Introduction Flashcards

0
Q

hypertrophy (n.)

A

an increase in cell size, accompanied by increased functional capacity

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1
Q

hyperplasia (n.)

A

an increase in the number of cells in an organ or tissue

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2
Q

metaplasia (n.)

A

replacement of a tissue with another normal cell type

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3
Q

atrophy (n.)

A

a decrease in cell size and differentiated function

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4
Q

dysplasia (n.)

A

metaplastic cells that begin to function abnormally, often preneoplastic; occurs when chronic injury persists

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5
Q

carcinoma in-situ (n.)

A

All cells of the tissue have been replaced by dysplastic cells, but have not invaded adjacent tissues

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6
Q

What was the average lifespan of Neolithic humans?

A

20-25 years

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7
Q

Where is an abnormal accumulation of fat most often found?

A

The liver

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8
Q

calcification (n.)

A

calcium entry into dying or dead cells occurs due to steep gradient across the plasma membrane (10K times greater extracellularly)

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9
Q

What happens normally to free fatty acids?

A

They’re taken up by liver and oxidized/converted to TG

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10
Q

dystrophic calcification (n.)

A

macroscopic deposition of calcium salts in injured tissues

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11
Q

What does dystrophic calcification require to occur?

A

Persistent necrotic material

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12
Q

What is one way to detect dystrophic calcification?

A

Detected by mammography when breast cancer is present

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13
Q

When will there be dystrophic calcifications in the brain?

A

Congenital toxoplasmosis

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14
Q

metastatic calcification (n.)

A

deranged calcium metabolism; a systemic process

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15
Q

Where are common places of calcium deposition in hypercalcemia?

A

Alveolar septa of lung, renal tubules, blood vessels

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16
Q

What is found in the lungs and regional lymph nodes in anthracosis?

A

Carbon particulates (normal)

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17
Q

Where are tattoos stored and what are they made of?

A

Insoluble metal and vegetable pigments that are engulfed by dermal macrophages and persist

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18
Q

What metal is deposited in Wilson’s disease, and where?

A

Excess copper is deposited in the liver, brain, and cornea

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19
Q

Where is iron stored?

A

Stored in proteins called ferritin in the liver and bone marrow

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20
Q

hemosiderin (n.)

A

partially denatured ferritin that aggregates easily; found in bone marrow, spleen, and Kuppfer cells

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21
Q

Kuppfer cells (n.)

A

liver macrophages

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22
Q

What causes hydropic change, cellularly?

A

Intracellular accumulation of Na+, leading to excess water in the cell

23
Q

When does necrosis occur?

A

When the barrier function of the plasma membrane is breached; usually associated with a strong inflammatory response

24
apoptosis (n.)
programmed cell death, due to extra- or intracellular signals
25
What types of lymphocytes induce apoptosis?
NK cells and cytotoxic T cells
26
karyolysis (n.)
fading away of the nuclear envelope
27
pyknosis (n.)
shrinking up and condensing of the nuclear envelope
28
karyorrhexis (n.)
break up of nuclear envelope
29
What is the morphology of coagulation necrosis?
Normal tissue architecture essentially maintained
30
When/where does coagulation necrosis often occur?
Myocardium after an infarct
31
What is the morphology in liquefaction necrosis?
Relative lack of connective tissue, due to enzyme digestion
32
coagulation necrosis (n.)
cell death due to loss of circulation
33
What is liquefaction necrosis often called in an infected limb?
Gangrenous necrosis
34
Where do we see liquefaction necrosis?
In the foci of bacterial/fungal infections, in the CNS, in infected limbs
35
What is the morphology of caseous necrosis?
Cheesy, white gross appearance of the central necrotic area
36
Where is caseous necrosis most often encountered?
Lungs infected with tuberculosis
37
What is the morphology of fat necrosis?
Focal areas of fat destruction
38
Where is fat necrosis often seen?
Pancreatic injuries
39
What is the normal tissue type in respiratory airways?
Pseudostratified ciliated columnar epithelium
40
What causes Barrett's esophagus?
Lots of acid reflux into the esophagus
41
What is Barrett's esophagus?
Metaplasia of stratified squamous in esophagus to simple columnar; preneoplastic
42
What can cause spastic paralysis?
Upper motor neuron damage
43
What can cause flaccid paralysis?
Lower motor neuron damage
44
xanthelasmas (n.)
accumulations of cholesterol in skin lesions
45
What are the five types of abnormal proteins we study in accumulations?
prions, Lewy bodies, alpha1-antitrypsin, neurofibrillary tangles, and Mallory bodies
46
Abnormally folded prion proteins are present in __________. (2 words)
spongiform encephalopathies
47
What protein inclusions are found as a result of alcoholic livery injury?
Mallory bodies
48
What are found in the cortical neurons of Alzheimer's disease?
neurofibrillary tangles (tau proteins)
49
Where does alpha1-antitrypsin accumulate in a deficiency?
Hepatocytes, which leads to cirrhosis
50
What disease is caused by a Lewy body accumulation?
Parkinson's disease
51
Where do Lewy bodies accumulate in people with PD?
The neurons of the substantia nigra
52
What are Lewy bodies composed of?
alpha-synuclein
53
atherosclerosis (n.)
the hardening of arteries
54
Where are lipofuscin granule accumulations found?
myocardium, neurons, and liver
55
Where is hyaline change found?
damaged arterioles, renal tubules, damaged liver cells, and neurons