CSF Flashcards

1
Q

a major fluid of the body

A

Cerebrospinal fluid (CSF)

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2
Q

Functions of CSF

A
  • supply nutrients to the nervous tissue
  • remove metabolic wastes
  • produce a mechanical barrier to cushion the brain and spinal cord against a trauma
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3
Q

brain and spinal cord are lined by

A

Meninges

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4
Q

meninges consist of 3 layers

A

Dura mater, arachnoid, pia mater

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5
Q
  • Latin for hard mother
  • outer layer that lines the skull and vertebral canal
A

Dura mater

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6
Q

spiderweb like, filamentous inner membrane

A

Arachnoid

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7
Q

gentle mother, thin membrane lining the surfaces of the brain and spinal cord

A

pia mater

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8
Q

CSF is produced in the _ of the lateral, third, and fourth ventricles

A

Choroid plexuses

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9
Q

Fluid produced every hour for adults

A

20 mL of fluid

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10
Q

the fluid flows through the - located between the arachnoid and pia mater

A

Subarachnoid space

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11
Q

volume of CSF maintained in adults

A

90 to 150 ML

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12
Q

volume of CSF maintained in neonates

A

10 to 60 ml

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13
Q

to maintain a specific volume in adults and neonates, the circulating fluid is reabsorbed back into the capillaries in the

A

Arachnoid granulations / villae

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14
Q

Are capillary networks that form the CSF from plasma by mechanisms of selective filtration

A

Choroid plexuses

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15
Q

capillary walls throughout the body are lined
with

A

endothelial cells

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16
Q

loosely connected to allow passage of soluble nutrients and wastes between the plasma and tissue

A

Endothelial cells of capillary walls

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17
Q

Have very tight fitting junctures that prevent the passage of many molecules

A

endothelial cells of choroid plexus

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18
Q

tight fitting structure of the endothelial cells in the choroid plexuses

A

blood brain barrier

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19
Q

CSF is routinely collected by

A

lumbar puncture

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20
Q

location of CSF collection

A

between the 3rd, 4th, or 5th lumbar vertebra

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21
Q

CSF specimens are collected in

A

three sterile tubes

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22
Q

Tube I

A

chemical and serologic test, least affected by blood or bacteria

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23
Q

Tube 2

A

usually designated for the microbiology laboratory

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24
Q

Tube 3

A

is used for HEMA/ cell count, its the least
likely to contain cells introduced by the spinal
tap procedure

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25
how hematology tubes are maintained
refrigerated
26
microbiology tubes are maintained by
remain at room temp
27
chemistry and serology are maintained by
frozen
28
initial appearance of normal CSF
crystal clear
29
3 types of epithelial cells
ependymal calls, choroidal cells, PAM cells
30
used to describe CSF supernatant that is pink, orange, or yellow
Xanthochromia
31
most common cause of xanthochromia
RBC degradation products
32
grossly bloody CSF can be an indication of
Intracranial hemorrhage
33
Cause and indication of a hazy, turbid,milky, cloudy CSF
Meningitis
34
Microorganisms in CSF is an indication of
Meningitis
35
Protein in CSF is an indication of
- Disorders affecting blood-brain barrier - production of IgG within the CNS
36
Oily appearance of CSF may be the cause of
Radiographic contrast media
37
Cause and indication of bloody CSF
- RBC - hemorrhage or traumatic cap
38
Xanthochromic CSF because of hemoglobin is an indication of
Old hemorrhage, lysed cell from traumatic cap
39
Xanthocromic CSF because of bilirubin may be an indication of
RBC degradation, elevated serum bilirubin level
40
Xanthocromic CSF because of carotene may be an indication of
Increased serum levels
41
Xanthocromic CSF because of protein may be an indication of
Disorders affecting blood-brain barrier
42
Xanthocromic CSF because of melanin may be an indication of
Meningeal melanosarcoma
43
Clotted CSF because of clothing factors
Introduced by traumatic tap
44
Pellicle appearance in CSF because of dotting factors is an indication of
Tubercular meningitis
45
WBCs ( particularly granulocytes) and RBCs begin to lyse within
1 hour
46
40% of the leukocytes disintegrate after
2 hours
47
Dilution ratio for CSF
1:20 or 1:10 (if clear no need to dilute)
48
CSF cell count formula
Ave no. of cells counted x dilution/ no. of squares counted x volume of 1 square
49
Preferred centrifuge for CSF specimen
Cytocentrifuge
50
When one differential count is performed _should be counted, classified, and reported in terms of percentage
100 cells
51
High CSF WBC count of which the majority of the cells are neutrophils are indicative of
Bacterial meningitis
52
Major clinical significance of lymphocytes
- Normal - viral, tubercular, fungal meningitis - multiple sclerosis
53
Microscopic findings of lymphocytes
All stages of development may be found
54
Major clinical significance of neutrophils
- Bacterial meningitis - early cases of vital,tubercular, and fungal meningitis - cerebral hemorrhage
55
Microscopic findings of neutrophils
- Granules maybe less prominent than in blood - cells disintegrate rapidly
56
Monocytes major clinical significance
- Normal - viral, tubercular, fungal meningitis - multiple sclerosis
57
Microscopic findings of monocytes
Found mixed with lymphocytes
58
Major clinical significance of macrophages
RBCs in spinal fluid
59
Microscopic findings of macrophages
May contain phagocytized RBCs appearing as - empty vacuoles or ghost cells, - hemosiderin granules, and - hematoidin crystals
60
Blast forms major clinical significance
Acute Leukemia
61
Blast forms microscopic findings
Lymphoblasts, myeloblasts, or monoblasts
62
Major clinical significance of lymphoma calls
Disseminated lymphoma
63
Microscopic findings of lymphoma cells
Resemble lymphocytes with cleft nuclei
64
Major clinical significance plasma cells
Multiple sclerosis, lymphocyte reactions
65
Plasma cells microscopic findings
- Traditional and classic forms seen - reactive lymphs
66
Major Clinical Significance Of Ependymal, choroidal, and spindle-shaped cells Malignant cells
Diagnostic procedures
67
Microscopic findings of Ependymal, choroidal, and spindle-shaped cells
Seen in clusters with distinct nuclei and distinct cell walls
68
Major clinical significance of malignant cells
Metastatic carcinomas, primary CNS carcinoma
69
Malignant cells microscopic findings
Seen in clusters with fusing of cell border and nuclei