Chapter 28: Nervous System Part 2 Flashcards

1
Q

stroke: clinical symptoms and diagnosis
-signs and symptoms: Facial ______, ______,
inability/difficulty ______, weakness on ______,
______ on one side, numbness, disturbance in fine movements, ______ (unable to control urination). ______ patients mimic stroke symptoms
DIAGNOSIS:
-It is possible to distinguish a cerebral infarct from a cerebral hemorrhage by a ______
-______ provides similar information and is equally effective
-Manifestations of all these conditions related to strokes, depend on ______ and ______

A
Drooping
headache
speaking
one side
paralysis
Incontinence
Hypoglycemic
computed tomography CT scan
Magnetic resonance imaging (MRI)
location
size
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2
Q
Stroke- theres a treatment if you act FAST
F-
A-
S-
T-
A

face- look uneven
arm- one arm hanging down
speech- slurred speech
time- call 911 now

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3
Q

stroke treatment:

  • ______: Considered the gold standard, ______ (or Alteplase IV r-tPA) is the only FDA-approved treatment for ischemic strokes. TPA needs to be used within ______ hours of having a stroke or up to ______ hours in certain eligible patients. The goal is less damage to ______ (area of the brain which receives low oxygen due to the stroke).
  • Physical removal (within 6 to 7 hours of onset only after a patient receives ______) of a large blood clot, called an ______ or a ______, is another strongly recommended treatment option.
  • ______: A small tube called a catheter can sometimes be threaded up through a ______ in an ______ or ______ and guided into the brain tissue, allowing the surgeon to use camera technology to help fix the problem.
  • Once the catheter is guided to the source of the bleeding, it deposits a ______, such as a coil, to prevent further rupture.
  • This type of procedure is ______, meaning that the surgeon gains access via the vascular system, making it less invasive than conventional surgical treatment.
  • Sometimes ______ is required to secure a blood vessel at the base of the ______.
A
Ischemic Stroke
tissue plasminogen activator
three
4.5
penumbra
TPA
endovascular procedure
mechanical thrombectomy
Hemorrhagic stroke
major artery
arm
leg
mechanical agent
endovascular
surgery
aneurysm
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4
Q

-Inflammation of the leptomeninges. Meninges consist of three layers (______, ______, and ______) that lie between the ______ and the ______
-______ and ______ together are known as leptomeninges.
-Pyogenic meningitis: ______, ______, and ______ (neonates) ______ (children and teenagers), ______ (adults and elderly), and ______ (non-vaccinated infants).
-Viral meningitis: ______ virus, ______ (children; fecal-oral transmission), ______ & fungal (immunocompromised individuals)
SYMPTOMS, PATHOGENESIS, and TREATMENT
-Presents with classic triad of ______, ______ (neck stiffness) & ______; ______, vomiting, and altered mental status (sometimes). Complications are usually seen with ______. Death: _____ meningitis secondary to ______. Hydrocephalus, hearing loss, and seizures
-Spinal tap (between __ & __): sampling of CSF
-______: Purulent exudate w/in leptomeninges, dilated ______. Lab findings: ____ CSF with ______, ↑ ______ & ↓ ______. ______ for identifying the bacteria.
-______: lymphocytes with normal CSF glucose.
-______: lymphocytes with ↓ CSF glucose
-Treatment: Pyogenic (______ & ______ as needed), Viral (self limiting & ______) & fungal (______ & ______)

A
meningitis 
dura, arachnoid, and pia
brain
skull
Pia
arachnoid
Group B streptococci
Ecoli
Listeria monocytogenes
Neisseria meningitis
Streptococcus pneumoniae
H influenza
HSV
Coxsackievirus
echovirus
headache
nuchal rigidity 
fever
photophobia
bacterial 
herniation
cerebral edema
L4
L5
Pyogenic
meningeal vessels
neutrophils 
protein
CSF glucose
Gram stain
Viral
Fungal
antibiotic
steroid 
anti-viral
anti-fungal
steroid
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5
Q
  • Follows viral (EBV,HSV&CMV) infection (demyelination of ______ via ______ mediated immune reaction)
  • ______ and ______ in legs & ______ muscle weakness. Rapidly progressive ______
  • May cause ______
  • Reversible disease & Spinal injury may affect ______ or ______ properties.
  • Diagnosis; ______: CSF with large ______ count with mild ______ count increased.
  • treatment: supportive/resuscitative interventions & IV ______
A
Guillain-Barre Syndrome
demyelination
neurons
T-cell
Weakness
tingling 
ascending 
paralysis
respiratory failure/arrest
CNS
cognitive
Lumber puncture/spinal tap
protein
cell
IgG
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6
Q
  • Caused by small protein particle produced and resistant to ______. Only inactivated by ______ for __ hour.
  • The normal form of protein is the “good prion” designated ______. The abnormal form of protein is the “bad prion” designated ______. Transmission is thought to be by exposure to (most commonly by ingestion of) ______ (or human) tissue, particularly, but not exclusively, brain.
  • These disorders are anatomically defined by the finding of ______ (spongiosis), which is characterized by clusters of ______ in CNS ______ matter, along with a striking absence of inflammatory response.
A
Creutzfeldt-Jakob/mad cow Disease
heat/sterilization
1M NaOH
1
PrPc
PrPsc
prion-containing animal
spongiform encephalopathy
small cysts
gray
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7
Q

Multiple sclerosis: (Autoimmune disease)
PATHOGENESIS:
-______ within the ______ of CNS (scattered in the brain and spinal cord). Gross examination shows ______ in the ______ matter. Helper ______ and cytotoxic ______ T lymphocytes and macrophages infiltrate plaques.
-women affected ______ as often as men
-associated with HLA-______
-characteristics also include depletion of ______-producing ______.
-Presents with relapsing ______ with periods of remission (multiple ______ in time and space).
-remission of neurologic symptoms: Charcot’s triad: ______, ______, & ______
-sensory abnormalities: Loss of sensitization of ______
-motor abnormalities: ______ weakness, ______, ______, and ______ dysfunction (______ nervous system)
-

A
Demyelinatinon
white matter
gray-appearing plaques
white
CD4+
CD8+
twice
DR2
myelin
oligodendrocytes
neurologic deficits
lesions
nystagmus, scanning speech & tremor 
touch
Muscle
bowel
bladder
sexual
autonomic
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8
Q

multiple sclerosis diagnosis and treatment
-Diagnosis: ______ and ______.
MRI reveals plaques (areas of _____ matter demyelination) Lumbar puncture shows increased ______, increased immunoglobulins with ______ bands on high resolution electrophoresis, and myelin basic protein.
-______: The most common treatment for multiple sclerosis, corticosteroids reduce the inflammation that spikes during a relapse. Examples include ______ and ______.
-______ (such as Betaseron, Avonex and Rebif) appear to slow the rate at which multiple sclerosis symptoms worsen over time. Side effects are ______ damage.

A
MRI 
lumbar puncture
white
lymphocytes
oligoclonal IgG
Corticosteroids
oral prednisone
intravenous methylprednisolone
Interferons
liver
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9
Q

The mechanism by which dimethyl fumarate (DMF) exerts its therapeutic effect in multiple sclerosis is unknown. DMF and the metabolite, ______, have been shown to activate the Nuclear factor ______ pathway in vitro and in vivo in animals and humans. The Nrf2 pathway is involved in the cellular response to ______. MMF has been identified as a ______ in vitro.

A
TECFIDERA
monomethyl fumarate (MMF)
(erythroid-derived 2)-like 2 (Nrf2)
oxidative stress
nicotinic acid receptor agonist
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10
Q

Metabolic disorder of the Nervous System

  • inborn errors of metabolism:
  • ______: Can’t degrade the amino acid phenylalanine
  • ______: Deficiency of HGPRT enzyme (hypoxanthine-guanine phosphoribosyl transferase): self mutilation & involuntary movements.
A

Phenylketonuria

Lesch-Nyhan Syndrome

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11
Q

chronic alcoholism

  • ______: Characteristics include loss of memory & ______ associated with chronic alcoholism and deficiency of ______(vitamin B1). Reversible.
  • ______: Characterized by disorientation, ______, delusion. Patient often complain of painful ______ with ______ pains. May be irreversible.
  • ______: Characterized by rapid onset of disorganized thought process.
A
wernicke's syndrome 
disorientation
thiamine 
korsakoff syndrome
insomnia
extremities
nerve
Delirium
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12
Q

Neurodegenerative Diseases

  • ______ disease
  • ______ disease
  • ______ disease
  • ______ (Lou Gehrig’s disease): ALS
A

alzheimers
parkinsons
huntingtons
amyotrophic lateral sclerosis

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13
Q

Most important cause of dementia. This disease was formerly viewed as ______ occurring in middle-aged persons (pre-senile dementia); the entity now includes dementia at any age if it is associated with characteristic clinical and pathologic findings.
-______ of the cortical parts of the ______ and ______ parts of the brain
-Disease of older people (>70 years). Patients become ______ and ______; ______ is a common cause of death.
-______—progressive loss of cognitive functions
and a functional decline (loss of memory
predominates)
PATHOGENESIS
-The brain appears atrophic and shows narrowing of
the ______ and a widening of the ______
-Neuritic (senile) plaques: cluster with ______). Aβ amyloid is derived from ______, which is coded on chromosome ___. APP normally undergoes ______ (breaks) and ______ results in Aβ amyloid. Amyloid may also deposit around vessels, increasing the risk of ______.
-Neurofibrillary tangles: ______ (Defective)
-Genetic risk: E4 allele of apolipoprotein E (APOE) is associated with ______ risk, E2 allele with ______ risk.
-______: AD occurs by 40 years of age
-Diagnosis: ______ scan for early diagnosis.
-Treatment: ______ to slow progression. Progressive disease with no cure.

A
alzheimers disease
premature senility
atrophy
frontal
temporal
mute
bedridden
infection
Dementia
gyri
sulci
Aβ amyloid
amyloid precursor protein (APP)
21
alpha cleavage
beta cleavage 
hemorrhage
TAU proteins 
increased
decreased
Down syndrome
PET/MRI
Acetylcholinesterase inhibitors
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14
Q
  • Cause dementia, affects more women. It is characterized by cortical _____ and accumulation of ______ (cytoplasmic inclusion bodies made of ______).
  • Treatment: Treat the ______ and ______ symptoms arise early.
  • ______ disease with no cure
A
pick disease
atrophy
Pick bodies
neuro filaments
Behavioral
language
progressive
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15
Q

parkinson disease

  • subcortical neurodegenerative disorder
  • Decreased number of ______ in the substantia nigra of the ______.
  • Histologic manifestations include ________ of the substantia ganglia and damaged cells contain highly characteristic eosinophiliic intracytoplasmic inclusions ( _____bodies).
  • Idiopathic Parkinson disease damages neuronal pathways from the ______ to the ______, resulting in ______.
  • Clinical features (______): Tremor-pill rolling tremor at rest & disappears with ______
  • Rigidity: ______ rigidity in the extremities
  • ______: slowing of voluntary movement & expressionless face
  • Postural instability
  • Treatment: ______, ______ and Deep brain stimulation.
  • Causes: Idiopathic, ______, ______ such as MPTP (methyl-phenyl-tetrahydropyridine), a contaminant in illicit street drugs.
  • ______, parkinsonism with autonomic dysfunction and orthostatic hypotension.
A
dopaminergic neurons
basa ganglia
depigmentation
Lewy bodies
substantia nigra
corpus striatum
dopamine depletion 
'TRAP'
movement
cogwheel
Akinesia/bradykinesia
L-DOPA
Dopamine agonist
trauma
dopamine antagonists 
Shy-Drager syndrome
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16
Q
  • Autosomal dominant neurodegenerative disease: chromosome # ___ (______ repeat)– 6 to 35
  • ______, ______ movements and progressive ______ and depression (average age 40).
  • atrophy of the ______ and ______, most prominently the ______ and ______ and degeneration of GABA generating neurons in these areas.
  • ______ is a common cause of death.
A
huntington's disease
4
CAG
Involuntary
gyrating
dementia
cortex 
subcortical nuclei 
caudate
putamen
Suicide
17
Q
  • Neurodegenerative disease and affects older men and women over 40 +. It is the most common form of ______ disease
  • Characteristics include degeneration and atrophy of the ______ tracts, as well as of the ______ neurons of the cord.
  • ______ weakness and progressive ______ in the extremities (small hand muscles). involuntary ______. slurred speech but the _____ is not affected
  • clinical onset occurs in early middle age, with a ______ course leading to death (most often from ______) in 1 to 6 years.
A
Amyotrophic Lateral Sclerosis (ALS, Lou Gehrig disease)
motor neuron 
lateral cortico spinal
anterior motor 
motor
wasting of muscles
twitching
intellect
rapid
respiratory failure
18
Q

neoplasms of the CNS

  • brain tumors have a ______ mortality rate
  • brain tumors occur at ______ age
  • of tumors, ___ are primary neoplasms
  • they may be ______ or ______
  • malignant tumors of the CNS do not ______
A
very high
any
50%
benign
malignant 
metastasize
19
Q
  • are the most common primary brain tumors. They can be divided based on their infiltration into the surrounding brain ______. Composed of relatively ______
  • Astrocytomas that do not infiltrate the brain include ______ astrocytomas, ______ ______, and subependymal ____ cell astrocytomas.
  • diffuse astrocytomas can be further subdivided based on ______
  • Low-grade fibrillary astrocytomas are WHO grade ___.
  • anaplastic astrocytomas are WHO grade ___
A
astrocytomas
parenchyma
well-differentiated astrocytes
pilocytic
pleomorphic
xanthroastrocytomas
giant
grade
II
III
20
Q
  • Malignant, high-grade tumor of astrocytes
  • Most common primary malignant CNS tumor in adults
  • Usually arises in the ______; characteristically crosses the corpus callous (______)
  • this neoplasm is associated with marked ______ and ______; pronounced vascular changes with endothelial hyperplasia occur. Areas of necrosis and hemorrhage are surrounded by a ______ arrangement of tumor cells.
  • ______ prognosis: death within year of diagnosis.
A
glioblastoma multiforme 
cerebral hemisphere
butterfly' lesion
anaplasia
pleomorphism 
“pseudopalisade”
Poor
21
Q
  • This neoplasm presents as a slow-growing tumor in the middle-age group and typically arises in the ______. It originates in oligodendrocytes.
  • Imaging reveals a ______ tumor in the ______ matter, usually involving the ______ lobe. It may present with ______
  • ______ appearance of cells on biopsy.
  • A ______ between chromosomes ___ and ___ is the characteristic molecular signature.
A
oligodendrogliomas 
cerebral hemispheres
calcified
white
frontal
seizures
'Fried-egg'
translocation
1p
19q
22
Q
  • This neoplasm most frequently occurs in the fourth ventricle. Peak incidence is in childhood and adolescence.
  • Histologic characteristics include ______ or ______ with cells encircling vessels or pointing toward a central lumen and tumor cells characteristically demonstrate ______ structures near the nucleus representing ______ of cilia.
  • Results may include papillary growths that obstruct flow of CSF and lead to ______.
A
ependymomas
tubules
rosettes
rod-shaped
basal bodies
hydrocephalus
23
Q
  • arise from the meninges. mostly benign. it is the second most common primary intracranial neoplasm (WHO-__ grade)
  • Most common benign CNS tumor in adults
  • More commonly seen in ______; rare in ______
  • may present as ______ when tumor compresses, but does not invade the ______. presence of ______ (laminated calcifications)
  • imaging reveals a round mass attached to the ______
A
meningioma 
1
women
children
seizures
cortex
psammoma bodies
dura
24
Q

tumors of the cranial and spinal nerves
-______ (neurilemmoma): benign, slowly growing ______ tumor arises from ______ cells.
-When intracranial, it is most frequently localized to the ______ cranial nerve (acoustic neuroma, acoustic schwannoma); third most common primary intracranial neoplasm. It also originates in ______ nerve roots and ______ nerves.
-It has two patterns:
______: interlacing bundles of elongated cells with palisading nuclei
______: looser, less cellular pattern than Antoni A

A
Schwannoma
encapsulated
Schwann
eighth
posterior
peripheral 
Antoni A
Antoni B