does the ventral posterior nucleus, lateral part (VPL) do?
- body sensation (proprioception, pressure, pain, tough, vibration via dorsal columns, spinothalamic tract)
Where is the ventral posterior nucleus, lateral part (VPL) located?
Thalamus
What does the ventral posterior nucleus, medial part (VPM) do?
- facial sensation (via CNV) -> goes to primary somatosensory cortex

"You put Makeup on your face, and the sensory info is relayed through the VPM"
Where is the ventral posterior nucleus, medial part (VPM) located?
Thalamus
What does the ventral anterior/lateral (VA/VL) nuclei do?
motor

"Motor is anterior to sensation in the thalamus, just like the cortex"
Where is the ventral anterior/lateral (VA/VL) nuclei located?
Thalamus
Blood supply to the thalamus?
- posterior communicating artery
- posterior cerebral artery
- ICA (anterior choroidal arteries)
What all does the LImbic system include?
(4)
- cingulate gyrus
- hippocampus
- fornix
- mammillary bodies
What all is the Limbic system responsible for?
(5)
"The Famous 5 F's"

- Feeding, Fighting, Fleeing, Feeling, and *******
What info does the cerebellum receive?
- receives CONTRAlateral cortical input via middle cerebellar peduncle

- receives IPSIlateral proprioceptive info via inferior cerebellar peduncle
What are the input nerves to the cerebellum?
- climbing and mossy fibers
What does the cerebellum do?
- provides stimulatory feedback to CONTRAlateral cortex to modulate movement
What are the output nerves from the cerebellum?
- Purkinje fibers output to deep nuclei of cerebellum --> which in turn output to cortex via superior cerebellar peduncle
What are the deep nuclei of the cerebellum?
Lateral to Medial:
- Dentate
- Emboliform
- Globose
- Fastigial

"Don't Eat Greasy Foods"
What does the lateral cerebellum control?
- voluntary movement of extremities
What does the medial cerebellum control?
- balance
- truncal coordination
- ataxia
- propensity to fall toward injured (IPSIlateral) side
In what areas is the basal ganglia important?
(2)
- voluntary movements
- making postural adjustments
SNc
- Substantia nigra pars compacta

- part of the basal ganglia
SNr
- Substantia nigra pars reticulata

- part of the basal ganglia
GPe
- Globus pallidus externus

- part of the basal ganglia
GPi
- Glubus pallidus internus

- part of the basal ganglia
STN
- Subthalamic nucleus

- part of the basal ganglia
D1
- Dopamine D1 receptor
- excitatory

"D1-R = D1Rect pathway"

- part of the basal ganglia
D2
- Dopamine D2 receptor
- inhibitory

"Indirect = Inhibitory"

- part of the basal ganglia
Excitatory pathway of the basal ganglia?
Cortex (stimulates via glutamate) → Striatum (inhibits) → "SNr-GPi" complex (less inhibition of thalamus) → Thalamus (stimulates) → Cortex (stimulates) → Muscles, etc. → (hyperkinetic state)

- SNc's dopamine binds to D1 receptors in the excitatory pathway --> stimulating the excitatory pathway (increases motion)

- therefore, loss of dopamine in Parkinson's inhibits the excitatory pathway (decreased motion)
Inhibitory pathway of the basal ganglia?
Cortex (stimulates) → Striatum (inhibits) → GPe (less inhibition of STN) → STN (stimulates) → "SNr-GPi" complex (inhibits) → Thalamus (is stimulating less) → Cortex (is stimulating less) → Muscles, etc. → (hypokinetic state)

- SNc's dopamine binds to D2 receptors in the inhibitory pathway --> inhibiting the inhibitory pathway (double negative) (increased motion)

- therefore, loss of dopamine in Parkinson's excites (ie. disinhibits) the inhibitory pathway ( decreased motion)
What is Parkinson's disease?
- a degenerative disorder or CNS
What is Parkinson's disease associated with (microscopically)?
(2)
- Lewy bodies (composed of α-synuclein --> intacellular inclusion)

- depigmentation of the substantia nigra pars compacta (SNc) --> loss of dopaminergic neurons
Rare cases of Parkinson's disease have been linked to what?
- exposure to MPTP --> a contaminant in illicit street drugs
What symptoms do you see in Parkinson's disease?
(4)
"TRAP"

- Tremor (at rest -- ie. pill-rollong tremor)
- cogwheel Rigidity
- Akinesia
- Postural instability

"you are TRAPped in your body"
What is hemiballismus?
- sudden, wild flailing of 1 arm +/- leg

"Half ballistic (as in throwing a baseball)"
What is hemiballismus characteristic of?
- contralateral subthalamic nucleus lesion (ie. *lacunar stroke in pt. with a history of HTN*)

- loss of inhibition of thalamus through globus pallidus
What is Huntington's disease?
- an autosomal dominant trinucleotide repeat disorder
- expansion of CAG repeats (anticipation)

"CAG = Caudate loses Ach and Gaba"
On what chromosome is the trinucleotide repeat found in Huntington's disease?
Chromosome 4
What happens in Huntington's disease?
Neuronal death via:

- NMDA-R binding
- glutamate toxicity
What symptoms do you see in Huntington's disease?
(3)
- Chorea (quick movements of feet of hands)
- Depression
- Progressive Dementia
When do symptoms manifest in Huntington's disease?
- between the ages of 20 and 50
What do you see on MRI in Huntington's disease?
- atrophy of caudate nucleus (loss of GABA)
- atrophy of putamen

- enlarged lateral ventricles
- defined sulci
What is chorea?
- sudden, jerky, pruposeless movements (of hands and feet)

- Chorea = dancing (Greek)
"Think choral dancing or choreography"
Chorea is characteristic of what?
- basal ganglia lesion (ie. Huntington's)
What is athetosis?
- slow, writhing movements, especially of fingers

- Athetos = not fixed (Greek)
"Think snakelike"
Athetosis is characteristic of what?
- basal ganglia lesion (ie. Huntington's)
What is myoclonus?
- sudden, brief muscle contraction

- jerks, hiccups
What is dystonia?
- sustained, involuntary muscle contractions

- writer's cramp
What is an Essential/Postural tremor?
- action tremor (worsens when holding posture)

- autosomal dominant

- essential trmor pts. often self-medicate with alcohol, which decreases tremor
What is the treatment for essential/postural tremor?
- β-blockers
What is a Resting tremor?
- most noticeable distally
- seen in Parkinson's pts (pill-rolling tremor)
What is an Intention tremor?
- slow, zig-zag motion when pointing toward a target
- associated with cerebellar dysfunction
Cerebral Cortex functions:
Frontal Lobe (4)
- Motor speech (Broca's area; dominant hemishpere)
- Frontal eye fields
- Premotor area (part of extrapyramidal circuit)
- Principle motor area
Cerebral Cortex functions:
Parietal Lobe (1)
- Principal sensory areas
Cerebral Cortex functions:
Occipital Lobe (1)
- Prnicipal visual cortex
Cerebral Cortex functions:
Temporal Lobe (2)
- Primary auditory cortex (Heschl's gyrus)
- Associative auditory cortex (Wernicke's area; dominant hemisphere)
What does the arcuate fasciculus connect?
- Wernicke's area (associative auditory complex) and Broca's area (motor speech)
Frontal Lobe functions
(9)
"Executive Functions"

1. planning
2. inhibition
3. concentration
4. orientation
5. language
6. abstraction
7. judgement
8. motor regulation
9. mood
What is most noticible symptom in frontal lobe lesions?
- lack of social judgement

"Damage = Disinhibition (ie. Phineas Gage)"
What is the homunculus?
- a topographical representation of sensory and motor areas in the cerebral cortex
What is the homunculus used for?
- used to localize lesions (ie. in blood supply) leading to specific defects

- for example, lower extremity deficit in sensation or movement may indicate involvement of the anterior cerebral artery
Brain Lesion Consequences:

Amygdala (bilateral)
(3)
Kluver-Bucy syndrome:

- hyperorality
- hypersexuality
- disinhibited behavior

associated with HSV-1
Brain Lesion Consequences:

Frontal Lobe
(5)
- contralateral spastic paresis
-disinhibition
- deficits in concentration, orientation, and judgement
- may have reemergence of primitive reflexes
-can result in Broca's aphasia if dominant hemisphere
Brain Lesion Consequences:

Right parietal lobe
(1)
- Spatial neglect syndrome (agnosia of the contralateral side of the world)
Brain Lesion Consequences:

Reticular activating system (midbrain)
(1)
- reduced levels of arousal and wakefulness (ie. coma)
Brain Lesion Consequences:

Mammillary bodies (bilateral)
(6)
Wernicke-Korsakoff syndrome

- Wernicke --> confusion, ophthalmoplegia, ataxia, can be secondary to thiamine deficiency

- Korsakoff --> memory loss, confabulation, personality changes
Brain Lesion Consequences:

Basal ganglia
(3)
- tremor at rest
- chorea
- athetosis
Brain Lesion Consequences:

Cerebellar hemisphere
(2)
- intention tremor
- limb ataxia

- damage to the cerebemmum results in IPSI deficits
- fall toward side of lesion
- cerebellum --> SCP --> contralateral cortex --> corticospinal decussation = IPSI

"Cerebellar hemispheres are LATERALLY located --> affect LATERAL limbs"
Brain Lesion Consequences:

Cerebellar vermis
(2)
- truncal ataxia
- dysarthria

"Vermis is CENTRALLY located --> affects CENTRAL body"
Brain Lesion Consequences:

Subthalamic nucleus
(1)
- CONTRA hemiballismus
Brain Lesion Consequences:

Hippocampus
(1)
- anterograde amnesia (inability to make new memories)
Brain Lesion Consequences:

Paramedian pontine reticular formation (PPRF)
(1)
- eyes look AWAY from side of lesion
Brain Lesion Consequences:

Frontal eye fields
(1)
- eyes look TOWARD lesion
What symptoms do you see in Central Pontine Myelinolysis?
(5)
- acute paralysis
- dysarthria
- dysphagia
- diplopia
- loss of consciousness
What commonly causes Central Pontine Myelinolysis?
- very rapid correction of hyponatremia
What happens with a recurrent laryngeal nerve injury?
- loss of all laryngeal muscle except cricothyroid
What symptom do you see in recurrent laryngeal nerve injury?
- hoarseness
What is aphasia?
- higher-order inability to speak
What is dysarthria?
- motor inability to speak
What is Broca's aphasia?
- NONFLUENT aphasia with intact comprehension

"BROca's BROken BOCA"

left MCA superior division most often produces lesion
Where is Broca's area?
- inferior frontal gyrus of frontal lobbe
What is Wernicke's aphasia?
- FLUENT aphasia with impaired comprehension

"Wernicke's is Wordy but makes no sense!"

"Wernicke's = What?"

left MCA inferior division most often produces lesion
Where is Wernicke's area?
- superior temporal gyrus of temporal lobe
What is global aphasia?
- NONFLUENT aphasi with impaird comprehension

- BOTH Broca's and Wernicke's areas affected
What is conduction aphasia?
- poor repetition but FLUENT speech
- intact comprehension
- Arcuate fasciculus -- connects Broca's and Wernicke's areas
What does the anterior cerebral artery supply?
- supplies anteromedial surface
What does the middle cerebral artery supply?
- supplies lateral surface
What does the posterior cerebral artery supply?
- supplies posterior and inferior surfaces
Associated area/deficit for:

Anterior spinal artery
(3)
Medial medullary syndrome

- CONTRA hemiparesis (lower extremities)
- medial lemniscus (decreased CONTRA proprioception)
- IPSI paralysis of hypoglossal nerve
Associated area/deficit for:

PICA
(12)
Lateral medullay syndrome (aka Wallenberg's)

Nucleus ambiguous (CN IX, X, XI): IPSI paralysis of larynx, pharynx, palate -> dysarthria, dysphagia, loss of gag reflex

Spinal V- ipsilateral pain and temperature of face

Spinothalamic tract: CONTRA pain/temperature of body

Descending hypothalamics: IPSI Horner syndrome

- vertigo
- diplopia
- nystagmus
- vomiting
- IPSI ataxia
Associated area/deficit for:

AICA
Lateral inferior pontine syndrome

Facial nucleus and fibers: IPSI facial paralysis, loss of anterior 2/3 taste, lacrimation, salivation and corneal reflex, hyperacusis

Spinal trigeminal nucleus/tract: ipsilateral pain/temperature (face)

Contralateral pain/temperature loss body,

middle cerebellar peduncle: ipsilateral ataxia

vestibular nuclei: vertigo, nystagmus

Ipis horner's
Associated area/deficit for:

Posterior cerebral artery
(1)
- CONTRA homonymous hemianopia with macular sparing
- supplies occipital cortex
Associated area/deficit for:

Middle cerebral artery
(3)
- CONTRA face and arm paralysis and sensory loss
- aphasia (dominant sphere)
- left-sided neglect (nondominant lesion)
Associated area/deficit for:

Anterior cerebral artery
(2)
- supplies medial surface of the brain
- leg-foot area of motor and sensory cortices
Associated area/deficit for:

Anterior communicating artery
(1)
- lesion may cause visual field defects
What is the most common site of circle of Willis aneurysms?
Anterior communicating artery
Associated area/deficit for:

Posterior communicating artery
(3)
- common area of aneurysm

- causes CN III palsy - "down and out"
Associated area/deficit for:

Lateral striate
(4)
- divisions of middle cerebral artery

Supplies:
- internal capsule
- caudate
- putamen
- globus pallidus

"Arteries of Stroke"
An infarct of the posterior limb of the internal capsule causes what?
- pure motor hemiparesis
Associated area/deficit for:

Watershed zones
(2)
Between:
- anterior cerebral / middle cerebral
- posterior cerebral / middle cerebral
Damage to watershed zones in severe hypotension leads to?
- upper leg / upper arm weakness
- defects in higher-order visual processing
Associated area/deficit for:

Basilar artery
(1)
- infarct causees "locked-in syndrome"
- CN III is typically intact
Associated area/deficit for:

in general, stroke of anterior circle
(2)
- general sensory and motor dysfunction
- aphasia
Associated area/deficit for:

in general, stroke of posterior circle
(4)
Cranial nerve deficits
- vertigo
- visual deficits

- coma
- cerebellar deficits (ataxia)

- Dominant hemisphere --> ataxia
- Nondominant hemisphere --> neglect
Where do Berry aneurysms occur?
- at the bifurcations in the circle of Willis
Most common site of Berry aneurysms?
- the bifurcation of the anterior communicating artery
Most common complication of Berry aneurysms and what that leads to?
- Rupture --> leads to hemorrhagic stroke/subarachnoid hemorrhage
What diseases/syndromes are Berry aneurysms associated with?
(3)
- adult polycystic kidney disease
- Ehlers-Danlos syndrome
- Marfan's syndrome
Other risk factors for Berry aneurysms?
(4)
- advanced age
- HTN
- smoking
- race (higher risk in blacks)
What are Charcot-Bouchard microaneurysms associated with?
- chronic HTN
What do Charcot-Bouchard microaneurysms affect?
- small vessels (ie. in basal ganglia, thalamus)
Epidural hematoma
rupture of midle meningeal artery, often 2ndary to fracture of temporal bone
*lucid interval"

rapid expansion -> transtentorial herniation

CNIII palsy


CT shows "biconvex disk" not crossing duture lines, flax, tentorium
Subdural hematoma
rupture of bridging veins-> slow venous bleeding

seen in elderly individuals, alcoholics, blunt trauma, shaken baby (brain atrophy, shaking, whiplash)

crescent shaped hemorrhage that crosses suture lines, midline shift, gyri preserved, does not cross flax, tentorium
Subarachnoid hemorrhage
rupture of aneurysm (Berry), or AVM
rapid time course, "worse headache of my life"

bloody or yellow spinal tap

2-3 days afterward has risk of vasospasm due to blood breakdown (treat with nimodipine), and rebleed -> ischemia
Intraparenchymal (HTNsive) hemorrhage
most often systemic HTN, but also amyyloid angiopathy (Alzheimer's), vasculitis (DM), and neoplasm

typically in basal ganglia and internal capsule
Ischemic brain disease
irreversible damage after 5 minutes - most vulnerable hippocampus, neocortex, cerebellum, *watershed areas*
Atherosclerosis in ischemic brain disease
thrombi lead to ischemic stroke -> subsequent necrosis

cystic cavity with reactive gliosis
Hemorrhagic stroke in ischemic brain disease
intracerebral bleeding, often due to HTN, anticoagulation and cancer
2ndary to ischemic stroke: reperfusion of ischemic/damaged vessels
Ischemic stroke
emboli block large vessels, etiologies include A fib, carotid dissection, patent foraen ovale, endocarditis

lacunar strokes block small vessels, may be sndary to HTN

tPA within 4.5 hours
Transient ischemic attack
brief, reversible episode of neurologic dysfunction lasting fewer than 24 hours
Dural venous sinuses
cerebral veins -> venous sinuses -> internal jugular vein
Ventricular system
CSF made by choroid plexus, reabsorbed by venous sinus arachnoid granulations

lateral ventricles -> foramen of Monro/ventricular Foramen -> third ventricle -> cerebral aqueduct -> 4th ventricle -> subachnoid space (Lateral Foramina of Luschka, Medial foramen of Magendie)
Normal pressure hydrocephalus
Dementia, ataxia and urinary incontinence "Wet, wobbly, and wacky"
reversible cause of dementia in elderly

Increases subarachnoid volume but not CSF pressure-> distortion of corona radiata
Communicating hydrocephalus
decreased CSF reabsorption by arachnoid villi -> increased intracranial pressure, papilledema, herniation
Obstructive (noncommunicating) hydrocephalus
caused by a structural blockage of CSF circulation
Hydrocephalus ex vacuo
increase of CSF due to atrophy without an increase in pressure/damage
Spinal nerves
8 cervical, 12 thoracic, 5 lumbar, 5 sacral, 1 coccygeal

Nerves C1-C7 exit above corresponding vertebra - all others below
Dorsal column
ascending pathway for fine touch, proprioception, vibration, pressure

receptor from body -> neuron body in DRG -> travels ipsilateral until synapsing in lower medulla -> decussates as internal arcuate fibers -> ascends as medial lemniscus -> synapses in VPL of thalamus -> 3rd order neuron goes to somatosensory cortex

Gracile fasciculus from lower extremities to gracile nucleus
Cuneate fasciculus from upper extremities to cuneate nucleus

ordered as you are with hands at sides -arms on outside, legs inside
Lesions in dorsal column
in spinal cord -> ipsilateral loss of function

above decussation (medulla) -> contralateral
Anterolateral/spinothalamic tract
ascending pathway for pain and temperature

1st neuron has cell body in DRG -> synapses in dorsal horn of spinal cord -> 2nd neuron immediately decussates -> ascends in lateral spinothalamic tract -> synapses in VPL -> 3rd neuron -> somatosensory cortex

Legs are lateral
Lesions in anterolateral/spinothalamic tract
contralateral loss of function
Lateral corticospinal tract
descending voluntary movement

Cortex -> posterior limb of internal capsule -> crus cerebri (midbrain) -> base of pons -> pyramids (medulla) -> pyramidal decussation -> lateral spinal corticospial tract -> ventral horn synapse -> muscle

cortex -> ventral horn = upper motor neuron
ventral horn -> muscle = lower motor neuron
Upper motor neuron lesion
everything is turned up

spastic paralysis, increased muscle tone, diuse atrophy, hyperreflexia, Babinski (toes go UP), clasp knife spasticity
Lower motor neuron lesions
everything is lowered

flaccid paralysis, hypotonia, muscle atrophy, hyporeflexia, no Babinski
Poliomyelitis
caused by polio virus -> oropharynx/small intestine symptoms -> travel to anterior horn of spinal cord -> LMN destruction

symptoms: malaise, headache, fever, nausea, abdominal pain, sore throat, LMN lesions

CSF with lymphocytic pleocytosis with slightly elevated protein, no change in glucose

virus present in stool/throat
Werdnig-hoffman disease
infantile spinal muscular atrophy: "floppy baby," tongue fasciculations, median death at 7 months

degeneration of anterior horns, LMN involvement
AR
Amyotrophic lateral sclerosis
both LMN and UMN signs; no sensory, cognitive, or oculomotor deficits

presents as fasciculations-> atrophy; progressive and fatal

can be caused by superoxide dismutase 1 defect

Riluzole can lengthen survival by decreasing presynaptic glutamate release
Tabes dorsalis
degeneration of dorsal columns and dorsal roots due to tertiary syphilis -> impaired proprioception and locomotor ataxia

Charcot's joints, shooting pain, Argyll Robertson pupil, absent DTRs, positive Pomberg, sensory ataxia at night (dark)
Friedreich's ataxia
AR trinucleotide repeat: GAA -> frataxin (mitochondria function)

staggering gait, frequent falling, nystagmus, dysarthria, pes cavus, hammer toes, hypertrophic cardiomyopathy (death)

kids with kyphoscoliosis

Friedreich is Fratastic, he pledged GAA and is always stumbling, staggering, falling
Brown-Sequard Syndrome
hemisection of spinal cord

1. ipsilateral UMN signs below lesion (corticospinal tract)
2. Ipsilateral fine touch, vivration, proprioception below lesion (dorsal column)
3. contra pain and temperature loss below (spinothalamic tract)
4. Ipsilateral loss of all sensation at level
5. LMN signs at level of lesion
Horner's syndrome
1. Ptosis (superior tarsal muscle) 2. Anhidrosis 3. Miosis
loss of sympathetic innervation

Pathway: hypothalamus -> intermediolateral column 0> superior cervical ganglion -> pupil, smooth muscle of eyelids, sweat glands
Reflexes
Biceps = C5
Triceps = C7
Patella = L4
Achilles = S1
Mororeflex
"hang on for life" abduct/extend limbs when startled then draw together - normal disappear with 1st year
Rooting reflex
movement of head toward one side if cheek or mouth stroked (nipple seeking)
Sucking reflex
sucking response when roof of mouth is touched
Palmar reflex
curling of fingers when palm stroked
Babinski reflex
dorsiflexion of large toe and fanning of other toes with plantar reflex

up with UMN lesion
Gallant reflex
stroking one side of the spine while newborn in ventral suspension causes lateral flexion of lower body towards stimulated side
Pineal gland
melatonin secretion - circadian rhythms
Superior colliculi
conjugate vertical gaze center

lesion cause Parinaud syndrome - paralysis of conjugated gaze, can be due to pinealoma
Inferior colliculi
auditory
Cranial nerves
On Old Olympus's Towering Tops A Finn And German Viewed Some Hops


Olfactory, Optic, Oculomotor, Trochlear, Trigeminal, Abducens, Facial, Auditory vestibular (vestibulocochlear) Glossopharyngeal, Vagus, (Spinal) Accessory, Hypoglossal
CN I
olfactory nerve- smell
projections through cribriform plate
CN II
optic nerve
sight
exits through optic canal
CN III
Eye movements (SR, IR, MR, IO), pupillary constriction (PS: E-W nucleus, muscarinic R). accommodation, eyelid opening
exits through superior orbital fissure
CN IV
eye movement (SO)- downward gaze when eye is fully adducted (looking at nose)
exits through superior orbital fissure
CN V
Trigeminal

mastication, facial sensation (opthalmic, maxillary, mandibular division)
V1 branch exits through superior orbital fissure
V2 exits through foramen rotundum
V3; foramen ovale
CN VI
Eye movement (LR)
exits through superior robital fissure
CN VII
Facial nerve

facial movement, taste anterior 2/3 tongue, lacrimation, salivation, eyelid closing, stapedius muscle in ear (dampens sound)
exits through auditory canal (stylomastoid foramen)
CN VIII
vestibulocochlear

hearing and balance

exits through auditory canal
CN IX
glossopharyngeal
taste from posterior 1/3 tongue, swallowing, salivation (parotid), carotid body and sinus chemo/baroreceptors, and stylopharyngeus (elevates pharynx, larynx)

exits through jugular foramen
CN X
vagus
swallowing, palate elevation, midline uvula, talking, coughing, thoracoabdominal viscera, arotic arch chemo/baroreceptors
exits through jugular foramen
CN XI
spinal accessory nerve
head turning, shoulder shrugging

exits through jugular foramen (enters skull through foramen magnum)
CN XII
hypoglossal
tongue movement
exits through hypoglossal foramen (canal)
Cranial nerve nuclei in midbrain
CN III, IV
Cranial nerves nuclei in pons
CN V, VI, VII, VIII
Cranial nerve nuclei in pmedulla
CN IX, X, XI, XII
Corneal reflex
afferent V1 ophthalmic (nasociliary branch)
efferent VII (temporal branch : orbicularis oculi)
Lacrimation reflex
afferent V1, efferent VII
Jaw jerk reflex
V3 sensory from masseter
V3 motor to masseter
Pupillary reflex
afferent II, efferent III
Gag reflex
afferent IX, efferent IX, X
Vagal nucleus Solitarius
visceral sensory information (taste, baroreceptors, gut distention) for CN VII, IX, X
Vagal nucleus ambiguus
motor innervation of pharynx, larynx and upper esophagus, CN IX, X, XI
Vagal dorsal motor nucleus
parasympathetic fibers to heart, lungs, and upper GI
Optic canal
CN II, ophthalmic artery, central retinal vein
Superior orbital fissure
CN III, IV, V1, VI, ophthalmic vein, sympathetic fibers
Foramen rotundum
CN V2
Foramen Ovale
CN V3
Foramen spinosum
middle meningeal artery
internal auditory meatus
CN VII, VIII
jugular foramen
CN IX, X, XI, jugular vein
Hypoglossal canal
CN XII
Foramen magnum
spinal roots CN XI, brain stem, vertebral arteries
Cavernous sinus
venous sinuses on either side of pituitary
blood from eye and superficial cortex -> cavernous sinus -> internal jugular vein

CN III, IV, V1, V2, and VI, and postganglionic sympathetic fibers to the orbit all pass through here

cavernous portion of internal carotid artery is also here
Cavernous sinus syndrome
ophthalmoplegia, ophthalmic and maxillary sensory loss
Danger triangle of face
edges of mouth to bridge of nose

potential for an infection to spread from here (ex. upper lip) to the brain via venous drainage
facial vein -> ophthalmic veins -> cavernous sinus
CN XII LMN lesion
tongue deviated towards side of lesion due to weakened muscles on affected side
CN V motor lesion
jaw deviates toward side of lesion due to unopposed force from opposite pterygoid muscle
CN X lesion
uvula deviates away from side of lesion - weak side collapse and uvula pulled away
CN XI lesions
weakness of turning head to contralateral side, shoulder droop on same side
Conductive hearing loss
abnormal Rinnne test (bone > air); Weber localizes to affected ear
Sensorineual hearing loss
normal Rinne test (air > bone); Weber test localizes to unaffected ear
Facial nerve UMN lesion
motor cortex or connection between cortex and facial nucleus
contralateral paralysis of lower face only; bilateral UMN innnervation of upper face
Facial nerve LMN lesion
Ipsilateral paralysis of upper and lower face
Bell's palsy
complete destruction of facial nucleus itself or its brachial efferent fibers

peripheral ipsilateral facial paralysis with inability to close eye on involved side

idiopathic -most recover
other causes: AIDS, Lyme disease, HSV, Sarcoidosis, Tumors, Diabetes
Muscles of mastication
3 muscles close: masseter, temporalis, medial pterygoid
1 opens: lateral pterygoid
all are innervated by trigeminal nerve V3
Retinitis
retinal necrosis + edema = atrophic scar
associated with CMV in AIDS patients
Iritis
due to systemic inflammation
Near vision
ciliary muscle contracts (zonular gibers relax -> lens relaxes -> more convex)
can't see far away
Distant vision
ciliary muscle relaxes (lens flattens)
can't see up close
Aging of eye
sclerosis and decreasing elasticity causes presbyopisa (no near vision)
Retinal artery occlusion
acute painless monocular loss of vision, pale retina and cherry-red macula (own blood supply -choroid artery)
Open/wide angle glaucoma
obstructed outflow (eg. Canal of Schlemm); myopia, increases with aging, African-American race
most often "silent" painless
Closed/narrow angle glaucoma
contact between lens and central iris forms seal - flow of normal fluid behind pupil messed up
very painful, impaired vision, rock-hard eye, frontal headache, ophthalmologic emergency
do not give epinephrine
Cataract
painless, bilateral opacification of lens - impaired vision

risk: age, smoking, EtOH, sunlight, classic galactosemia, galactokinase deficiency, DM, trauma, infection, steroids
Papilledema
increased intracranial pressure -> elevated optic disk with blurred margins-> blind spot
Pupillary constriction
pupillary spincter muscle (circular muscle), parasympathetic
CN III from Edinger-Westphal nucleus -> ciliary ganglion
Pupillary dilation
radial muscle (pupillary dilater muscle), sympathetic
T1 preganglionic sympathetic -> superior cervical ganglion -> postganglionic sympathetic -> long ciliary nerve
Pupillary light reflex
retina -> CN II -> pretectal nuclei in midbrain -> bilateral activation of E-W nucleui -> pupils contract bilaterally

Marcus gun pupil -> afferent pupillary defect -> decreased bilateral constriction when shone light in affected eye
Retinal detachment
separation of neursensory layer of retina from pigment epithelium -> degeneration of photoreceptors -> vision loss
Age-related macular degeneration
loss of central vision (scotomas)
dry/atrophic is slow. due to fat deposits
wet is rapid, due to neovascularization
Right anopia
lesion in optic nerve before optic chiasm
bitemporal hemianopia
lesion/compression in optic chiasm
located near pituitary gland, often from tumor
Contralateral homonymous hemianopia
lesions of optic tracts, can occur after optic chiasm, both temporal and parietal optic radiations, lateral geniculate nucleus
uncommon
Contralateral superior quantrantopia
"pie in the sky"
temporal lobe lesions often from MCA inferior division infarct interrupting lower optic radiations through temporal lobe, lower bank of calcarine fissure
Contralateral inferior quantrantopia
"pie on the floor"
MCA superior lesion infarct in the parietal lobe takes out upper optic radiations
PCA infarct takes out primary visual cortex, upper calcarine bank
Macular sparing
it's a thing
Meyer's loop
inferior retina -> loops around inferior horn of lateral ventricle
dorsal optic radiation - superior retina, takes shortest path via internal capsule
Internuclear ophthalmoplegia
lesion in medial longitudinal fasciculus -> medial rectus palsy on attempted lateral gaze
nystagmus in abducting eye
convergence normal
seen commonly in MS
Dementia
a decline in cognitive ability, memory, or function with intact consciousness
Alzheimer's disease
most common cause of dementia in elderly, Down's syndrome patients have increased risk

Familial form (10%)
early onset: APP (on chromosome 21), presenilin-1 (14), presenilin-2 (1)
later onset: ApoE4 (19)

ApoE2 is protective

widespread cortical atrophy: decreased ACh
senile plaques: extracellular beta-amyloid core, amyloid angiopathy -> intracranial hemorrhage
neurofibrillary tangles: intracellular, abnormally phosphorylated tau protein = insoluble cytoskeletal elements, correlate with degree of dementia
Pick's disease
frontotemporal dementia: dementia, aphasia, parkinsonian aspects, change in personality (temper, mean)
spares parietal lobe and posterior 2/3 superior temporal gyrus

Pick bodies: intracellular, aggregated tau protein
frontotemporal atrophy
Lewy body dementia
Parkinsonism with dementia and hallucinations
alpha-synuclein defect
Creutzfeldt-jakob disease
rapidly prgressive (weeks to months) dementia with myoclonus
spongiform cortex
prions -PrPc -> PrPsc sheet resistant to proteases
Multiple sclerosis
autoimmune inflammation and demyelination of CNS, optic neuritis; relapsing/remitting neuro symptoms separated by time and location

increased IgG protein in CSD, oligoclonal bands are diagnostic
MRi shoes periventricular plaques

ts: beta-interferon, immunosuppression, symptomatic
Guillain-Barre syndrome
bilateral ascending muscle weakness, facial paralysis in 50% of cases, autonomic function can be compromised

majority of patients recover completely after weeks to months

associated with infections -> autoimmune attack of peripheral myeline due to molecular mimicry: C. jejuni, herpesvirus, inoculations and stress

increased CSF protein with normal cell count

tx: respiratory support, plasmapheresis, IV IG
Progressive multifocal leukoencephalopathy
demyelination of CNS due to destruction of oligodendrocyte-> rapidly progressive, often fatal

associated with JC virus in AIDS patients
Acute disseminated encephalomyelitis
multifocal perivenular inflammation and demyelination after infection (chickenpox, measles) or certain vaccinations (rabies, smallpox)
Metachromatic leukdystrophy
AR lysosmal storage disease, most commonly arylsulfatase A deficiency, build up of sulfatides leads to impaired production of myelin sheath

ataxia, dementia
Charcot-Maire-Tooth disease
hereditary motor and sensory neuropathy: defective production of proteins invovled in structure and function or peripheral nerves or the myelin sheath
Partial seizures
localized to 1 area of the brain, most often from medial temporal lobe, ex. will just have one arm spasm
often has aura (smells, vision changes)
can secondarily generalize

simple partial - conciousness intact: motor, sensory, autonomic, psychic
complex partial (impaired consciousness)
Generalized seizures
more common than partial
1. absence - no postictal confusion, blank stare for a few seconds
2. Myoclonic - quick, repetitive jerks
3. tonic-clonic - alternating stiffening movement
4. tonic - stiffening
5. Atonic - "drop" seizures, commonly mistaken for fainting
Status epilepticus
recurring seizures without restoration of consciousness

requires benzodiazepines emergently then antiepileptics
Causes of seizures in children
genetic, infection (febrile), trauma, congenital, metabolic
Causes of seizures in adults
tumors, trauma, stroke, infection
Causes of seizures in elderly
stroke, tumor, trauma, metabolic, infection
Treatment of seizures for pregnant women
phenobarbital
Migraine
unilateral heache, 4-72 hours, pulsating pain with nausea, photophobia, phonophobia, +/- aura

irritation of CN V and release of substance P, GCRP, vasoactive peptides

tx: propranolo, NSAIDs, sumatriptan for acute migraines
Tension headache
unilateral; repetitive brief headaches, no photphobia, phonophobia, aura
Cluster headaches
unilateral, repetitive brief headaches, characterized by periorbital pain, ipsilateral lacrimation, rhinorrhea, Horners syndrome

males>>females

tx: inhaled O2, sumatriptan
Vertigo
illusion of movement,
peripheral- more common, inner ear etiology, postitional testing shows delayed horizontal nystagmus

central vertigo - brain stem or cerebellar lesion, positional testing shows immediate nystagmus in any direction, may change directions
Meniere's diseae
abrupt recurrent attacks of vertigo with deafness or tinnitus, unilateral, N/V
Sturge-Weber syndrome
congenital disorder with port-wine stains, typically in V1 ophthalmic distribution, ipsilateral leptomenigeal angiomas, pheochromocytomas

can cause glaucoma, seizures, hemiparesis, mental retardation

occurs sporadically
Tuberous sclerosis
HAMARTOMAS: hamartomas in CNS and skin, Adenoma sebaceum (cutaneous angiofibromas), Mitral Regurg, Ash-leaf spots, cardiac Rhabdomyoma, Tuberous sclerosis, autosomal dOminant, Mental retardation, renal Angiomyolipoa, Seizures
Neurofibromatosis type I
cafe-au-lait spots, Lisch nodules (pigmented iris hamartomase), neurofibromas in skin, optic gliomas, pheochromocytomas
AD with 100% penetrance but variable expression

mutated NF-1 gene on chromosome 17 (negatively regulates RAS pathway)
von Hippel-Lindau disease
cavernous hemangiomas in skin, mucosa, organs, bilateral renal cell carcinoma, hemangioblastoma in retina, brain stem, cerebellum, pheochromocytomas

AD, mutated tumor suppresor CHL on Chr3
Majority of adult primary tumors are ____
supratentorial
Majority of adult primary tumors are ____
infratentorial

infant-tentorial
Most common type of brain tumor
metastases: well circumscribed, present at gray-white junction
Glioblastoma
most common primary brain tumor with poor prognosis <1 yrs

cerebral hemispheres can cross corpus callosum

astrocytes stain for GFAP

"pseudopalisading" pleomorphic tumor cells, borer central areas of necrosis and hemorrhage
Meningioma
second most common primary brain tumor

often occurs in convexities of hemispheres and parasagittal region

arises from arachnoid cells external to brain

usually benign and resectable

plindeled cells concentrically arranged in a whorled pattern, psammoma bodies (laminated calcifications)
Schwannoma
Schwann cell origin
often localized to CN VIII, cerebellopontine angle
resectable,
S-100 positive

bilateral in NF-2
Oligodendroglioma
relatively rare, slow growing
most often in frontal lobes -> personality changes, seizures, temper

chicken wire capillary pattern

oligodendroctyes: "fried egg" cells - round nuclei with clear cytoplasm

often calcified
pituitary adenoma
most commonly prolactinoma; bitemporal hemianopia

hyper/hypopituitarism
Pilocytic astrocytoma
low grade, well circumscribed, in kids

most often found in posterior fossa

may be supratentorial, GFAP positive

benign, good prognsis

Rosenthal fibers -eosinophilic, corkscrew fibers

cystic and solid
Medulloblastoma
kids: highly malignant cerebella tumor
form of primitive neuroectodermal tumor
can compress 4th ventricle

small blue cells, radiosensitive, homer-wright rosettes
Ependymoma
kids: ependymal cell tumors most often in 4th ventricle

poor prognosis, kids

characteristic perivascular pseudorosettes, rod-shaped blepharoplasts (basal ciliary bodies) found near nucleus
Hemangioblastoma
kids

most often cerebellar, assoicated with von H-L syndrome when with retinal ngiomas

can produce EPO -> polycythemia

foamy cells and high vascularity
Craniopharyngioma
kids
benign, confused with pituitary adenoma
most common childhood supratentorial tumor

remnants of Rathke's pouch, tooth enamle-like calcifications
Uncal herniation
ipsilateral dilated pupils/ptosis - stretching of CNIII
contralateral homonymous hemianopia - compression of ipsilateral cerebral artery
ipsilateral paresis- compression of contralateral crus cerebria (Kernohan's notch)
Duret hemorrhages - paramedian artery rupture - caudal displacement of brain stem
Ring-enhancing lesions
metastases (lung>breast>kidney>melanoma>GI), abscesses, toxoplamosis, primary CNS lymphoma
Uniformly enhancing lesions
metastaic lymphoma, meningioma, mets
Heterogeneously enhancing lesion
glioblastoma multiforme