Gross pathology Flashcards

1
Q

What criteria should be used to describe lesions

A

Location
Number/extent
Demarcation
Distribution
Colour
Size
Shape
Consistency & texture

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2
Q

Name these types of distribution

A
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3
Q

Name these shapes/demarcations

A
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4
Q

What do the different colours in pathology mean

A
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5
Q

What are some possible consistencies and textures?

A
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6
Q

Describe this lesion

A

On (1.) forelimb, clipped area measuring 10 x 5 cm. Within clipped area is (2.) 1 (3.) well-demarcated, (4.) focal, (5.) pink to dark red, (6.) 3cm in diameter x 2cm height (7.) round, raised, (8.) firm, hairless mass

(Probably a mast cell tumour)

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7
Q

Describe this lesion in a dog

A

(1.) stomach was (4.) diffusely distended, (8). gas-filled & (5.) diffusely dark red

(Stomach: Necrosis, diffuse, severe, acute with dilation. Gastric torsion?)

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8
Q

Describe this lesion in a dog

A

Affecting (2.) 20% of (1.) right kidney, within renal cortex & extending into medulla, was a (4.) focal, (3.) well-demarcated, (6.) 3 x 2cm, (5.) light tan to dark red, (7.) wedge-shaped lesion

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9
Q

Describe this lesion in a cat

A

Affecting (2.) 30% of tongue, (1.) on left underside & extending to lingual surface, there was (4.) a focal, (3.) moderately well demarcated, (5.) pink to red, (6.) 5 x 2 x 1cm, (7.) oval, (8.) multinodular, firm mass

(tongue: probably squamous cell carcinoma)

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10
Q

Describe this lesion in a horse

A

(4.) Focally extensively, (1.) effacing perineum & base of tail, was (2.) a (3.) well-demarcated, (5.) black to red, (6.) approx 1m by 50cm x 10cm, (8.) ulcerated, multinodular mass

(probably a melanoma)

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11
Q

Describe this lesion in a chicken

A

Adhered to viscera & mesentery of ileum & paired caeca, were numerous, well demarcated, multifocal, up to 2cm in diameter, pink to tan, round firm masses

(Ileum, caeca: probably adenocarcinoma arising from ovary, oviduct or pancreas as these common in ageing hens)

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12
Q

describe this lesion in a cow

A

Affecting up to 90% of mammary gland, there was multifocal to coalescing, poorly demarcated areas of grey to light pink, friable tissue, admixed with haemorrhage & abundant light pink purulent exudate (pus)

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13
Q

What are the possible causes of cell injury?

A

Oxygen deprivation
Physical agents
Chemical agents and drugs
Infectious agents
Immunologic reactions
Genetic derangements
Nutritional imbalances

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14
Q

What are some possible causes of hypoxia (oxygen deficiency)?

A

Reduced blood flow (ischaemia)

Inadequate oxygenation of blood (cardiorespiratory failure)

Decreased oxygen-carrying capacity of blood (anaemia, carbon monoxide poisoning, blood loss)

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15
Q

Give examples of physical agents that can cause cell injury

A

Mechanical trauma

Extremes of temperature

Radiation

Electric shock

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16
Q

Give examples of chemical agents & drugs that can cause cell injury

A

Hypertonic concentrations (glucose, salt)

Poisons (arsenic, cyanide)

Environmental pollutants

Insecticides, herbicides

Therapeutic drugs

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17
Q

Give examples of infectious agents that can cause cell injury

A

Viruses (and prions)

Bacteria

Fungi

Protozoa

Helminths

Other (eg ecto-)parasites

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18
Q

Give examples of immunologic reactions that can cause cell injury

A

Immune reactions to external agents (microbes) & environmental substances

Immune reactions to endogenous self-antigens (autoimmune diseases)

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19
Q

What is reversible degeneration?

A

Early response to cell injury

Depletion of cellular energy stores (ATP):
- cellular swelling/fatty change
- alteration of intracellular organelles
- affects functionality of cell

reversible if damaging stimulus is removed

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20
Q

Why do cells swell after injury?

A
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21
Q

What causes fatty changes after cell injury?

A
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22
Q

What are some irreversible cell injuries?

A

Necrosis & apoptosis

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23
Q

describe necrosis after cell injury

A

Always pathologic

Cell membranes damaged

Often with inflammation (neutrophils attack leaked cell content)

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24
Q

Describe apoptosis after cell injury

A

May be physiologic or pathologic

Cell membranes intact

No inflammation

Cell suicide/programmed death

Cell shrinks

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25
Q

What are the microscopic morphologic alterations that occur in necrosis?

A
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26
Q

Label the histological signs of necrosis

A
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27
Q

Give examples of the patterns of tissue necrosis (macroscopic morphologic alterations)

A

Coagulative necrosis
Liquefactive necrosis
Gangrenous necrosis
Caseous necrosis
Fat necrosis

28
Q

Describe coagulative necrosis

A

Localised area of coagulative necrosis caused by ischaemia due to vascular obstruction

29
Q

Describe liquefactive necrosis

A

Collection of necrotic neutrophils & tissue debris (pus)

(abscess = encapsulated pus)

30
Q

Describe gangrenous necrosis

A

Variant of coagulative necrosis

Usually applied to a limb that has lost its blood supply (also tail, ears, udder)

3 types of gangrene: dry, moist or gas

31
Q

Describe caseous necrosis

A

Conversion of dead cells into friable mass resembling cheese

Typically more chronic than coagulation necrosis

e.g. Tuberculosis, Pseudotuberculosis

32
Q

Describe fat necrosis

A

Focal areas of fat destruction

Fat appears white, firm & chalky

Typically resulting from release of pancreatic lipases

33
Q

What are the microscopic morphologic alterations seen after apoptosis?

A

Cell shrinkage

Chromatin condensation

Cytoplasmic blebs & apoptotic bodies

Phagocytosis of apoptotic cells or cell bodies

34
Q

What are cell/tissue adaptations?

A

Reversible functional & structural responses to more severe physiological stresses & some pathologic stimuli , allowing cell to survive & continue to function

Changes in size, number, phenotype, metabolic activity or function of cells

Cell injury once limits of adaptive responses are exceeded

35
Q

What are the types of tissue adaptations & their causes?

A
36
Q

Describe the ability of labile cells to adapt

A

Routinely proliferate

e.g. epidermis, intestinal epithelium, bone marrow cells

37
Q

Describe the ability of stable cells to adapt

A

Intermediate in ability of regenerate/divide

e.g. bone, cartilage, smooth muscle

38
Q

Describe the ability of permanent cells to adapt

A

Very little capacity to regenerate

e.g. neurons, cardiac/skeletal muscle cells

39
Q

In what cell types can hypertrophy occur

A

most organs/tissues

Mainly in stable or permanent cells

40
Q

In what cell types can hyperplasia occur

A

Only in organs with dividing cells

Mainly labile cells

41
Q

describe hypertrophy & its stimuli

A

Increase in size of cells (by producing more organelles) resulting in increase in size of organ

Stimuli:
- increased functional demand (e.g. muscle)
- Stimulation by hormones (e.g. uterus during pregnancy)
- growth factors or viruses

Not always useful as blood supply may not increase adequately to serve increased mass

(Hypertrophy & hyperplasia often occur together & have same gross appearance)

42
Q

describe hyperplasia & its stimuli

A

Increase in number of cells in organ/tissue, resulting in increased mass/size

Stimuli:
- increased functional demand (e.g. muscle)
- Stimulation by hormones (e.g. uterus during pregnancy)
- growth factors or viruses

(Hypertrophy & hyperplasia often occur together & have same gross appearance)

43
Q

What is atrophy

A

decrease in cell size & number, resulting in reduced size of organ/tissue

44
Q

Give examples of physiologic atrophy

A

e.g. during embryonal/fetal development, uterus atrophy after parturition

45
Q

Give examples of pathologic atrophy

A

Decreased workload (atrophy of disuse)

Loss of innervation (denervation atrophy)

Diminished blood supply

Inadequate nutrition

Loss of endocrine stimulation

Pressure

46
Q

describe metaplasia & its causes

A

Potentially reversible change in which a differentiated cell type (epithelial or mesenchymal) is replaced by another cell type

Most common: columnar to squamous epithelial

Causes:
- chronic irritation
- deficiencies (e.g. Vit A)
- result of cell/tissue injury
- oestrogen toxicity

47
Q

What are the types of disorders of growth & their definitions

A

Agenesis: never developed

Aplasia: started development but stopped early

Atresia: absence of an orifice

Hypoplasia: incomplete development

Dysplasia: disordered growth

Neoplasia: abnormal growth of cells

48
Q
A

Small intestine: enteritis, necrohaemorrhagic, segmental, acute, severe

Aetiology: Parvovirus infection

49
Q
A

No, this is livor mortis

50
Q
A

hemangiosarcoma

51
Q
A

Haired skin of face & neck is multifocally elevated by well-demarcated, round, red, hairless, firm, nodular masses that measure approx 5-10mm in diameter

52
Q
A

Heart, left ventricle: Myocardial hypertrophy, diffuse, severe, chronic

53
Q
A

Lungs & thoracic cavity: haemorrhage, multifocal to coalescing, severe, acute with moderate haemothorax

(In this case haemorrhage was due to ingestion of anticoagulant rodenticides)

54
Q
A

Conjunctiva: Mucopurulent exudative conjunctivitis, marked, regional, acute to subacute with regional, moderate, oedema

55
Q
A

Cerebrum: Meningioma

56
Q
A

No, its not a lesion

This is pseudomelanosis

57
Q
A

Mandibular oral mucosa: Oral malignant melanoma

Very aggressive

Neoplasm is invading into bony structures of mandible

58
Q
A

Not a lesion

Body as a whole: oedema, diffuse, severe (consistent with anasarca)

possible causes:
- decreased intravascular oncotic pressure
- increased venous hydrostatic pressure

59
Q
A

Long bone: physeal fracture, focally extensive, severe, acute

60
Q
A

haired skin over dorsal scapula: important differential in this location is feline injection site sarcoma

These neoplasms can be very aggressive

61
Q
A

Urinary bladder: urolithiasis & chronic, diffuse, moderate, cystitis

62
Q
A

Diaphragm: herniation of abdominal viscera, focal, severe, acute with compression of pulmonary parenchyma

63
Q
A

Within duodenum is focal, full thickness, perforation with 1.5cm diameter

64
Q
A

Haired skin, chin: folliculitis, multifocal, moderate, chronic

65
Q
A

Thyroid glands: adenomatous hyperplasia, multifocal & bilateral, severe, chronic

66
Q
A

Perianal gland: adenoma