MBB Pathology/Imaging Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

Describe what you see here; what condition is this

A

rounded atrophic fibers and lymphocytic infiltrate; top right is macrophages attacking muscle fiber; polymyositis

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

describe the constellation of findings seen and for what disease

A

a) balooning neuron

b and c) neurofibrillary tau tangles

d) astrocytic plaques

corticobasal degeneration

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

Describe the difference between hemorrhagic infarct and a intraparenchymal hemorrhage and how they would look micro/macroscopically

A

Hemorrhagic infarct has brain tissue with blood infiltrating, tissue is becoming necrotic, wil lsee petechiae and neutrophils etc.

intraparenchymal hemorrhage is when blood spills out and pushes brain tissue out of the way and takes up space, so microscopically you would only see blood and fibrin

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

what is this

A

medulloblastoma

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

What is going on here, what is causing it

A

central herniation of temporal lobes, brainstem bein displaced downward, severing basilar pontine arteries, fatal (overall cause is edema)

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

What is going on in this image? what condition is this common in

A

asymmetrical atrophy; corticobasil degeneration

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

What is this? What conditions is this common in

A

lewy bodies, Parkinson’s disease, Lewy body dementia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is this, what is the most common cause, is it fast or slow growing

A

subdural hemorrhage, trauma, slow growing

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

describe what you see; what condition is this common in

A

ballooned neuron; corticobasil degeneration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Name 3 possible causes of this

A

high grade glioma (GBM)

cns lymphoma

rlly bad MS

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

describe what you see; what type of cancer is this; what age group is involved

A

dense eosinophilic rosenthal fibers; pilocytic astrocytoma children

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

Describe the process going on here from left to right and what kind of process is this?

A

myopathic process

1) left most: muscle fiber necrosis
2) middle: attempts at regeneration
3) fibrosis

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

What is going on here; what condition would this be seen in

A

alpha synnuclein cytoplasmic inclusions in GLIAL cells; multiple system atrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are yo ustaining for here; what disease is this common in

A

staining for ubiquitin/huntington protein inclusions ; huntington disese

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

describe what you see; what disease is this

A

neuronal loss, reactive (alzheimers type 2 ) astrocytes; metabolic gliosis (thing in the center) –> wilson’s disease

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

what cancer is this

what demographic is it common in

A

medulloblastoma children

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

describe the symptoms; what syndrome do they belong to

A

plexiform neurofibroma on peripheral nervous sytem

cafe au lait spot

neurofibromatosis 1

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

What is this? Name some causes?

A

interparenchymal hemorrhage, htn most common, also arteriovenous malformation, lesion, amyloid

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

describe the two images; what condition is this

A

swollen neuron aka pick cell

status spongiosis aka vacuolization of the cortex

pick’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what is this, where does it come off of

A

vestibular schwannoma/acoustic neuroma; nerve VIII at the cerebellopontine angle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

describe what yo usee; what cancer is this

A

vascular tumor, vacuolated stroma, hemangioblastoma from von hippel lindau

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Describe these findings; what condition is this associated with

A

different manifestations of tau protein accumulations

left is neurfibrillatory tangles

bottom left is tufted astrocytes

right (c shpaed) is glial inclusions (also neuronal inclusions)

PROGRESSIVE SUPRANUCLEAR PALSY

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Describe what is happening here: what condition is this

A

perifascicular atrophy; dermatomyositis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

describe each of the three images; what disease is this

A

top- cerebral amyloid angiopathy (amyloid depositing in leptomeningeal and intraparenchymal arteries)

bottom left- granulovaculoar degeneration (clear cytoplasmic inclusions with basophilic granules)

bottom right- hirano bodies, glassy eosinophilic bodies made of actin

alzheimers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What virus is responsible for this? what is happening

A

polio virus; microglia are surrounding a dying neuron and trying to eat it (neuronophagia, microglial nodule)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

what are these; what condition is it common in

A

glial cytoplasmic inclusions, multiple system atrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

describe what you see; what condition is this

A

rounded atrophic fibers, lymphocytic infiltrate; purple cytoplasmic vacuolar inclusions; inclusion body myositis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

what do you see; what is it called; what conditions is this associated with

A

acellular region then pallisating region, verrucay bodies; schwannoma and neurofibromatosis 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

describe what you see on the left and bottom right image; what are they called; what condition are they common in

A

left: dense eosinophilic center with clearing around it, lewy body
right: lewy neurites

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What process is going on here for what disease

A

in parkinsons alpha synnuclein can accumulate so much that the neuron dies and then this image shows microglia coming in to eat the dead neuron

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

What type of astrocytoma is this ? how do yo uknow

A

diffuse, only hypercellcularity and atypia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

describe what you see

A

diffuse enhancing lesion; lymphoid cells

cns lymphoma

33
Q

What neuropathy causes this? why does this happen

A

radial nerve neuropathy; loss of extension of the fingers and wrist

34
Q

what is going on here; what condition is this

A

atrophic muscle fibers and a few normal/hypertrophic fibers; werdnig hoffman disease/spinal muscular atrophy

35
Q

What is happening here; what condition is this

A

onion bulb; attempt at remyelination after demyelination (right pick has schwann celsl surrounding); chronic inflammatory demyelinating polyneuropathy

can also happen in charcot marie tooth

36
Q

Describe what you see; what cancer is this and what condition can this occur

A

large astrocytes in sheaths, subepyndemal lgiant cell astrocytoma (SEGA); tuberous sclerosis

37
Q

what is the arrow pointing to? wha is it made of what condition is this

A

bunina body, tdp43, amyotrophic lateral sclerosis

38
Q

describe what you see; what is this

A

cystic; pilocytic astrocytoma

39
Q

describe what you see; what hiv associated condition is this

A

calcifications; toxoplasmosis

40
Q

what type of hemorrhage is this

what condition is commonly associated with this and what age group

A

lobar hemorrhage, amyloidosis, old people

41
Q

what neurodegenerative disease is this? what are these called

A

pick’s disease; pick bodies made up of tau 3r

42
Q

Describe what you see, what is this called, what can cause this

A

optic disc borders aren’t sharp, blood vessels runcated; papilledema; increse intercanial pressure due to brain tumor

43
Q

What type of astrocytoma is this ? how do yo uknow

A

gbm; has pseudopalisating necrosis and endothelial proliferation

44
Q

What neuropathy causes this? Why do the fingers look like this

A

ulnar nerve neuropathy; inability to flex MCP (lumbricals) and inability to extend IP (interossei)

45
Q

what is this called? what group of disorders is this common in

A

ragged red fibers (accumulation of abnormal mitochondria), mitochondrial myopathies

46
Q

Describe what you see

what tumor is this

what population is affected

what symptoms would yo uexpect

A

small blue cells, high nuclear to cytoplasmic ratio, can be arranged n lines, can have homer wright rosettes; can have drop mets

medulloblastoma; homer wright rosettes

47
Q

What are the signs of what the arrows are pointing to; what is it indicative of

A

insular ribbon sign and hyperdense MCA sign; infarct of MCA

48
Q

what is this called? What condition is this common in

A

hummingbird sign (midbrain atrophy), progressive supranuclear palsy

49
Q

What kind of rash is this; what is this common in? what else can concomittantly happen with this

A

maculopapular rash, neisseria meningitidis, DIC and thrombocytopenia

50
Q

what do you see; what cancer is this

A

basiloid cells surrounding a cyst

wet keratin (pink)

purle= calcifications

carniopharyngioma

51
Q

Describe each of the three images, what staining it is and whether they belong to a certain condition

A

top left= normal staining for dystrophin (brown)

top right: staining for duchenne muscular dystrophy; no dystrophin is present

bottom right: staining for becker muscular dystrophy, reduced dystrophin is present

52
Q

what are the triangular shaped blobs; what is wrong with this pic; what condition is this

A

neurons; loss of neurons; als

53
Q

what type of tumor is this

how can you tell

A

meningioma, dural tail, hyperostosis

54
Q

what type of astrocytoma is this? how do you know?

A

anaplastic, has mitoses

55
Q

Describe whaty you see; what condition is this seen in? what else coudl you stain for

A

neuronal loss and subsequent astrocytosis (small purple things); huntington’s disease; can also stain ubiquitin to look for huntington protein inclusions, but not really necessary

56
Q

What part of the body is this? what is happening

A

muscle, angulated atrophic fibers on the left, nuclear cluster on the right (due to atrophy of the muscle, nuclei are now closer together); denervation injury

57
Q

what are C and U; what is different about them, what condition is this

A

lateral and anterior corticospinal tracts; demyelinated; ALS

58
Q

what is going on here; what condition is this

A

lipid accumulation in the muscle fibers: carnityl palmitoyl transferase deficiency

59
Q

What is this? what most commonly causes this? is it fast or slowly growing?

A

epidural hematoma, trauma to middle meningeal artery, fast growing

60
Q

describe what you see ; What type of cancer is this?

A

cuboidal to elongated ependymal cells surrounding a stromal core; myxopappilary ependymoma

61
Q

describe what you see; what hiv associated condition is this

A

enahncement of basal ganglia with sparing of thalamus; cryptococcus meningitis

62
Q

what is this called; what imaging modality is this; what condition is this common in

A

hot cross bun sign (in pons); mri; multiple system atrophy

63
Q

describe the two pictures, which cancer is this, what population is it most common in

A

whorling pattern and psamomma bodies; meningioma, older women (can be associated in chidlren if NF2 Chromosome 22q)

64
Q

What i happening here; what condition is this

A

glycogen filled muscle fibers; myophosphorylase deficiency, can stain with PAS; mcardle’s

65
Q

describe the muscle on the left vs the muscle on the right. what condition is this

A

left is mroe normal, right is atrophic; amyotrophic lateral sclerosis

66
Q

What are the two types of pathology in this image nd for what disease

A

diffuse plaque top (no neurites around)

neuritic plaque bottom (amyloid center with dystorphic neurites around)

alzheimers

67
Q

what is this? what is the most common cause

A

subarachnoid hemorrhage, aneurysm (a. comm artery and p comm artery most common)

68
Q

What neuropathy causes this and why?

A

median nerve neuropathy; inability to flex 1 and 2 fingers (lumbricals)

69
Q

describe the abnormality seen here

what cancer is this

A

perivascular pseudorosette

ependymoma

70
Q

Describe what is happening; what is the condition

what age group is this common in

A

arteries and veins in clsoe proximity with brian tissue in between; arteriovenous malformation, dangerou

young women

71
Q

What is this before and after pictures showing?

A

loss of axons in diabetic neuropathy

72
Q

what do you see

what is this

A

fried egg= oligocytes

oligodendroglioma

73
Q

What do you see; what is this

A

loss of grey white matter interface, edema, mass effect; hSV encephalitis

74
Q

what is this

A

meningioma

75
Q

what type of neurodegenerative disease is this associated with

A

alzheimers, neurfibrillatory tangles

76
Q

What part of the brain is this? what is change d from the normal view; what disease is this implicated in

A

dark= locus ceruleus, right picture it is less, parkinson’s disease

77
Q

What is happening here; what condition is this common in

A

atrophy of the caudate; huntingtons

78
Q

describe the constellation of findings; what disease is this

A

decreased substantia nigra, discoloration of putamen; multiple system atrophy

79
Q

describe this; what is the only condition this can be

A

cytoplasmic tdp 43 accumulations (should be nuclear)- frontotemporal dementia with tdp43 pathology