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CHAPTER 1 11/23/2019 1 SECTION 2 CELL INJURY [email protected]

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CHAPTER 1

11/23/2019 1

SECTION 2 CELL INJURY

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◆Reversible

◆ Irreversible

Cellular Swelling

Fatty Change

Hyaline Change

Amyloid Change

Mucoid Change

Pathologic Pigmentation

Pathologic Calcification

Cell Death

Degeneration

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Reversible Cell Injury

Intracellular &/or extracellular abnormal

accumulation:

⚫ Excess amounts of various normal

substances (water,lipids,proteins,pigments)

⚫ Abnormal substances (exogenous,

endogenous)

Degeneration

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Cellular Swelling

Intracellular accumulation

⚫ Sodium

⚫ Water

(hydropic degeneration)

(1)

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Cellular Swelling (2)

Morphology

NE:

LM:

EM:

⚫ Cloudy swelling

⚫ Increase in the weight

the organs

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Cellular Swelling (3)

Morphology

NE:

LM:

EM:

⚫Large

⚫Small & fine granules in the cytoplasm

the cells

Ballooning change

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Cellular Swelling (4)

Morphology

NE:

LM:

EM:

Swelling

⚫ Endoplasmic reticulum

⚫ Mitochondria

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Injurious agents

Mitochondria damage

Mechanisms

Water & sodium

within the cells

Cellular swelling

ATP

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Fatty Change

Intracellular abnormal accumulation:

⚫ Triglycerides

(1)

Steatosis

Often occurred in the liver and the heart

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Morphology

Fatty Change (2)

NE:

LM:

EM:

⚫ Large

⚫ Yellow

⚫ Soft

⚫ Greasy

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Morphology

Fatty Change (3)

NE:

LM:

EM:

⚫ Round, clear vacuoles

⚫ Orange-red color by staining with

Sudan Ⅲ or Oil Red O (Frozen tissue

sections!)

Fat vacuoles

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Morphology

Fatty Change (4)

NE:

LM:

EM:⚫ Membrane-bound inclusions

Liposomes

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Fatty Change of the Liver

◆ Mild fatty change:

Not affect the gross appearance

◆ With progressive accumulation:

NE

⚫ Large

⚫ Yellow

⚫ Soft

⚫ Greasy

Fatty Liver: Severe & diffuse fatty change

(1)

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Fatty liver

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LM

Fatty Change of the Liver (2)

Fat vacuoles

Small , in the cytoplasm

around the nucleus

Displacing the nucleus

to the cell periphery

Fatty cysts

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CHAPTER 1

11/23/2019 16Fatty change of the liver

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Fatty change of the liver(Sudan Ⅲ)[email protected]

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Mechnisms

Fatty Change of the Liver (3)

⚫Overproduction of triglycerides

⚫Excessive entry of free fatty acids into liver

⚫Enhanced fatty acid synthesis from acetate

⚫Decreased fatty acid oxidation

⚫Decreased apoprotein synthesis

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Fatty Change of the Myocardium

◆ Mild fatty change:

Not affect the gross appearance

◆ With progressive accumulation:

NE

Tigered effect

Apparent bands of yellowed myocardium

alternating with bands of

dark,red-brown,uninvolved myocardium

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Fatty change

of heart

muscle

(tigered effect)

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Fatty change of

heart muscle

(tigered effect)

Sudan-

hematoxylin

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A homogeneous, translucent, pink

appearance in HE staining

Hyaline Change

Intracellular or extracellular abnormal

accumulation:

⚫ Proteins

A descriptive morphologic term

(1)

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◆ Hyaline change in arteriolosclerosis

e.g. Hypertension, Diabetes

◆ Hyaline change in connective tissues

e.g. Old scars

◆ Hyaline change within the cytoplasm

e.g. Nephrotic syndrome, Russell

bodies, Mallory body

Hyaline Change (2)

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Vascular pathology in hypertension. A, Hyaline arteriolosclerosis. The

arteriolar wall is hyalinized, and the lumen is markedly narrowed. [email protected]

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Chronic [email protected]

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Protein reabsorption droplets in the renal tubular epithelium

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Mallory bodies in liver cells

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Amyloidosis

Extracellular abnormal accumulation:

⚫ Amyloid

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Physicochemical characteristics of amyloid

◆ +Iodine--- a brown color--- +H2SO4 --- blue

◆ Staining: Congo red--- red,

HE--- homogeneous pink

◆ EM: nonbranching fibrils 7.5-10 nm wide

◆ X-ray: a pleated –sheet structure

(rendering protein very resistant to

enzymatic degradation, contributing

to its accumulation in tissues)

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Mucoid Change

Extracellular abnormal accumulation:

⚫ Mucopolysaccharide

(Glycosaminoglycans, Hyaluronic Acid)

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Pathologic Pigmentation

Intracellular & extracellular abnormal

accumulation:

⚫ Exogenous

⚫ Endogenous

Colored substances

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Pathologic Pigmentation

⚫ Exogenous

⚫ Endogenous

✓ Hemosiderin

✓ Lipofuscin

✓ Melanin

✓ Carbon

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Carbon

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Hemosiderin granules in macrophages in the alveolus

Hemosiderin

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Hemosiderin granules in liver cells. A, H&E B, Prussian blue reaction

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Lipofuscin

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Melanin

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Pathologic Calcification

Intracellular & extracellular abnormal

accumulation:

⚫ Calcium salts

1. Except for the bones and teeth

2. Pathologic conditions

(1)

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Metastatic calcification in the wall of the stomach

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◆ Dystrophic Calcification

In areas of necrosis

No calcium metabolic derangements

◆ Metastatic calcification

In normal tissues

Some calcium metabolic derangements

Pathologic Calcification (2)

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2. Apoptosis

1. Necrosis

Cell Death

Irreversible Cell Injury

A sequence of morphologic changes

that follow cell death in living tissue

A distinctive and important mode

of cell death regulated by genes

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Necrosis

Two essentially concurrent processes to

produce the morphologic changes :

1. Enzymatic digestion of the cell

2. Denaturation of proteins

(1)

Autolysis

Heterolysis

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Necrosis

Basic pathologic changes

Types of necrosis

Sequences of necrosis

(2)

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Necrosis

Basic Pathologic Changes

(3)

◆ Nuclear changes

Karyolysis

Pyknosis

Karyorrhexis

◆ Cytoplasm Increased eosinophilia

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Necrosis

Types of Necrosis

(4)

◆ Liquefactive necrosis

◆ Fat necrosis

◆ Coagulative necrosis

◆ Caseous necrosis

◆ Gangrene

◆ Fibrinoid necrosis

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Coagulative Necrosis

◆ A mass of coagulated, pink-staining,

homogeneous cytoplasm

◆ Preservation of the basic structure

outline of the coagulated cell or

tissue for several days

◆ In solid organs (kidney, heart, spleen )

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Liquefactive Necrosis

◆ Liquefaction of necrotic cells

◆ Condition: Presence of more

abundant proteolytic enzymes

◆ Most often in suppurative

inflammation & in the brain

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A small abscess in the liver.

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Liquefactive necrosis of the brain

(Encephalomalacia)

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Caseous Necrosis

◆ A distinctive form of coagulative

necrosis

◆ Cheese-like

◆ An amorphous coarsely granular

eosinophilic debris

◆ Most often in foci of TB

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A tuberculous lung with a large area of caseous

necrosis. The caseous debris is yellow-white and

cheesy.

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Fat Necrosis

◆ A special type of liquefactive necrosis

◆ Focal areas of fat destruction

◆ Calcium soaps

◆ Enzymatic fat necrosis(acute pancreatitis)

◆ Nonenzymatic fat necrosis (following

direct trauma to adipose tissue &

extracellular liberation of fat)

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Foci of fat necrosis with saponification in the mesentery.

The areas of white chalky deposits represent calcium

soap formation at sites of lipid [email protected]

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This is fat necrosis of the pancreas. Cellular injury to the pancreatic acini

leads to release of powerful enzymes which damage fat by the production

of soaps, and these appear grossly as the soft, chalky white areas seen

here on the cut surfaces.

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Microscopically, fat necrosis is seen here. Though the

cellular outlines vaguely remain, the fat cells have lost

their peripheral nuclei and their cytoplasm has become a

pink amorphous mass of necrotic material.

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Gangrene

◆ Extensive tissue necrosis

◆ Secondary bacterial infection

⚫ Dry gangrene

⚫ Wet gangrene

⚫ Gas gangrene

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This is gangrene, or necrosis of many tissues in a body

part. In this case, the toes were involved in a frostbite

injury. This is an example of "dry" gangrene in which there

is mainly coagulative necrosis from the anoxic injury.

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Toxic megacolon. Complete cessation of colon

neuromuscular activity has led to massive dilatation of

the colon and black-green discoloration signifying

gangrene and impending rupture.

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The small intestine is infarcted. The dark red to grey infarcted bowel

contrasts with the pale pink normal bowel at the bottom. Some organs such

as bowel with anastomosing blood supplies, or liver with a dual blood suppy,

are hard to infarct. This bowel was caught in a hernia and the mesenteric

blood supply was constricted by the small opening to the hernia sac.

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Fibrinoid Necrosis

◆ A type of connective tissue necrosis

◆ Loss of normal structure

◆ A homogeneous,bright pink-staining

necrotic material that resembles

fibrin microscopically

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恶性高血压病的肾脏小动脉

Sometimes the small arteries and arterioles can be damaged so severely in

malignant hypertension that they demonstrate necrosis with a pink fibrin-like

quality that gives this process its name--fibrinoid necrosis. [email protected]

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Necrosis

Sequences of Necrosis

(5)

◆ Dissolution & absorption

◆ Organization & encapsulation

◆ Autolysis & inflammation

◆ Sloughing

◆ Calcification

Ulcer, Cavity, Sinus, Fistula

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Apoptosis

◆ A distinctive & important mode of

cell death

◆ Differentiation from necrosis

◆ Morphologic appearance

of programmed cell death

◆ Important physiologic &

pathologic processes

Greek, “falling leaves”

(1)

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Apoptosis

◆ Cell Shrinkage

◆ Chromatin Condensation

◆ Apoptotic Bodies Formation

◆ Phagocytosis of Apoptotic Bodies

by Neighbouring Cells or Macrophages

Morphological Evidence

(2)

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A, Apoptosis of epidermal cells in an immune-mediated reaction. The

apoptotic cells are visible in the epidermis with intensely eosinophilic

cytoplasm and small, dense nuclei. H&E stain. (Courtesy of Dr. Scott

Granter, Brigham and Women's Hospital, Boston, MA.) B, High power of

apoptotic cell in liver in immune-mediated hepatic cell injury.

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The sequential ultrastructural changes seen in

necrosis (left) and apoptosis (right).

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Apoptosis

◆ Signaling

◆ Control & integration

◆ Execution

◆ Removal of dead cells

Mechanisms of Apoptosis

(3)

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SECTION 3

CAUSES & MECHANISMS OF CELL

INJURY

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Causes of Cell Injury◆ Hypoxia

◆ Chemical Agents

◆ Physical Agents

◆ Infectious Agents

◆ Immunologic Reactions

◆ Genetic Defects

◆ Nutritional Imbalances

◆ Aging

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Mechanisms of Cell Injury

◆General Biochemical Mechanisms

◆ Ischemic & Hypoxia Injury

◆ Ischemia / Reperfusion Injury

◆Free Radical-Induced Cell Injury

◆Chemical Injury

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