Pathology Flashcards

1
Q

red neurons are:

A

shrinkage of cell bodies and pyknosis of nucleus
esinophilia

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2
Q

spheroids are
central chromatolysis

A

peripheral displacement and nissl bodies and body enlargemnt

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3
Q

inclusions are seen in:
acccumulation of liofuscin seen in and what is the stain
tay sachs dis is:

A

viral dizs
older ppl \ wear and tear
ganglioside lipid accumilation

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4
Q

gemistocytes are ____ and seen in ____

A

swollen astrocytes that are acidophilic cytoplasim
tumor

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5
Q

rosenthal fibers are seen

A

old gliosis

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6
Q

macrophages in infarction

A

gitter cells

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7
Q

macrophages in syphilis

A

rod cells (elongated)

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8
Q

microglial cells around injured cells

A

microglial nodules

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9
Q

microglial cells around dead neurons is

A

neuropahgia

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10
Q

most common route of infection for CNS

A

hematogenous

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11
Q

selective sites for all of
CMV
HSV
polio
VZV

A

ependymal cells
temporal and orbital
anterior horn of spinal cord
thoracic dorsal root inclusions

cytoplasmic inclusions in rabies
nucleus inclusions in CMV

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12
Q

vulnirability of CNS tissue to hypoxia

A

pyramidal cells in hippocampus
purkinji cells in cerebellum
basal ganglia
watershed areas

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13
Q

watershed areas include:

A

area between MCA and ACA
between PCA and MCA
between superior cerebellar and posterior cerebellar

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14
Q

very hemorrhageic cuz of thin wall

A

venous sinus thrombosis (venous infarction)

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15
Q

datings of infarcts:
red neurons
neutrophils
macrophages
astrocytes and peak at
macrophages leaving

A

12-24
1-3days
1-2 weeks
after days and peaks several weeks
several weeks after

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16
Q

degeneration of the descending corticospinal tracts aafter stroke is called

A

wallerian degeneration

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17
Q

most common intercerebral hemorrage cause is

A

hypertention

18
Q

causes superficial lobar hemorrhage

A

cerebral amyloid angiopathy(superficial arteries are most superficial to emboli)

19
Q

berry aneurysm sequelae
both acue and chronic

A

vasospasm in base of the brain
chronic: fibrosis of leptomeningies and hydroencephalus

20
Q

causes of berry aneurysm are

A

smoking and hypertensyion
marfan syn. and PCKD

21
Q

commonest congenital vascular abnormality and mostly seen in males where abnormal connections between veins and , A, are seen = glioti brain tissue between vessels , seizures, migranes

A

AVM

22
Q

recovery with amnesia for the event, no lesion

A

concussion

23
Q

injury of gyri crest, croup and countercroup

A

contousions and lacirations

24
Q

Acceleration / Deceleration injury and Stretching forced that effects the white matter and post-traumatic coma, demintia are seen

A

Diffuse Axonal Injury

25
Q

skull fracture causing Rupture of middle meningeal artery and shows lucid and rapid loss of consciousness

A

Epidural hematoma

26
Q

seen when changed head velocity, Disruption of Bridging Veins and About 50% of acute are accompanied by fracture.
can be Acute (Frontoparietal is common.)

Chronic (develops after 3 weeks, brain atrophy or ‘Battered Baby Syndrome)

A

Subdural hematoma
More common than epidural

27
Q

Level of injury determines outcome:
 Thoracolumbar →
 Cervical →
 Above C4 →

A

Paraplegia

Quadriplegia

Paralysis of diaphragm

28
Q

most common intracranial tumors in adults:

A

metastatic
glioblastoma multiform
anaplastic astroctoma
meningioma

29
Q

most common intracranial tumors in children:

A

astrocytoma
meduuloblastoma
ependymoma

30
Q

ki 67 is a marker of:

A

proliferative marker

31
Q

extraspinal and extradural intraspinal tumors are

A

lymphoma and metastasis

32
Q

extramedullary intraspinal tumors

A

shwannoma and meningioma

33
Q

intramedullary intraspinal tumors

A

epnedymoma and astrocytoma

34
Q

secound most form of dementia after Alzheimer and seen after multiple strokes with grey matter lesions

A

vascular demintia

35
Q

TDP43 mutation and pick bodies
apoptosis , expanded ventricles and shrink in brain

A

FRONTOTEMPORAL DEMENTIAS of picks disease

36
Q

a synuclein gene mutation, with lewy bodies is:

A

parkinson diz and L DOPA is used

37
Q

: Dementia that appears within 1 yr. of onset of motor symptoms,

A

Lewy body dementia

38
Q

autosomal dominant and a defect in ch 4 with CAG repeat and POLYQ
choreforim is seen

A

HUNTINGTON DISEASE

ATROPHY IN STARTUM

39
Q

Accumulation of α synuclein gene product → neuronal death in S.N. producing dopamine → difficulty initiating movement.

with tremor, cogwheel rigidity,slow movements, expressionless facies and instability

A

Parkinson disease

40
Q

genetic mutation on Cha → overproduction of CAG repeats → death of neurons in basal ganglia → Choreiform movements

A

Huntington disease

41
Q

, β amyloid accumulation in and around neurons in the neocortex and hippocampus (control memory) → Death of neurons

A

Alzheimer disease→

42
Q

mutation in superoxide dismutase SOD1
on ch21 \TDP 43

Riluzole is USED T REDUCE FOR 2 -3 MONTHS

A

Amyotrophic Lateral Sclerosis, (ALS) Lou Gehrig’s disease