Neuro Flashcards

(194 cards)

1
Q

Benign brain tumor that pushes on the brain tissue without invading it. seen parasaggital or at edges

A

Meningioma

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2
Q

“fried-egg appearance”, can have calcifications

A

oligodendroglioma

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3
Q

perivascular rosettes, hydrocephalus, 4th ventricle

A

Ependymoma (ependymal cells line ventricles)

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4
Q

degeneration of anterior motor horn

A

Poliomyelitis or Werdnig Hoffman

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5
Q

Synringomyelia (anterior white commisure)

A

LMN sx i.e. weakness + loss of P/T from UE (because usually at c8-t1)

Can expand to hit Anterior motor horn, as well as lateral horn t1 (horners)

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6
Q

UMN and LMN signs

A

ALS

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7
Q

Hypertrophic cardiomyopathy + degen of several neural tracks

A

Friedreich ataxia

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8
Q

where do you do lumbar puncture

A

L4-L5. spinal cord stops at L2 but cauda equina til s2. subarachnoid space

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9
Q

most common cause of Subarachnoid Hemorrhage (bleed on bottom of the brain)

A

Rupture of berry aneurysm (anterior circle of willis –> ACom branch points)

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10
Q

why is a Berry aneurysm susceptible to rupture?

A

Lacks a media layer

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11
Q

whats the AFP level in neural tube defect

A

HIGH as a fuckin KITE

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12
Q

most common cause of hydrocephalus in new born

A

Cerebral aqueduct stenosis (blocks 3–>4)

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13
Q

Foramen of Monro

A

Lateral ventricles –> 3rd

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14
Q

4th ventricle through Foramen meagendie/luschka into:

A

subarachnoid space

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15
Q

Define dandy-walker formation

A

congenital failure of cerebrellar vermis –> presents with absent cerebrelleum and massively dilated 4th ventricle (posterior fossa)

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16
Q

massivelyd dilated 4th ventricle

A

Dandy walker formation

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17
Q

downward displacement of cerebellar vermis and tonsils through foramen magnum

A

Arnold Chiari (2)

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18
Q

name 3 common associations with Arnold-Chiari malformation (type 2)

A

(cerebellar herniation)

Hydrocephalus, Synringomyelia, Meningomyelocele

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19
Q

Cystic degeneration of the spinal cord

A

Syringomyelia

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20
Q

lose pain and temp in UE

A

Syringomyelia

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21
Q

Lateral horn of hypothalamospinal tract

A

Synringomyelia can expand and knock this out = horners (t1)

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22
Q

muscle atrophy and weakness in syringomyelia

A

expands to knock out Anterior Horn (LMNs)

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23
Q

Polio damages:

A

Anterior motor horn–> LMN signs

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24
Q

Floppy baby, autosomal recessive

A

Werdnig-Hoffman; degen of anterior motor horn

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25
ALS: Degen of ________
UMN and LMN of Corticospinal tract
26
Corticospinal tract is damaged in
ALS
27
Enzyme mutation that can cause ALS
Superoxide dismutase
28
_____ increases survival in ALS pt by ______
Riluzole ("Lou gehrigs") increases survival by decreasing presynaptic glutamate release
29
Glutamate antagonist
Riluzole used to treat ALS (Lou Gehrigs)
30
What are the neural components of Friedreich Ataxia
Degenerative disorder of the cerebellum: ataxia and Spinal cord: loss of MVP, deep tendon reflex, LE muscle strength
31
describe the frataxin gene (lost in freidreich)
Mitochondrial iron regulation...loss = iron buildup and thus free radical damage
32
first sign of friedreich ataxia
clumsyness
33
Neisseria menigitidis meningitis
through the NOSE nigga.
34
signs of meingitis
headache, nuchal rigidity, fever; Photophobia, vomiting, altered mental status.
35
where does lumbar puncture sample
Subarachnoid space
36
what ischemic neural effects can an Insulinoma have?
Repeated bouts of hypoglycemia --> global cerebral ischemia (brai needs glucose)
37
Pt has a stroke...whats the protocol for tx
give tPA--> have to do CT (noncontrast) to RULE OUT HEMORRHAGE!! tPA within 1st 4 hours aspirin/clopidogrel can be given to reduce risk
38
does TIA register on MIA?
Nope, its a reversible thang less than 15 minutes of focal neuro dysf(x)
39
hypoxia and irreversible damage
irreversible damage after 5 minutes of hypoxia. Hippocampus (pyramidal neurons/temporal lobe), Cerebral cortex (laminar necrosis layers 3 5 6) Cerebellum (purkinje layer)
40
hyaline arteriolosclerosis (HTN) leads to what type of stroke?
Lacunar stroke
41
Describe lacunar stroke
involves lenticulostriate vessels = small lacunar infarcts (cystic areas) Thalamus: pure sensory Internal capsule: pure motor
42
earliest change in ischemic stroke
Liquefactive necrosis 1st sign = red neuron = eosinophilic change of neuron cytoplasm
43
which cells are responsible for gliosis post storke
astrocytes
44
in stroke, neutrophils are day 1-3, which cell is day 4-7?
Microglia (MQ of the brain)
45
what are the 2 aneurysms in the brain?
Berry aneurysm (subarachnoid space) and Charcot-Bouchard (parenchymal space)
46
Describe charcot-bouchard aneurysm
due to HYPERTENSION. LENTICULOSTRIATE vessels going to BASAL GANGLIA (look in the center where the cord would attach) intracerebral hemorrhage/bleeding into PARENCHYMA (so not lobar)
47
sudden headache + nuchal rigidity
subarachnoid hemorrhage
48
LP indicating SAH
Xanthochromia (yellow due to bilirubin)
49
what does yellowish LP indicate
Subarachnoid Hemorrhage. Can be a bloody or yellowish tap = SAH
50
Berry aneurysm can cause
Bitemporal hemianopia by compressing optic chiasm Subarachnoid hemorrhage Hemorrhagic stroke
51
lens shaped lesion on CT
Epidural hematoma
52
lucid interval after bleed
Epidural hematoma
53
crescent shaped lesion on CT
subdural hematoma
54
Uncal herniation
1. CNIII: eye moves down and out + dilated pupil 2. PCA: contralat homonymous hemianopsia -- infarction of occipital lobe 3. Paramedian artery: Duret (brainstem) hem
55
deficiency of Arylsulfatase
``` Metachromatic Leukodystrophy (demyelination) -->sulfatides accumulate in lysosomes. ataxia/dementia ```
56
defeciency of galactocerebrosidase
Krabbe (buildup of galactocerebrosidase and psychosine). demyelination. Peripheral neuropathy, optic atrophy, developmental delay
57
Leukodystrophies (inherited mutations fuck up myelin)
AR: Metachromatic leukodystrophy (arylsulfatase) and Krabbe (galactocerebrosidase) X-linked: Adrenoleukodystrophy (long chain fatty acids--> brain and adrenals)
58
Clining features of MS
Blurred vision in one eye (optic nerve) vertigo and scanning speech (brainstem) internuclear opthalmoplegia (MLF) Hemiparesis (periventricular white matter) Bowel bladder and sexual dysfunction (ANS)
59
Lumbar puncture MS
Increased lymphocytes, increased Ig's with OLIGOCLONAL IgG bands on electrophoresis Myelin basic protein (because destroyed myelin)
60
Astrocytes
Neuroectoderm | GFAP = astrocyte marker
61
Microglia vs macroglia
Microglia: phagocytes. mesodermal Macroglia: astrocytes, oligo, ependymal. Neuroectoderm
62
Guillain Barre: injury to
schwann cells!!
63
Endoneural inflammation | endomysial inflammation
GBS | polymyositis
64
ADH and oxytocin synthesis
made in hypothalamus but stored in PP
65
Lateral hypothalamus
Lose lateral = lose weight
66
Ventromedial hypothalamus
Satiety. Lose ventromedial = verymuch hungry
67
Tau protein
Neurofibrillary tangle: Alzheimer | Round aggregates = pick bodies: Pick disease
68
Sx of Pick disease
Language (temporal) and behavior (frontal) deficits
69
Parkinsons, loss of ________ neurons in the _________ of the basal ganglia
dopaminergic | substantia nigra
70
Sx of Parkinsons
Tremor (pill rolling) at rest, disappears with movement Rigidity (cogwheel) in extremities Akinesia is slowing of voluntary movement Postural instability/shuffling gait
71
Expressionless face and tremor that disappears with movement
Parkinsons: Akinesia = expressionless face. Pill rolling tremor.
72
dementia in Parkinsons vs Lewy body
Lewy body: early dementia | Parkinsons: late dementia
73
Subtantia nigra vs caudate nucleus disorder
SN: Parkinsons (dopaminergic) CN: Huntington's (GABAergic. trinucleotide = anticipation)
74
When and why do you see Chorea (disorder)
See it in Huntingtons (loss of GABAergic neurons in caudate nucleus) Normally, GABA from BG to Cortex has an inhibitory hold on neurons. loss of GABA = random firing/movement = chorea
75
Increased CSF = expanded/dilated ventrilces = sretching of the _________ fibers = Normal P Hydrocephalus
Corona radiata fibers
76
Sx of NPH
Wet, wobbly, wacky
77
Lumbar puncture improves Sx
NPH (because removes some csf)
78
intracellular vacuoles
Spongiform encephalopathy
79
Dementia + ataxia + startle myoclonus (involuntary contractions with mild stimuli)
Spongiform encephalopathy
80
layer of gray matter in between internal capsule and ventricle
Caudate --> lost in Huntington = hydrocephalus ex vacuo
81
striatum
Caudate + Putamen (internal capsule in between them)
82
name a tumor that can cross the corpus callosum
GBM "butterfly lesion"
83
pseudopalisading and GFAP +
GBM (also, endothelial cell prolif)
84
benign tumor of ARACHNOID Villi/Cells
Meningioma
85
psamomma bodies + may present as seizure/focal neuro deficits
Meningioma
86
spindle cells in a concentrically whorled pattern
Meningioma
87
loss of hearing, tinnitis, s-100 +
schwannoma = benign tumor of schwann cells
88
neurofibromatous 2 brain tumor
bilateral schwannomas
89
calcified tumor in white matter, usually frontal lobe, seizures
Oligodendroglioma
90
where do you see a Pilocytic astrocytoma
posterior fossa/cerebellum
91
Cystic and solid components to neural tumor
Pilocytic astrocytoma: cystic lesion + mural nodule
92
Eosinophilic fibers of astrocytes on brain tumor biopsy
Rosenthal fibers --> Pilocytic Astrocytoma
93
Primitive neuroectodermal tumor (PNET): Name + Histo
Medulloblastoma: small blue cells
94
Homer-wright rosettes vs perivascular pseudorosettes
Homer-wright: Medulloblastoma, Neuroblastoma (AM) | Perivascular: Ependymoma
95
high mitotic index child brain tumor (posterior fossa)
Medulloblastoma = highly malignant
96
neuroblastoma
tumor of adrenal medulla in kids neural crest origin homer wright rosettes
97
brain tumor from epithelial origin
epithelial remnants of Rathke's pouch = Craniopharyngioma
98
Bitemporal hemianopsia in a child vs adult
child: consider Craniopharyngioma adults: Pituitary adenoma
99
how dos ectoderm become neuroectodorm = neural plate
Notochord (which becomes Nucleus polposus)
100
Neural plate gives rise to
Notochord and neural crest cells
101
Telencephalon and Diencephalon
Part of Forebrain (Football has TDs) Telencephalon: cerebral hem/lateral ventricles Diencephalon: thalamus/3rd ventricle
102
Midbrain/aqueduct come from which layer
Mesencephalon
103
AFP in spina bifida occulta
no structural herniation, just failure of bony spinal to close. intact dura. hair/skin simple. NORMAL AFP
104
maternal diabetes and messed up brain development
Anencephaly
105
Clinical findings of anencephaly
Polyhdramnios, increased AFP, no forebrain.
106
failure of L and R hemispheres to separate
Holoprosenchepaly
107
Conditions that cause Holoprosencephaly (failure R/L sep)
Patau, Fetal alcohol syndrome, Sonic hedgehog signaling pathway
108
Lumbosacral myelomeningocele
Arnold Chairi II (herniation through foramen magnum)
109
aquedecutal stenosis + hydrocephalus after cerebellar tonsillar herniation
Arnold Chiari II
110
cystic dilation of the 4th ventricle (posterior fossa)
Dandy walker
111
congenital hydrocephalus
structural: Aqueductal stenosis, Dandy walker, Chairi infectious: CMV, toxoplasmosis, meningitis
112
Sx of infantile hydrocephalus
``` Macrocephaly Poor feeding ("trouble latching while breast feeding") Muscle hypertonicity Hyperreflexia Seizures/developmental delay ```
113
why does infantile hydrocephalus cause hyperreflexia and hypertonicity (muscular)
UMN damage --> stretching of the periventricular pyramidal tracts
114
sensation/taste anterior 2/3 tongue 1/2 branchial arches
Sensation: V Taste: VII
115
sensation/taste posterior 1/3 tongue 3/4 branchial arches
IX (CN 9 = Glossopharyngeal)
116
role of Glossopharyngeal (CN9) and Hypoglossal (CN12) to tongue
9: taste and sensation of posterior 1/3 12 (Hypoglossal): Motor innervation to everything except for palatoglossus (X; elevates posterior tongue during swallowing)
117
Locus ceruleus (pons)
Norepinephrine Increased in anxiety Decreased in depression
118
Ventral tegmentum and Substantia nigra pars compacts (midbrain)
Dopamine
119
Basal nucleus of Meynert
ACh Increased in Parkinson Decreased in Alzheimers (AD = low ACh)
120
GABA (Nucleus Accumbens) levels in | anxiety and hungtingtons
Decreased in both
121
Stress and panic
Locus Ceruleus (NE)
122
Nucleus accumbens
GABA. Reward/pleasure/addiction/fear
123
Thalamic fibers going to primary somatosensory cortex
VPL (pain temp, MVP) VPM (face...sensation and taste) Damage to either = complete contralateral sensory loss dont be a peasant --> my impulse is "ventral" so has to be motor and not sensory
124
VPL nucleus of thalamus | vs in hypothalamus its like "ventromedial area"
Spinothalamic tract: Pain and temp DC/ML: MVP (proprioception, touch, vibration, pressure)
125
Patient has unsteady gait/difficulty walking. which track/nucleus of thalamus
VPL --> DC/ML = MVP = lost proprioception
126
VPM nucleus of thalamus
VPM --> Makeup goes on the Face Face sensation and taste
127
LGN and MGN of thalamus
LGN: "Light" = vision MGN: "Music" = hearing
128
VL nucleus of thalamus
Motor to Basal ganglia/cerebellum
129
The famous 5 F's = Limbic system
Feeding, Fleeing, Fighting, Feeling, Fucking | emotion, long term memory, behavior, ANS
130
structures of Limbic System
``` Hippocampus Amygdala Mammillary Body Fornix Cingulate Gyrus ```
131
Acute paralysis, dysarthria, dysphagia, diplopia, loss of consciousness
Osmotic demyelination syndrome aka central pontine myelinolysis
132
Cerebral edema/herniation related to Sodium
High to low, your brain will blow
133
Romberg
+: Ataxia is sensory = DC-ML fucked up | -: Ataxia is cerebellar
134
alpha synuclen intracellular eosinophilic inclusions
Lewy bodies --> Parkinsons and Lewy body dementia
135
resting tremor, shuffling gait
Parkinsons
136
Angry man with choreo (dancing movements), wheres the damage?
Caudate nucleus --> huntingtons
137
Neuronal death via NMDA-R binding and glutamate toxicity
Huntingstons: NMDA - Hunt with Glutamatate gun (NRA)
138
CAG Repeats and loss of ACh and GABA
Caudate loses ACh and GABA = Hungtingtons
139
No ifs, ands or buts (can't repeat)
Conduction Aphasia: damage to Arcuate Fasciculus. (poor repetition)
140
Disinhibited behavior: Hyperphagia, hypersexuality
Kluver-bucy --> amygdala lesion | Frontal lobe damage (R side = disinhibited behavior)
141
Reemergence of primitive reflex, difficulty concentration, poor judgement
Frontal lobe damage
142
Eye looks toward side of lesion
FEF
143
Eye looks away from lesion
PPRF
144
Stroke: Motor/Sensory to Upper Limb and Face
MCA
145
temporal lobe (wernicke) and frontal lobe (Broca) stroke
MCA
146
Lower limb motor and sensory loss
ACA
147
after stroke, can't walk
ACA (lower limb sensorimotor)
148
dysphagia, hoaseness, woming, decreased pain and temp from ipsilat face and cl body
PICA: lateral medulla (wallenberg)
149
Paralysis of face
AICA: Facial droop means AICAs pooped
150
intracranial hemorrhage that can cross suture lines
Subdural hematoma | i.e. shaken baby, alcoholics, blunt trauma/whiplash
151
intracranial hemorrhage that cross falx/tentorium
epidural hematoma
152
hemorrhagic stroke/intracerebral hemorrhage
Basal ganglia
153
lateral corticospinal tract (UMN)
voluntary movement of contralateral limbs
154
positive Romberg, absence of deep tendon reflexes, Latent bacteria
Tabes dorsalis
155
Tracts affected by vit b12 def
Subacute combined degeneration: DC-ML (lose mvp) Lateral corticospinal tract (UMN signs) Spinocerebellar tract Ataxic gait, parestheia, impaired position and vibration
156
KYPHOSCOLIOSIS, HCM, Staggering gait, frequent falling, PES CAVUS (high plantar arches)
``` Friedreich ataxia (trinucleotide repeat GAA) -->death by cardiomyopathy ```
157
Brown Sequard syndrome
hemisection of spinal cord CL pain and temp loss Ipsilateral loss of MVP, and UMN signs Ipsilateral loss of all sensation at level of lesion
158
UMN vs LMN face lesion
UMN: CL lower face paralysis LMN: ipsilat paralysis of upper and lower face
159
Neuroleptic Malignant Syndrome (after antipsychotic overdose)
diffuse muscle rigitidity high fever/ANS instability High Creatine kinase (rhabdomyolysis) Tx = Dantrolene (block Ca rel from RyR of SR) or Bromocriptine (dopamine agonist)
160
2 most common causes of intellectual disability
``` Down syndrome (most common overall) Fragile X (most common inherited) ```
161
CNIII is motor/sensory/both?
Pure MOTOR Some Say Marry Money But My Brother Says Big Boobs Matter Most
162
Radial Nerve Damage (include vs spare triceps reflex)
In Axilla (crutches/saturday night palsy) = Proximal injury = lose finger extensors, get wrist drop, absent triceps reflex Injury to proximal radial nerve as it crosses posterior humerus (MIDSHAFT HUMERUS) spares triceps reflex, lose extensors of hand. Finger/thumb drop (loss of extension) without wrist or tricep deficits = damage in supinator canal, i.e. mechanic doing lots of screwdriving
163
B12 deficiency rxns
MMA ---MMA CoA mutase --> Succinyl-CoA (not succinylcholine) Homocysteine --Methionine synthase/THF-->Methionine
164
rxn in PKU
lose PH or its cofactors tetrahydroBiopterin (BH4) | Phenylalanine--Phenylalanine Hydroxylase (PH) -->Tyrosine
165
Cerebellar lesions are different from cerebral because:
the cerebellum double crosses you! so ends up being ipsilateral. - ->dysdiadochokinesia (loss of rapidly alt movements) - ->limb dysmetria (over/undershoot) - ->intention tremor (tremor during movement)
166
2 CAN pneumonics
Whipples: Cardiac, Arthralgia, Neuro sx Wernicke: Confusion, Ataxia, Nystagmus (this is wernicke encephalopathy, not aphasia; and nystagmus interhcangable with opthalmoplegia. due to Thiamine b1 def) Note: Thiamine def = periph neuropathy, high-output cardiac failure, and Wernickes (ataxia, confusion, nystagmus)
167
Dx of Thiamine deficiency | periph neuropathy + cardiac failure aka wet beri beri DCM + Wernicke encephalopathy aka confusion ataxia nystagmus
Increased rbc TRANSKETOLASE activity after giving thiamine
168
Synaptophysin vs GFAP
GFAP = Astrocytes (NeuroGlia-->hence responsible for reactive GLIOSIS) -->Gliomas (non-neuronal tissue) = Astrocytoma, Ependymoma, Oligodendroglioma (still part of brain so still all neuroectoderm) Synaptophysin = neurons, neuroectodermal cells, neuroendocrine
169
Von Hippel Lindau (4)
1. Hemangioblastoma of cerebellum/retina (vascular) 2. Renal Cell Carcinoma (bilateral) 3. Pheochromocytomas 4. Angiomatosis (Cavernous hemangiomas all over)
170
difficulty removing hand from handshake
Myotonia (seen in myotonic dystrophy)
171
Frontal balding, cataracts, myotonia, testicular atrophy, arrythmia
Myotonic Dystrophy (type 1 fibers. auto dom trinuc rpt)
172
AICA vs PICA
Both: Ips P/T Face, CL P/T Body. Vomit/vertigo/nystag AICA: Lateral Pons. Facial paralysis. Taste ant 2/3 tongue (Facial droop means AICA pooped) PICA: Lateral Medulla. Dysphagia/hoarseness (dont pica horse that can't eat)
173
Locked-in syndrome
1. Osmotic Demyelination (central pontine myelinolysis) - ->correct hyponatremia (low to high pons will die) rapid 2. Basilar artery stroke Osmotic demyelination more likely to present with loss of consciousness
174
ACom or PCom: CNIII palsy
PCom. Both can cause visual defects. Both sites are more likely to be aneurysm than stroke. Both sites = Berry (saccular) aneyrums, with ACom #1
175
Motor and PNS component of CNIII
Motor in Middle: Affected by ischemia/ vascular dx (DM) -->Ptosis, Down-and-out gaze, Horizontal/vert diplopia PNS outside: Affected by compression (PCA aneurysm) -->dec Pupillary light reflex, Blown pupil with down/out
176
``` Vertical diplopia (can't go down the stairs) "With Cranial Nerve _____ its hard to walk down to the bottom floor" ```
``` CN IV (Trochlear = SO4) head tilts toward side of lesion, can compensatory tilt in other direction while going down stairs ```
177
Kid has MVP, autism, and intellectual disability. He has a problem in gene ________
Methylation ( Fragile X)
178
Kid has ASD, duodenal atresia, palmar crease, sandal gap. His b-HCG is ________, and his condition is a result of ______ _______
bHCG INCREASED in Down (dec in 18 and 13) Meiotic Nondisjunction
179
Elderly patient comes in with insomnia, can we give him Benzo?
NO!! Drugs to avoid in elderly: Benzo's: cognitive impairment/delirium/falls TCAs (amytriptyline) and antihistamines (Diphenhydramine) due to strong anticholinergic effects and delirium/falls
180
Temporal lobe herniation =
Uncal aka transtentorial herniation! Uncus = medial temporal lobe;
181
Uncal Herniation Manifestations
1. Ipsilateral CNIII = Ipsilat blown pupil/downandout 2. Ipsilateral PCA = contralat homonymous hemianopia 3. Compress CL Peduncle = CL Corticospinal tract = IPSILAT HEMIPARESIS 4. Duret hemorrhages: brainstem (pons/midbrain) due to stretching of Paramedian Basilar Artery (fatal)
182
Recurrent Lobar Hemorrhages in Elderly
Cerebral AMYLOID angiopathy
183
Endomysial inflammatory infiltrate Endoneural hyaline arteriolization Endoneural inflammatory infiltrate
Polymyositis (proximal mm weakness) Diabetic neuropathy GBS
184
Headache that gets worse with Valsalva (they will say its worse when he coughs or bears down during MM)
Suggests increased ICP aka tumor (and NOT a migraine)
185
contralateral Hemiparesis loss contralateral Hemisensory loss
Corticospinal tract lesion (cortical/brainstem) Ascending somatosensory = DC-ML and Anterolateral
186
Posterior Communicating Artery (PCom) Posterior Cerebral Artery (visual/occipital cortex) PICA (Lateral medulla)
PCom: saccular Aneurysm = COMPRESSES CNIII so see ipsilateral down and out + ptosis and myDRiasis PCA: Contralateral homonymous hemianopia w/macular sparing PICA: Dec P/T ipsilateral face and CL body; dysphagia, hoarseness, ipsilateral Horner; vomiting/vertigo/nystagmus
187
Parasympathetics vs Sympathetics eye
CNIII has PNS fibers on outside....so damage = MYDRIASIS (seen with compression= PCA aneurysm/Uncal herniation...won't really be seen with diabetic/vascular/ischemic damage unless severe) Horners = SNS damage = MIOSIS, ptosis, anhydrosis ------->any lesion above T1 i.e. Syringomyelia (c8-t1), Pancoast tumor, Brown-Sequard (hemisection resulting in CL P/T and Ipsi PICA: involves ipsilateral Horner (b/c knocks out SNS fibers)
188
Cerebellum Peduncles
Input: Inferior - ipsilateral info Middle - contralateral cortex info Output: Superior - Sends info to contral cortex to modulate movement (via output fibers = Purkinje fibers)
189
Lateral vs Medial Cerebellar Lesion (Romberg is - b/c cerebellar)
Lateral: Limb dysmetria (fall to ipsilat side) Medial: Truncal ataxia/nystagmus lose Rapid alt movements = dysdiadochokinesia also lose tandem walking in cerebellar lesion
190
Lesion location : Chorea (sudden, jerky movements. Huntington) Hemiballismus (sudden flailing of 1 arm, +/- Ipsi leg) Intention Tremor (zigzag when extending to target. MS)
Chorea: Basal Ganglia Hemiballismus: Contralat Subthalamic (Basal Ganglia -->Lacunar STROKE) Intention Tremor: Cerebellum
191
- Sudden uncontrolled muscle contraction(hiccups/jerks) - Sustained, involuntary muscle contraction (writer cramp) - High freq tremor w/sustained posture (outstretchedarm) - Tremor alleviated by intentional movement
Myoclonus Dystonia (also the eyelid thing. can manual suppress) Essential Tremor (relieve with EtOH) Resting tremor (parkinson)
192
Essential tremor tx
"Extremely tiring to keep my arm up" Have some EToH, bETa - blocker -pt self medicates with EtOH -Tx with Beta blocker or primidone
193
Dementia and visual hallucinations, followed by parkinsonian features
Lewy body dementia (Halewycinations) --> alpha-synuclein defect
194
Autoimmune myelin destruction (demyelinating)
``` Guillain Barre (PNS) Multiple Sclerosis (CNS). Can feel fatigue after hot shower ```