Pathology Flashcards

(42 cards)

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

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

22
Q

recovery with amnesia for the event, no lesion

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
skull fracture causing Rupture of middle meningeal artery and shows lucid and rapid loss of consciousness
Epidural hematoma
26
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)
Subdural hematoma More common than epidural
27
Level of injury determines outcome:  Thoracolumbar →  Cervical →  Above C4 →
Paraplegia Quadriplegia Paralysis of diaphragm
28
most common intracranial tumors in adults:
metastatic glioblastoma multiform anaplastic astroctoma meningioma
29
most common intracranial tumors in children:
astrocytoma meduuloblastoma ependymoma
30
ki 67 is a marker of:
proliferative marker
31
extraspinal and extradural intraspinal tumors are
lymphoma and metastasis
32
extramedullary intraspinal tumors
shwannoma and meningioma
33
intramedullary intraspinal tumors
epnedymoma and astrocytoma
34
secound most form of dementia after Alzheimer and seen after multiple strokes with grey matter lesions
vascular demintia
35
TDP43 mutation and pick bodies apoptosis , expanded ventricles and shrink in brain
FRONTOTEMPORAL DEMENTIAS of picks disease
36
a synuclein gene mutation, with lewy bodies is:
parkinson diz and L DOPA is used
37
: Dementia that appears within 1 yr. of onset of motor symptoms,
Lewy body dementia
38
autosomal dominant and a defect in ch 4 with CAG repeat and POLYQ choreforim is seen
HUNTINGTON DISEASE ATROPHY IN STARTUM
39
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
Parkinson disease
40
genetic mutation on Cha → overproduction of CAG repeats → death of neurons in basal ganglia → Choreiform movements
Huntington disease
41
, β amyloid accumulation in and around neurons in the neocortex and hippocampus (control memory) → Death of neurons
Alzheimer disease→
42
mutation in superoxide dismutase SOD1 on ch21 \TDP 43 Riluzole is USED T REDUCE FOR 2 -3 MONTHS
Amyotrophic Lateral Sclerosis, (ALS) Lou Gehrig’s disease