Reversible Cell Injury III

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Last updated 3:52 AM on 7/11/26
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30 Terms

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Secondary amyloidosis

Amyloidosis that is caused by complication of underlying disease

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chronic inflammation

example of secondary amyloidosis

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deep brown, yellow

In detection of amyloid grossly, Lugol’s iodine stains amyloid ______ while normal tissue is color _____

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H&E, homogenous pink, smudgy extracellular material

In using light microscopy as amyloid detection, what stain should we use? and what is it gonna look like?

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Polarizing microscopy

What type of microscopy is used to detect amyloid that uses Congo Red stained section and results in green birefringence?

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fine non-branching fibrils about 7.5-10nm in diameter

In electron microscopy, you’ll see _____ in amyloid positive tissue sample.

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Beta-pleated sheet structure of fibrils

X-ray diffraction

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bladder amyloidosis in congo red staining

what this?

<p>what this?</p>
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Nasal amyloid display in apple green birefringence in polarized light

what this?

<p>what this?</p>
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fibrinoid degeneration/fibrinous degeneration/fibrinoid necrosis

Cellular accumulation characterized as poorly defined, deeply acidophilic, homogenous refractile deposits

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connective tissue, blood vessel walls

fibrinoid degeneration occurs in

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fibrin

some fibrinoid degeneration staining reactions resembles

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  1. phosphotungstic acid haematoxylin (PTAH)

  2. Masson’s trichome

  3. Martius Scarlet Blue

spacial stains of fibrinoid degeneration

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glycogen degeneration

Cellular accumulation characterized as excessive accumulation of glycogen in cells following defective carbohydrate metabolism

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parenchymal cells, liver cells

Glycogen degeneration if seen in _______ particularly in ____

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  • atrophy from malnutrition

  • vacuolar degeneration

associated changes with glycogen degeneration

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<p>PAS on frozen section</p>

PAS on frozen section

special stains of glycogen degeneration

<p>special stains of glycogen degeneration</p>
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<p>mucopolysaccharidosis</p>

mucopolysaccharidosis

Cellular accumulation of mucopolysaccharide , also known as lysosomal storage disease

<p>Cellular accumulation of<strong><u> mucopolysaccharide</u></strong>&nbsp;, also known as<strong><em> lysosomal storage disease</em></strong></p>
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lysosomal enzyme system that breaks glycosaminoglycans 

Basic defect of mucopolysaccharidosis is the absence or loss of critical _________ usually from genetic disorders

<p>Basic defect of mucopolysaccharidosis is the absence or loss of critical _________ usually from genetic disorders</p>
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  • myxoid degeneration

  • myxomatous degeneration

  • mucoid or mucinous degeneration

Old terms of Mucopolysaccharidosis

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Toluidine blue in resin section

Stain of mucopolysaccharidosis

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  • endogenous

  • exogenous

What are the pigment sources of pathological pigmentation?

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  • hemoglobin derivatives (hemosiderin, bilirubin)

  • melanin

  • lipofuscins

under endogenous pigment source

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  • pneumoconiosis

  • anthracosis

under exogenous pathological pigment source

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okie dokie yo

study this diagram pleae

<p>study this diagram pleae</p>
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hemosiderin

Local deposits on tissues denote local breakdown of red blood cells

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hemorrhages and tissue trauma

sample of hemosiderin

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ferritin

storage form of iron that is usually seen in sections of spleen and in bone marrow

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<p>Perls’  prussian blue test</p><p></p>

Perls’ prussian blue test

detections of hemosiderin

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<p>ferrocyanide</p>

ferrocyanide

In Perls’ Prussian Blue Test, ferritin reacts with _____ in the stain to form insoluble Prussian blue dye in situ

<p>In Perls’ Prussian Blue Test, ferritin reacts with _____ in the stain to form <strong>insoluble Prussian blue dye in situ</strong></p>