Neuropatology Flashcards

1
Q

Peripheral nerves can be a common location of complications from

A

DM

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2
Q

The pathologic lesion is thought to arise from

A

Microvascular injury

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3
Q

Common nerve conditions include 3rd nerve palsy, mononeuropathy multiplex, diabetic amyotrophy, and autonomic neuropathy

A

Diabetic Neuropathy

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4
Q

Conseqences include herniation through openings between brain regions including under the falx cerebri, across the tentorium cerebelli, or through the foramen magnum

A

Cerebral Edema

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5
Q

Linear pontine hemorrhages seen almost exclusively in downward herniation through tentorium cerebelli

A

Duret Hemorrhage

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6
Q

When there is no division of the cerebral hemispheres

A

Alobar holoprosencephaly

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7
Q

The problem appears to be in signalling of developmental proteins in the Sonic Hedgehog pathway in the embryonic face/brain region, so that midline structures are malformed, including the normal midline split of the developing cerebrum into two hemispheres

A

Alobar holoprosencephaly

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8
Q

A cephalic disorder in which the single prosencephalic vesicle fails to split into two hemispheres

A

Holoprosencephaly

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9
Q

Manifests with little apparent damage in neuroimaging studies, but lesions can be seen with microscopy techniques post-mortem

A

Mild diffuse axonal injury

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10
Q

Virtually always the result of a trauma that causes a tear in the middle meningeal artery

A

Epidural Hematoma

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11
Q

Dural vessels—especially the middle meningeal artery— are vulnerable to

A

Epidural hematoma

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12
Q

Patients may be lucid for several hours before symptoms develop

A

Epidural hematoma

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13
Q

Manifest within 48 hours with localizing or (more often) non-localizing symptoms

A

Subdural hematoma

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14
Q

Pyramidal cells of the hippocampus and Purkinje cells of the cerebellum are the most susceptibel neurons for infarcts from

A

Global Ischemia/Hypoxia

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15
Q

Wedge-shaped infarcts in regions perfused by most distal portions of arteries

-Usually seen after hypotensive episodes

A

Watershed (Borderzone) Infarcts

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16
Q

From cerebral arterial occlusion. Less damaging in areas of collateral circulation

A

Infarcts from cerebral ischemia

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17
Q

Can be ischemic (bland, white, common; thrombolytic therapy possible), hemorrhagic (less common; thrombolytic therapy counterindicated), or “transformed” into hemorrhagic (unclear incidence)

A

Infarcts

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18
Q

Hemorrhages involving the basal ganglia area (the putamen in particular) tend to be non-traumatic and caused by

A

Hypertension

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19
Q

Causes hyaline arteriolar sclerosis of the deep penetrating arteries/arterioles supplying the basal ganglia, hemispheric white matter, and brain stem

A

Hypertension

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20
Q

Small (a few millimeters) cavity infarct in the deep gray matter (basal ganglia and thalamus), internal capsule, deep white matter, and pons

A

Lacunar Infarct

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21
Q

Due to occlusion of a small deep penetrating artery as a consequence of aging, hypertension, smoking, and diabetes mellitus

A

Lacunar Infarct

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22
Q

A ruptured berry aneurysm with subarachnoid hemorrhage leads to sudden onset of an excruciating

A

Headache

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23
Q

90% occur in the anterior circulation near major branch points

A

Saccular Aneurysms

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24
Q

1/3 of cases of ruptured saccular aneurysms come from an acute increase in

A

Intracranial Pressure

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25
What 4 things does the CSF show for acute bacterial meningitis?
1. ) Increased opening pressure 2. ) Abundant Neutrophils 3. ) Elevated Protein 4. ) Reduced Glucose
26
Granulation tissue that becomes dense fibrosis over time
Wall of brain abscess
27
Almost always from bacterial infection -Hematogenous spread, often from heart, lungs, distal bone, tooth extraction
Brain Abscess
28
What are the three characteristics of CSF in a brain abscess case?
1. ) Increased white cells 2. ) Increased Protein 3. ) Glucose is normal
29
Most common in children and young adults, with alterations in mood, memory, and behavior
HSV-encephalitis
30
Thought to be due to retrograde transmission from a peripheral to a central location along a cranial nerve
HSV-Encephalitis
31
An umbrella term for different neurological disorders associated with HIV infection and AIDS, including mild to severe dementia
HIV-Associated Neurocognitive Disorder (HAND)
32
Activation of macrophages and microglia is a characteristic of
HIV
33
Characteristic pathologic feature is the microglial nodule with the macrophage-derived multinucleate giant cell
HIV encephalitis
34
The virus travels along peripheral nerves at the wound site to the central nervous system -So incubation period depends on the distance of the wound from the brain
Rabies (w/ Negri Body)
35
Manifests with nonspecific headache, malaise and fever
Rabies
36
Then shows extraordinary CNS excitability including HYDROPHOBIA
Rabies
37
The vacuoles in CJD represent swollen dendrites that are generally close to neuronal cell bodies, and this is the site of much of the abnormal
Prion Protein
38
A sporadic (85% of cases), transmissible, or hereditary disease with rapidly progressive dementia -Death in 7 Months
CJD
39
CJD is “Spongiform” because the cerebral cortex and deep gray matter become riddled with microscopic
Vacuoles
40
A very large indicator of MS is CSF presence of
IgG antibodies
41
An autoimmune demyelinating disease with multiple neurologic deficits at different times due to white matter lesions spatially distinct
MS
42
Usually relapsing and remitting episodes of neurologic impairment -Subset of patients steadily deteriorate
Multiple Sclerosis (MS)
43
Primarily a white matter disease with multiple plaques, though axons may be numerically reduced -Probable central role for CD4+ T-cells
MS
44
The characteristic microscopic findings of Alzheimer’s disease are neuritic plaques and
Neurofibrillary Tangles
45
Neuritic plaques are formed from a central core of neurotoxic extracellular
AB protein
46
One of the neurodegenerative diseases characterized by degeneration of neurons related by function rather than by location in the brain
Alzheimer's Disease (AD)
47
Cleavage of amyloid precursor protein (APP) yields beta amyloid (Ab), which accumulates and injures neurons in
AD
48
An additional risk factor for AD is an apoprotein called
ApoE4
49
A syndrome with diminished facial expression, stooped posture, slowness of voluntary movement, festinating gait, rigidity, and a “pill-rolling” tremor
Parkinsons Disease
50
Due to damage to the nigrostriatal dopaminergic system
Parkinson's disease
51
Parkinson's has characteristic neuronal inclusions of a-synuclein called
Lewy Bodies
52
At autopsy the brain shows pallor of the substantia nigra and the locus ceruleus
Parkinson's
53
The pallor is due to loss of the pigmented
Catelcholaminergic neurons
54
Symptomatic treatment with L-DOPA therapy does not
Halt disease progression of PD
55
A neurodegenerative disease with loss of both lower motor neurons and upper motor neurons
ALS
56
Characterized by muscle denervation and atrophy, weakness, and fasciculations
LMN loss in ALS
57
Characterized by paresis, hyperreflexia, and spasticity and degeneration of the corticospinal tracts
UMN loss in ALS
58
Usually begins in the 5th decade with subtle asymmetric distal extremity weakness
ALS
59
A syndrome with abrupt onset of confusion, abnormal eye movements, and ataxia
Wernicke-Korsakoff
60
Pathologically there are foci of hemorrhage and necrosis in the mammillary bodies and adjacent to the ventricles
Wernicke-Korsakoff
61
High grade with dense cellularity and much nuclear pleomorphism and mitoses
Anaplastic Astrocytoma
62
Same histologic appearance as an anaplastic astrocytoma plus necrosis and vascular proliferation
Glioblastoma
63
Viable cells often form “pseudo-palisades” around vessels (radially-oriented rows of nuclei)
Glioblastoma
64
A mostly benign, well-defined, dura-based mass that may compress the subjacent brain
Meningioma
65
Most separate easily from underlying brain, but some are infiltrative -Arise from arachnoid meningothelial cells
Meningioma
66
Mostly carcinomas—account for ¼-½ of intracranial tumors -80% from primaries in lung, breast, skin (melanoma), kidney, and GI tract
Brain Metastasis
67
Form well-delineated masses, frequently at the grey-white junction, and often produce edema
Brain Metastasis
68
Benign, encapsulated peripheral nerve tumor arising from Schwann cells
Schwannoma
69
Appears as a circumscribed mass abutting an adjacent nerve, usually without involvement of axons
Scwannoma
70
May affect the vestibular portion of the 8th cranial nerve leading to hearing loss
Schwannoma
71
Mostly sporadic but 10% are associated with familial neurofibromatosis type 2
Schwannoma