Neurology Flashcards
What type of neuronal cell has a different embryonic origin than the rest?
Microglia - from mesoderm; CNS macrophage
Others are from neuroectoderm
Stains for different cells?
Nissl substance = dendrites, cell bodies (RER) - NOT axons
GFAP = astrocytes
Blood Brain Barrier
- tight junctions nonfenestrated endothelial cells
- BM
- astrocyte foot process
Lipids get through
Glucose/AA need carriers
NOT present in area postrema and neurohypophysis
Lateral Area Hypo
Hunger
Inhibited by Leptin
Destruction: anorexia, FTT
Ventromedial Area Hypo
Satiety
Stimulated by Leptin
Destruction: obesity, hyperphagia
Anterior Hypothalamus
Cooling, PNS
“Anterior nucleus = A/C”
Posterior Hypothalamus
Heating, Symp
Suprachiasmatic Nucleus
Circadian Rhythm
Stimulates pineal gland -> melatonin
Preoptic Area Hypothalamus
GnRH
Dorsomedial Nucleus
Stimulates GI - savage behavior, obesity
Arcuate Nucleus
Dopamine
GHRH
Supraoptic Nucleus
ADH
Paraventricular Nucleus
Oxytocin
Stages of Sleep and EEG waveform
“BATS Drink Blood”
Awake (open eyes) = beta (highest freq, lowest amp)
Awake (closed eyes) = alpha
N1 light sleep = theta
N2 deeper sleep; bruxism = sleep spindle, K complexes
N3 deepest/slow wave sleep = delta (lowest freq, highest amp)
REM = beta
What stage of sleep associated with night terrors, sleep walking, bedwetting? What drugs treat?
N3
EtOH, Benzo, Barb = decreased REM and delta sleep
Bedwetting = DDAVP
What happens during REM sleep?
loss of motor tone variable pulse, BP dreaming penil/clitoral tumescence memory processing
What characterizes narcolepsy? What stage? Tx?
Awake -> REM sleep:
- excessive daytime sleepiness
- cataplexy
- HypnoGOgic (going to sleep); HypnoPOmpic (post sleep) hallucinations
Tx:
- stimulants: amphetamine, modafinil
- PM sodium oxybate GHB
Changes in sleep stages in depression?
- dec. slow wave N3 deep sleep
- inc. total REM
- rpted PM awakenings
- early AM awakening
Kallman Syndrome?
Dec. GnRH (Hypogonadism) + Anosmia
Corneal & Lacrimation Reflex
CN V1
CN VII
Jaw Jerk Reflex CN
V3
Pupillary Reflex CN
CN II
CN III
Gag Reflex CN
CN IX
CN X
Mnemonic for S vs. M in CN?
Some Say Marry Money But My Brother Says Big Brains Mean More
CN Pathway
1 Cribiform Plate 2 Optic Canal 3, 4, 6, V1 Superior Orbital Fissure V2 Foramen Rotundum V3 Foramen Ovale 7, 8 Internal Auditory Meatus 9, 10, 11 Jugular Foramen 12 Hypoglossal Canal
Foramen Magnum = spinal roots of Cn XI, Brain stem, VA
V = Standing Room Only
Damage to CN III vs. IV vs. VI?
CN III: “Down and out,” ptosis, mydriasis, loss of accommodation
CN IV:
- eye moves upward
- esp with contralateral gaze
- compensatory head tilt TOWARD side of the lesion
CN VI:
- medial eye, can’t abduct
- Obliques move the eye in the Opposite direction”
Afferent vs. Efferent Pupillary Eye Defect?
Afferent = Marcus Gunn Pupil = Optic N. damage
- affected eye: nothing constricts with light
- unaffected eye: both will constrict with light
Efferent = Oculomotor N.
- affected eye UNABLE to constrict with light in EITHER eye
Meyer vs. Dorsal Optic Radiation?
Meyer = temporal loop
Dorsal Optic = parietal loop
Forebrain (Prosencephalon)
Telencephalon = Cerebral Hemispheres; Lateral ventricles Diencephalon = Thalamus; 3rd ventricle
Midbrain (Mesencephalon)
Mesencephalon = Midbrain; aqueduct
Hindbrain (Rhomboencephalon)
Metencephalon = Pons, Cerebellum, upper 4th ventricle Myelencephalon = Medulla, lower 4th ventricle
Screening for NT defects
When do neuropores normally fuse?
Elevated AFP in maternal serum or amniotic fluid
4th week
Spina Bifida Occulta vs. Meningocele vs. Myelomeningocele
Spina Bifida Occulta - opening in bone spinal canal, tuft hair/dimple, nl AFP
Meningocele - meninges out
Myelomeningocele - meninges + spinal cord out
Anencephaly associated with what condition?
Failure of anterior NT to close - inc. AFP
Polyhydramnios (no swallowing center)
Holoprosencephaly due to what?
Failure of L and R hemispheres to fuse.
Sonic Hedgehog Pathway
Midline deformities - cleft lip/palate, cyclopia
Chiari I vs. II
I = tonsils -> syringomyelia II = vermis & tonsils -> hydrocephalus, assoc. myelomeningocele
Dandy-Walker
Agenesis of cerebellar vermis
Enlargement of 4th ventricle (to fill posterior fossa)
-> Hydrocephalus
-> Assoc. spina bifida
Jaw, Uvula, Tongue, Neck Deviate towards or away lesion?
Tongue = Towards "licking the lesion" CN XII Uvula = Away - good side works CN X Jaw = Towards CN V3 Neck = Weakness turning head towards CONTRALAT side of lesion. (SCM). Droop of ipsilateral shoulder (Trapezius) CN XI
Kluver-Bucy
hyperorality
hypersexuality
disinhibition
Bilateral Amygdala
Right Parietal-Temporal (non-dom)
Hemineglect
Left Parietal-Temporal (dom)
Gerstmann Syndrome
- agraphia
- acalculia
- finger agnosia
- L and R disorientation
Mammillary Bodies - lesion leads to?
Wernicke-Korsakoff
- ataxia, confusion
- opthalmoplegia, CN VI palsy
- memory loss, confabulation
CAN of beer = confusion, ataxia, nystagmus
Give thiamine!
Cerebellar vermis vs. cerebellar hemisphere lesions?
IPSILATERAL defects
Hemisphere = “Hemispheres are lateral, affect lateral limbs”
- lateral limb ataxia
- intention tremor
- fall TOWARD side of lesion
Vermis = “Vermis is centrally located; affect central body”
- truncal ataxia
- dysarthria
Subthalamic Nucleus lesion?
Hemiballismus
PPRF vs. Frontal eye field lesions?
PPRF: AWAY from side of lesion
Frontal Eye Field: TOWARD lesion
Superior Colliculi lesion?
Paralysis of upward gaze (Parinaud’s Syndrome)
Central Pontine Myelinolysis causes?
Locked In Syndrome
Correct HypoNa too fast
“If you go from low to high, your pons will die”
“If you go from high to low, your brain will blow”
Broca vs. Wernicke vs. Conduction
Broca = expressive aphasia Wernicke = comprehensive aphasia Conduction = can't repeat; arcuate fasiculus
Cavernous Sinus Structures
CN 3, 4, 6, V1, V2
Internal Carotid
Internal Jugular Vein
Weber Syndrome?
Midbrain Infarction - PCA
- CN III palsy
- contralateral spastic hemiparesis (cerebellar peduncle)
What artery supplies the pons?
AICA
Medial Inferior vs. Lateral Pons
Medial Inferior
- Motor - contralateral
- ML - DC contralateral
- PPRF - gaze towards side of lesion
- CN VI
Lateral: 4 “S” + 7,8
- spinocerebellar - ipsi
- spinothalamic - ALS contra
- sympathetic - ipsi Horners
- sensory nuclei of V
- CN VII
- CN VIII
“Facial droop = AICA’s pooped”
4 Ms and 4 S of brainstem lesions?
M:
- Motor
- ML
- MLF
- Motor CN
S:
- spinocerebellar - ipsi
- spinothalamic - ALS contra
- sympathetic - ipsi Horners
- sensory nuclei of V
Wallenberg Syndrome?
Lateral Medulla - PICA
4 S + Nucleus Ambiguus + - hoarseness - dysphagia CN VIII - n/v, vertigo, ataxia
Medial Medulla Syndrome?
ASA
- Motor, ML
- CN XII
Acom vs. Pcom presentation?
Both are usually saccular aneurysm
ACom = Bitemporal Hemianopsia PCom = CN III palsy
Right INO sx
MLF - coordinates abducens with CN III to move eyes in same direction
Right INO = Right MLF messed up
On leftward gaze,
- R eye can’t adduct
- L eye nystagmus
“MLF in MS”
Areas of brain most vulnerable to ischemic stroke? What about hemorrhagic stroke?
Ischemic: Hippocampus Neocortex Cerebellum Watershed!
“ischemic HYPOxia - “HIPPOcampus” most vulnerable
Hemorrhagic:
Basal Ganglia
Imaging type to show changes in ischemic stroke earliest?
Diffusion Weighted MRI: bright
Note: NCHCT: dark
Communicating vs. Noncommunicating Hydrocephalus? Sx?
Communicating = dec. CSF absorption Noncommunicating = structural blockage
H/A, papeilledema, uncal herniation - CN III palsy, death
NPH
“wet, wobbly, wacky”
Triptan - MOA, Toxicity?
Serotonin agonist - inhibits CN V activation, vasoconstrict
Toxicity: coronary vasospasm (contraindicated in CAD, Prinzmetal angina)
Acronym for Brain Tumors: Adult vs. Child
Adult: MGM Studios:
Metastatic, GBM, Meningioma, Schwannoma
Child: Animal Kingdom, Magic Kingdom, Epcot:
Pilocytic Astrocytoma, Medulloblastoma, Ependymoma
Histologic Features of Adult Brain Tumors
GBM (Malig, Astrocytoma IV): pseudopalisading, GFAP
Meningioma (Benign): dural tail, whorled pattern, psamomma bodies
Schwannoma: S-100(+), cerebellarpontine angle
Hemangioblastoma: thin-walled capillaries, with minimal interweaving parenchyma
Oligodendroma = fried egg
Hemangioblastoma associated what condition?
von Hippel Lindau:
- hemangioblastoma - CNS, retina
- erythropoietin -> polycythemia
- renal cell carcinoma
Histologic Features of Child Brain Tumors
Pilocytic Astrocytoma: GFAP, Rosenthal fibers (corkscrew eosinophilic)
Medulloblastoma: Homer-Wright Rosettes (rosettes around just fibers)
Ependymoma: Perivascular Rosettes (rosettes around capillary
Craniopharyngioma: Calcifications
Uncal Herniation Features
Uncus = medial temporal lobe
- CN III - down and out
- ipsi PCA - contralat homonymous hemianopsia
- contral cerebral peduncle = ipsilateral paralysis
IV Benzo used for anesthesia?
Thiopental
IV Benzo used for anesthesia?
Midazolam
Toxic effect of inhaled anesthetics?
Malignant Hyperthermia (All except NO)
Halothane is Hepatotoxic
What anesthetic can cause dissociation, disorientation, hallucination?
Ketamine
Why shouldn’t we keep someone in the ICU on propafol drip?
Rapid induction, but HIGH TAG content
Local Anesthetic: two organic molecule types?
- caine
Esters
Amides: two I’s
What do you give to enhance local anesthetics?
Epinephrine vasoconstrict
What situation would you probably need more local anesthetic?
infected (acidic) tissue - can’t get thru membrane as effectively since alkaline anesthetics will be charged
Toxicity of Local anesthetics?
CNS excitation, Arrhythmias
What are the two types of Neuromuscular blocking drugs?
- Depolarizing = Succinylcholine
- depolarizes, so Ach agonist but its sustained so no muscle contraction - Nondepolarizing = -curarine, curium
- competitive antagonist to Ach
Order of loss with local anesthetics
- pain
- temperature
- touch
- pressure
Small > Large
Myelinated > Non
How do you reverse nondepolarizing NM agents?
Neostigmine + Atropine (prevent Muscarinic effects like bradycardia)
Toxic Effects of Succinylcholine
HyperCa
HyperK
Malignant Hyperthermia
STURGE-weber
Sporadic; Stain - port wine Tram Track Ca Unilateral Retardation Glaucoma/GNAQ gene Epilepsy
Tuberous Sclerosis
HAMARTOMAS:
Hamartomas in CNS and skin Angiofibromas on the skin (reddish brown papules) MR Ash-leaf spots Rhabdomyoma cardiac (Tuberous Sclerosis) autosomal dOminant Mental Retardation Angiomyolipoma renal Seizures/Shagreen patches/SEGA
NF I
ADom: Chr 17
cafe au lait lisch nodules neurofibromas pseudoarthrosis meningioma, astrocytoma, glioma, pheo
vHL
autosomal dominant:
- cavernous hemangioma
- bilateral renal cell carcinoma
- hemangioblastoma
- pheo
vHL = tumor suppressor
NT - location of synthesis NE Dopa 5HT Ach GABA
NE - locus ceruleus (pons) Dopa - substantia nigra (midbrain) 5HT - raphe nucleus (pons, medulla, midbrain) Ach - Basal nucleus of Meynert GABA - nucleus accumbens