BRACE YOURSELF!!! Its about to get rocky!! (Extracellular accumulations)

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80 Terms

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extracellular accumulations

what are all of these?: Hyaline Substances, Amyloid, Fibrinoid Necrosis/Change, Collagen/Fibrosis, Fatty Infiltration, Gout/Pseudogout, Cholesterol, Calcification, Heterotopic Ossification

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hyaline substances

homogenous, eosinophilic, and translucent appearance to a cellular or extracellular substance

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EOSINOPHILIC

Proteins are stained _________ in hyaline substances?

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True

true/false: Hyaline is an ADJECTIVE to describe a substance, but often means theres protein somewhere

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protein in renal tubules, serum/plasma in vessels, collagen fibers, thickened basement membranes, corpora amylacea

What are some examples of hyaline substances?

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Concentric layers of glycoprotein in glands or CNS

Corpora amylacea? Wtf? Define:

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hyaline casts

What extracellular inclusion?

<p>What extracellular inclusion?</p>
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corpora amylacea

What extracellular inclusion?

<p>What extracellular inclusion?</p>
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FALSE; named for it's ability to stain with iodine

true/false: amyloid is named for its "starch like" qualities

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mis-folded proteins

What is amyloid?

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highly ordered, fibrillar polypeptide chains, cross beta sheets, pathogenesis, morphological appearance

Amyloid is: Unfolded or partially unfolded proteins or peptide fragments

They are ___________, generic structure of ________________________

Rich in ______________________

Biochemically diverse with common __________ and ____________________

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true

true/aflse: myloid proteins can self replicate

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self-replicaiting template, failure to degrade, genetic mutations, overproduction from abnormality in synthesizing cell, loss of chaperone molecules in assembly process

There are 5 "causes" of amyloid on slide 10. Read if you want but they're all ways the body screws up proteins; listed VERY generally here:

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precursor peptide/protein

Amyloid types are classified based on the biochemical identity of their _______________________

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immunoglobulin light chains, plasma cells

AL type Amyloid is from __________________ derived from __________

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Primary

is type AL amyloid primary or secondary?

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dyscrasia, neoplasia, light chain fragments

AL is produced by plasma cell _________ or _______________. Where the abnormal plasma cells secrete the _________________ into circulation

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serum amyloid A protein, hepatocytes, high-density lipoproteins

Type AA amylase, is a ________________________ produced by ________________ and bound to ____________________ in circulation

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secondary; associated with other proteins

is Amyloid type AA primary or secondary?

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Chronic inflamation!!! (AL is typically more localized)

Type AA amyloid is more associated with ________________

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true

true/false: Amyloid type AA can have Hereditary or familial forms also recognized like in Shar-Pei dogs and Abyssinian cats

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renal glomeruli, liver, spleen

AA amyloid is classically where?

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read.

Read pls: (sorry) AA amyloid process:

taken up by cells and converted from alpha-helical confirmation to beta-sheets → forms oligomers that disrupt cell membranes and leave the cell → oligomers form fibrils that aggregate in deposits → disrupt tissue function

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disrupts and damages

Deposition of amyloid ______- and ______________ tissues

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systemic

what type of amyloid is Amyloid deposited around the body in multiple organs

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localized

what type of amyloid is amyloid deposition restricted to tissues which produce the precursor protein or peptide

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systemic

is systemic or localized amyloid more likely to be life threatening?

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localized

These are both examples of what type of amyloid?

Islet amyloid peptide secreted by beta cells in pancreatic islets in cats

Beta-amyloid in cerebral cortex of aged dog with canine cognitive dysfunction

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amyloid

describe the extracellular inclusion

<p>describe the extracellular inclusion</p>
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amyloid

describe the extracellular inclusion

<p>describe the extracellular inclusion</p>
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Congo red stain

what stain is uniquely associate with Amyloid inclusions?

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apple green biferingence under polarized light

Congo red is orange-red on origional staining... but then you do something special to it. What does it look like and in what special conditions?

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Firm, yellow, waxy, coalescing nodular or amorphous deposits

describe amyloid grossly

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iodine, sulfuric acid

you pan amyloid lesions with ______ to get a yellow color, add _______ to get blue violet

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conjunctival amyloidosis

Describe this lesion

<p>Describe this lesion</p>
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AA

Which type of amyloid?

<p>Which type of amyloid?</p>
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Fibrinoid necrosis

Type of extracellular change from the leakage of plasma proteins into the vessel wall

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true

true/false: fibrinoid necrosis is related to inflammation, infection, trauma, or other injury

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fibrinoid necrosis change

describe the extracellular accumulation

<p>describe the extracellular accumulation</p>
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fibrosis

_________: excess in fibrous collagen (type I collagen) in the interstitium

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fibroblasts, injury or inflammation

collagen/fibrosis is typically produced by __________________ after _________________ or ____________

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scarring

collagen/fibrosis can also be present in ____________ that may compromise organ function

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myocardial fibrosis

Describe this extracellular inclusion (heart muscle)

<p>Describe this extracellular inclusion (heart muscle)</p>
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fatty infiltration

_______________: Increase in the number and/or volume of adipocytes in the interstitium of an organ or tissue due to obesity, cardio- or skeletal myopathies, or atrophied tissue

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fatty infiltration

Describe the extracellular accumulation (this is a heart muscle)

<p>Describe the extracellular accumulation (this is a heart muscle)</p>
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gout

________: deposition of sodium urate crystals (urates) in tissues

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birds, reptiles

gout is most commonly seen in animals in _______ and _______

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pseudogout

___________________: deposition of calcium pyrophosphate crystals in tissues

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tophi

What is the specific term for the inflammatory response ellicited from neutrophils/heterophils and macrophages by gout

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articular, visceral

What are the two types of gout?

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renal gout tophi

Describe this extracellular inclusion in the kidney

<p>Describe this extracellular inclusion in the kidney</p>
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cholesterol

_______________ crystals can form at sites of hemorrhage or necrosis but dissolve during processing, forming acicular clefts seen in histologic sections

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macrophages

what do cholesterol crystals attract?

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cholesterol

what is this extracellular inclusion?

<p>what is this extracellular inclusion?</p>
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pathological calcification

____________________: deposition of calcium salts in soft tissues

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metastatic calcification

type of calcification as the result of hypercalcemia

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calcium and phosphorus

Metastatic calcification occurs as the result of an imbalance of _______ and _________

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Primary hyperparathyroidism, Renal secondary hyperparathyroidism, Hypervitaminosis D (plant toxicosis, rodenticides), Paraneoplastic syndromes

What are some causes of metastatic calcification

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intima, tunica media, basophilic stippling

Microscopically, metastatic calcification looks like deposits in the _______ and _________ of vessels, with a subtle ________________

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von kossa, the silver in it stains the calcium salts black

What is the specific stain associated with calcium? How does it work?

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gastric calcification

Describe this extracellular inclusions?

<p>Describe this extracellular inclusions?</p>
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Von kossa staining

this is calcification... why does it look like that?

<p>this is calcification... why does it look like that?</p>
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gritty white ish granules or streaks

Describe mestastatic calcification grossly

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Metastatic calcification

what would make this aorta look like that?

<p>what would make this aorta look like that?</p>
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dystrophic calcification

type of calcification of dead tissue as part of necrosis

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loss of Ca balance during cell injury

What is the machanism for dystrophic calcification?

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mitochondria, ER, cytosol

where is caclium sequestered in a healthy cell

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white muscle disease

what is dystrophic calcification in striated muscle called? (from vitamin E/Se deficiency

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necrosis, repetitive trauma

what are the main causes of dystrophic calcification?

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basophilic stippling, mitochondria, basophilia

Dystrophic calcification is initially visible as _________ most profoundly in the [what organelle]. But then progresses to the whole cell and extracellular tissue as widespread intense ______________

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dystrophic calcification

this is actually a caseous necrosis, but how would you describe the extracellular inclusions?

<p>this is actually a caseous necrosis, but how would you describe the extracellular inclusions?</p>
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gritty white ish granules or streaks

describe dystrophic calcification grossly

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dystrophic calcification

describe what extracellular inclusion you would expect to see with this lesion

<p>describe what extracellular inclusion you would expect to see with this lesion</p>
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dystrophic

is this dystrophic or metastatic?

<p>is this dystrophic or metastatic?</p>
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heterotropic ossification

______________: formation of bony tissue at an extra-skeletal site

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in chronic lesions of soft tissue calcification

Where do you find Heterotropic ossification?

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False; does not always ossify

true/false: Pathological calcification, given enough time, will always calcify

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hard spicules or nodules

What does heterotropic ossification look like grossly?

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in lungs and dura of old dogs

Heterotrophic ossification can be an incidental finding on necropsy... for example, in:...

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Dural ossification

What is this extracellular inclusion of the dura mater?

<p>What is this extracellular inclusion of the dura mater?</p>