CSF and hydrocephalus Flashcards

1
Q

what makes CSF? where is most CSF made?

A
  • choriod plexus ependymal cells (choroidal epithelium) inside of the ventricles
  • mainly in the lateral ventricle
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2
Q

where are the tight junctions of the BBB and the Blood-CSF barrier

A

BBB- continous with endothelial lining (facing the blood side) [ non fenestrated capillary lining]

BCB - continous with choroid cells (on the CSF side)
[fenestrated capillary endothelial lining]

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3
Q

what is the function of the astrocyte foot cells in the BBB

A

needed for BBB development
(type of glial cell)

-regulate water intake inside the brain

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4
Q

what is more permeable, BBB? blood-csf barrier ?

A

blood csf barrier

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5
Q

Blood CSF barrier impairment leads to an increase in ___ concentration of the CSF

A

protein

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6
Q

what are the steps of CSF production?

A
  1. filtration- filtered blood passes capillary fenestrations and enters choroidal cells in the ventricles due to pressure gradient between the CSF and blood
  2. active transport of fluid into the ventricles
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7
Q

how to test for composition and pressure of CSF

A

lumbar puncture between L3/L4 or L4/L5

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8
Q

blood and CSf differ ___ not _____

A

differ quantitatively not qualitatively

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9
Q

t/f

you have 2 lateral ventricles

A

true

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10
Q

how does CSF leave the 4th ventricle

A
  1. continuous with central canal down into spinal cord
  2. foramen of luschka- 2 lateral apertures moves CSF back to subarachnoid space in brain then to superior sagitall sinus to drain in venous circulation via subarachnoid villi
  3. foramen of magendie - 1 medial aperture moves CSF back to subarachnoid space brain then to superior sagitall sinus to drain in venous circulation
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11
Q

what happens if CSF pressure > venous pressure ? venous pressure > CSF pressure?

A

CSF pressure > - flow of CSF into venous sinuses

Venous pressure> - no flow of CSF **no retrograde flow possible

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12
Q

how is CSF replenished once the CSF has left the brain via the venous sagitall sinuses

A

goes to heart, gets filtered back to arterial blood, enters the brain again and replenishes CSF via choroid plexuses in each ventricle

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13
Q

disorder of excessive CSF accumulation in the cerebral ventricles or subarachnoid space that causes ventricular dilation and increased inter cranial pressure

A

hydrocephalus

*expansion of ventricular system

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14
Q

causes of hydrocephalus

A
  1. CSF overproduction
  2. CSF under -reabsorption at level of arachnoid villi
  3. obstruction
1-2 = communicating (flow of CSF blocked after leaving ventricles, or too much made) 
3 = non-communicating
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15
Q

t/f

communicating hydrocephalus is typically associated with increased ICP

A

true

*except hydrocephalus ex-vacuo

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16
Q

what are the triad of symptoms associated with normal pressure hydrocephalus {NPH) ? what type of hydrocephalus is it? possible causes ?

A

*chronic communicating hydrocephalus - [underabsorption]

dementia
apraxic gait
urinary incontinence

casuses: increased CSF viscosity, change of ventricle elasticity, impaired absorption

  • apraxic gait = frontal lobe disorder in which patient can not initiate walking but has the motor function to walk still intact
  • common in the elderly
17
Q

how is the CSF pressure affected in Normal pressure communicating hydrocephalus ?

A

intermittently elevated

18
Q

what type of hydrocephalus is hydrocephalus ex-vacuo? possible causes? common symptoms ? associated ICP?

A
  • communicating [ overproduction ]
  • brain atrophy, post traumatic brain injury, psychiatric disorders
  • no increased ICP (bc increases CSF production tries to keep weight of brain constant with loss of brain tissue)
  • symptoms : blurred vision, headaches, n/v, drowsiness
19
Q

what is aqueductal stenosis ? common signs/symptoms ? common causes ?

A
  • narrowing of the cerebral aqueduct between 3rd and 4th ventricle leading to obstruction of CSF flow and non-communicating hydrocephalus
  • sx: thunderclap headaches, papilledema, cognitive delays, difficulty looking up, tremors, (infant) enlarged head

-causes: tumor compression, narrow duct, gliosis (hypertrophy of glial cells due to CNS damage)

20
Q

what is dandy-walker malformation ?

A

-congenital brain malformation in which agenesis/hypoplasia of the cerebellar vermis causes the 4th ventricle to be open to the posterior fossa, this leads to CSF accumulation in the posterior fossa and a “dandy walker cyst” which enlarges after birth and causes compression of the central canal which leads to 4th ventricle obstruction
[cerebellar hyoplasia + CSF cyst + 4th ventricle obstruction]
-noncommunicating hydrocephalus
-symptpms slow motor development, enlarged skull (present at birth)

21
Q

what is arnold Chiari type 2 malformation ?

A
  • displacement of the cerebellar tonsils, medulla, and 4th ventricle down passed the foramen magnum into cervical canal possibly (90%) causing aquaductal stenosis and non-communicating hydrocephalus
  • associated with myelomeningocele
  • causes: embryo malformation
  • *presents at birth