accumulation Flashcards

1
Q

Diabetes mellitus

A

Glycogen accumulates in renal tubular epithelium , cradiac myocytes and beta cells of the islets in the pancreas.

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2
Q

Glycogen storage diseases

A

Enzymatic defects

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3
Q

Carbon

A

The most common exogenous pigment

In the lung and the hilar lymph nodes

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4
Q

Anthracosis

A

Carbon aggregates in the lung and hilar lymph nodes

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5
Q

Endogenous pigments

A

Lipofuscin, melanin and hemosiderin

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6
Q

an endogenous, brown-black pigment formed by melanocytes.

A

Melanin

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7
Q

represents complexes of lipid and protein that derive from the free radical-catalyzed peroxidation of polyunsaturated lipids of subcellular membranes.

A

Lipofuscin

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8
Q

not injurious to the cell but is important marker of past free radical injury.

A

Lipofuscin

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9
Q

accumulates in tissues when there is a local or systemic excess of iron

represents large aggregates of ferritin

A

Hemosiderin

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10
Q

pigment appears as perinuclear electron-dense granules

“brown atrophy” if apparent grossly

A

Lipofuscin

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11
Q

Affects mainly the interstitium of blood vessels, kidneys, lungs, and gastric mucosa.
Does not generally cause clinical dysfunction, unless the process is severe.

A

Metastatic calcification

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12
Q

in aortic valve is an important cause of aortic stenosis in the elderly

A

Dystrophic calcification

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13
Q

nephrocalcinosis

A

Metastatic calcification

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14
Q

adjacent basal keratinocytes in the skin can also accumulate the pigment (e.g., in freckles), or it may be accumulated in dermal macrophages.

A

Melanin

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15
Q

Haemoglobin derived golden-yellow to brown pigment.

A

Hemosiderin

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16
Q

abnormal deposition of calcium salts, together with smaller amounts of iron, magnesium and other minerals.

A

Pathological calcification

17
Q

Deposition of calcium on dead or dying cells.

Normal levels of serum calcium

A

Dystrophic calcification

18
Q

Wear and tear pigment

A

Lipofuscin

19
Q

Grossly appears as fine white granules.

Microscopically: intracellular or extracellular basophilic deposits.

A

Dystrophic calcification

21
Q

Deposition of calcium in normal tissue in the presence of hypercalcemia.

A

Metastatic calcification

21
Q

Causes of hypercalcemia:

A

Increased secretion of parathyroid hormone.
Destruction of bone by tumors.
Vitamin-D related disorders.
Renal failure.

22
Q

fatty liver

A

Abnormal metabolism of substances

23
Q

alpha-1 antitrypsin deficiency

A

Defective folding and transport of proteins

24
Q

storage diseases

A

Genetic or acquired lack of enzyme

25
Q

Steatosis

A

abnormal accumulation of triglycerides within parenchymal cells

Liver is the most common organ affected, but heart, skeletal muscles and kidney may be affected.
Fatty changes are reversible.

26
Q

Causes of fatty change

A

Toxins: alcohol is the most common cause.
Protein malnutrition: due to decrease in the synthesis of apolipoproteins.
Diabetes mellitus
Obesity
Anoxia and starvation

27
Q

by light microscopy as small fat vacuoles in the cytoplasm around the nucleus.

With accumulation, the organ enlarges and becomes progressively yellow, greasy & soft

A

Fatty change

28
Q

Mainly accumulates in macrophages, leading to the formation of foam cells.

A

Cholesterol and it’s esters

29
Q

give atherosclerotic plaques their yellow color.

A

Cholesterols lipid vacuoles

30
Q

xanthomas

A

In hereditary and acquired hyperlipidemic syndromes, macrophages accumulate intracellular cholesterol; when present in the subepithelial connective tissue of skin or in tendons, clusters of these foamy macrophages form masses called xanthomas.

31
Q

there is an increased pinocytic reabsorption of the protein. Fusion of these pinocytic vesicles with lysosomes results in the histologic appearance of pink, hyaline cytoplasmic droplets

A

nephrotic syndrome

32
Q

accumulation of newly synthesized immunoglobulins within the RER in plasma cells.

A

Russell bodies

33
Q

alcoholic hyaline

A

Mallory bodies

34
Q

accumulation of eosinophilic intracytoplasmic inclusions (prekeratin filaments) in liver cells in alcoholic liver disease.

A

Mallory bodies or “alcoholic hyaline

35
Q

found in the brain in Alzheimer disease; aggregated protein inclusion contains microtubule-associated proteins and neurofilaments.

A

Neurofibrillary tangle