CNS pathology- 2 Flashcards

1
Q

What are astrocytomas?

A

glial neoplasms derived from astrocytes

75-80% of adult primary brain tumors

usually middle age or older

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Where are Astrocytomas usually found?

A

Adults- in the cerebral hemispheres

Peds- Cerebellum and the pons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Grade I Astrocytoma

A

20% of primary intracranial neoplasms

  • poorly demarcated
  • infiltrates the cortex
  • indistinct margin
  • can also be seen in the pons/cerebellum in peds and cervical spinal cord in young adults
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the life expectancy for a Grade I Astrocytoma?

A

~5 years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How do you distinguish Anaplastic (Grade II) Astrocytoma from a well-differentiated astrocytoma?

A
  • Greater cellularity
  • Cellular pleomorphism
  • Anaplasia

*distribution parallels that of Grade I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the growth and life expectancy of an Anaplastic (Grade II) Astrocytoma?

A

growth is rapid

life expectancy= ~3yrs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Glioblastoma Multiforme (GBM)–> AKA grade III astrocytoma

A
  • 40% of primary intracranial neoplasms
  • life expectancy= 18mo
  • Infiltrates extensively into cortex, often crossing the corpus callosum w/ bilateral extension into the white matter of both hemispheres
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is seen on gross examination of Glioblastoma Multiforme (GBM)?

A

-Both bottled red (recent hemorrhage) and yellow (remote hemorrhage) likened to a butterfly on gross examination

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What differentiated oligodendrogliomas from other tumors?

A
  • well-circumscribed, gelatinous, grey masses, often with cysts, focal hemorrhage and calcification
  • Slow growth is reflected by absence of mitotic figures and necrosis (so better prognosis than astrocytomas)
  • common complaint: seizures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the most common presentation of Epenymomas?

A

-hydrocephalus secondary to progressive obstruction of the 4th ventricle (whee they are commonly located) x

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What chromosomal aberration is seen in meningiomas?

A

Majority arise sporadically and exhibit either a deletion or mutation of chromosome 22

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the characteristic cell that is seen in Parkinsons disease?

A

Lewy Bodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the number 1 etiology as to why Hypertensive bleeds occur that are related to HTN?

A
  • Charcot-Bouchard aneurysms (formed from the weakening of the walls of cerebral arterioles) are predisposed to rupture and cause hypertensive cerebral rupture
  • Have a graphic distribution
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the number one etiology of why strokes occur?

A

Artherosclerosis- predisposes to vascular thrombosis and embolic events –> both result in ischemia and subsequent cerebral infarction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is are meningiomas?

A
  • intracranial tumors that arise from the arachnoid villi and produce sxs by compressing brain tissue.
  • 20% of intracranial tumors
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is the peak incidence of meningiomas?

A

4th-5th decades

Slightly more common in females (60:40)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Where are meningiomas most commonly located?

A

In the parasagittal areas, convexities of the cerebral hemispheres, the olfactory groove and the lateral wing of the sphenoid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What do meningiomas have a propensity to do?

A

erode contiguous bone

20
Q

Other than chromosomal abberations, what else can cause meningiomas?

A

Cranial radiation (related to dosage)

21
Q

How do meningiomas appear grossly

A

well-circumscribed, firm, bosselated masses of variable size

-cut sections show a gray, fibrous patter

22
Q

What is the clincial presentation of meningiomas?

A

depending on location, seizures rather than neuro deficits characterize the pt (due to lesions positioned in the parasagittal and over the convexities of the hemispheres)

23
Q

Clinical presentation of meningiomas

A

tumors in the olfactory groove produce ansomnia

Tumors in suprasellar region- visual defects

HA’s common

24
Q

What is Kernig sign?

A

Pain in the knee when the hip is flexed

–> sign of bacterial meningitis

25
What is the Brudzinski Sign?
Spontaneous flexion of the knees and hips when the neck is flexed --\> sign of bacterial meningitis
26
What are two special physical exam tests you can perform on a patient to test for bacterial meningitis?
Kernig and Brudzinski signs += bacterial meningitis
27
What is an Acoustic Neuroma?
- Intracranial Schwannoma that is restricted to CN8 - Malignancy is rare
28
Symptoms of Acoustic Neuroma
1. tinnitus 2. Deafness Can also compress other Cranial nerves
29
Where are Acoustic Neuromas usually found?
- Found in the cerebellar pontine angle - restricted to CN8
30
What is Multiple Sclerosis?
A chronic, demyelinating dz of the CNS which there are numerous patches of demyelination throughout the white matter - Affects both sensory and motor functions - Characterized by exacerbations and remissions over several yrs
31
What is the prevalence of MS?
Most common demyelinating disorder 1 in 1000
32
What is the etiology of MS?
unknown experimental studies point to possible genetic, immune and infectious etiology
33
What are early symptoms of MS? What is often the presenting complaint?
- blurred vison or unilateral vision loss - double vision - vertigo
34
Who is most likely to get MS?
- Usually occurs in temperate climates (rare in tropics) - Acquired at mean age of 30. Rare \<14y/o and \>60 - Women afflicted 2x more than men
35
Genetic factors associated with MS
suggest a familial aggregation of the dz w/ an increased risk in 2nd and 3rd degree relatives
36
What are immune factors related to MS?
Immune factors are related to the histologic appearance of lesions: perivascular lymphocytes and macrophages with numerous CD4+ and CD8+ T-cells
37
What viruses are associated with MS?
measles mumps rubella herpes \*no direct evidence exists for this involvement
38
What is the hallmark of MS?
the plaque -variable in sz w/ smooth rounded contour
39
Where is the plaque, that is a hallmark of MS, located?
Usually situated in the white matter occasionally breech the gray-white junction - shows a preference for optic nerves and chiasm and uniformly localizes to the periventricular white matter - Can also involv the cerebellum brainstem and SC (but mainly around the ventricles)
40
What happens as the plaque in MS ages?
- it becomes more discrete and the edema regresses - Astrocytes traverse the aging plaque and the tissue becomes dense with glial processes
41
What symptoms are seen in a patient with MS if the plaques are within the spinal cord?
- weakness of one or both legs - numbness in the lower extremities
42
Are the initial sxs of MS reversible?
many of the initial sxs are partially reversible w/in a few months
43
What is the degree of functional impairment in MS?
variable. Ranges from minor disability--\> sever incapacity with widespread paralysis, dysarthria, severe visual defects, incontinence and dimentia
44
How do patients with MS usually die?
usually die of respiratory paralysis or UTIs in terminal coma
45
What is the prognosis of MS?
Most patients survive 20-30 years after onset of sxs