Introduction to Pathology, Cellular adaptation, Inflammation Flashcards

1
Q

“Pathos” means

A

suffering

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2
Q

“logos” means

A

study of

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3
Q

The study of disease, the origin of disease, and its development.

A

Pathology

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4
Q

Investigates the cause of disease by studying the associated changes in the cells, tissues, and organs (gives rise to the signs and symptoms of the disease).

A

Pathology

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5
Q

The origin of the disease e (underlying causes and modifying factors).

A

Etiology

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6
Q

Steps in the development of the disease.

A

Pathogenesis

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7
Q

Refers to why a disease arises.

A

Etiology

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8
Q

Describes how a disease develops.

A

Pathogenesis

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9
Q

[2] Primary Divisions of Pathology (traditional)

A
  1. General pathology
  2. Systemic pathology
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10
Q

Focuses on the cellular and tissue alterations caused by pathologic stimuli in most tissues.

[traditional]

A

General pathology

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11
Q

broad

[traditional]

A

General pathology

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12
Q

Examines the reactions and abnormalities of different specialized organs.

[traditional]

A

Systemic pathology

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13
Q

per organ system

[traditional]

A

Systemic pathology

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14
Q

[2] Primary Divisions of Pathology (modern)

A
  1. Anatomic pathology
  2. Clinical pathology
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15
Q

aka “surgical pathology”

[modern]

A

Anatomy pathology

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16
Q

Focuses of the examination of organs, tissues, and body fluids for structural abnormalities including autopsy examination of cadavers.

[modern]

A

Anatomy pathology

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17
Q

aka “laboratory medicine”

[modern]

A

Clinical pathology

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18
Q

Focuses on the examination of blood and other body samples for functional abnormalities.

[modern]

A

Clinical pathology

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19
Q

A medical doctor who examines bodies and body tissues. He or she is also responsible for performing lab tests.

A

Pathologist

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20
Q

Involved in establishing the diagnosis of the disease.

A

Pathologist

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21
Q

[4] Principal adaptive responses.

A
  1. Hypertrophy
  2. Hyperplasia
  3. Atrophy
  4. Metaplasia
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22
Q

Adaptive capability is exceeded or if the external stress is inherently harmful.

A

Cell injury

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23
Q

One of the most crucial events in the evolution of disease in any tissue or organ.

A

Cell death

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24
Q

lack of blood flow.

A

ischemia

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25
Q

[3] Cellular adaptations to stress.

A
  1. Retrogressive changes
  2. Progressive changes
  3. Degenerative changes
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26
Q

organ/tissues smaller than normal.

[cellular adaptations to stress]

A

Retrogressive changes

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27
Q

organ/tissues larger than normal.

[cellular adaptations to stress]

A

Progressive changes

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28
Q

Tissue have abnormalities.

[cellular adaptations to stress]

A

Degenerative changes

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29
Q

[3] Hypertrophy in Progressive changes.

(TFC)

A
  1. True hypertrophy
  2. False hypertrophy
  3. Compensatory hypertrophy
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30
Q

Usually seen in skeletal muscle, heart, kidneys, endocrine glands due to increased work load.

[hypertrophy in progressive changes]

A

True hypertrophy

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31
Q

Due to edema fluid and connective tissue proliferation.

[hypertrophy in progressive changes]

A

False hypertrophy

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32
Q

Involves one of paired organs when the opposite organ has been removed.

[hypertrophy in progressive changes]

A

Compensatory hypertrophy

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33
Q

[2] Hyperplasia in Progressive Changes

(PP)

A
  1. Physiological hyperplasia
  2. Pathologic hyperplasia
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34
Q

Resulting from normal stimuli, hormonal such as hyperplasia of breast and uterus during pregnancy.

[hyperplasia in progressive changes]

A

Physiological hyperplasia

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35
Q

Stimulation of growth factors, excess hormonal stimulation, viral infection, nodular.

[hyperplasia in progressive changes]

A

Pathologic hyperplasia

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36
Q

Refers to an increase in size of tissues or organs due to increase in size. NO NEW CELLS

A

Hypertrophy

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37
Q

Refers to an increase in size of an organ or tissue due to increase in the number of cells. CELL DIVISION

A

Hyperplasia

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38
Q

Reversible change involving transformation in one type of adult cell to another.

A

Metaplasia

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39
Q

[4] Degenerative changes - due to aberrations of cellular growth patterns.

(MDAN)

A

Metaplasia
Dysplasia
Anaplasia
Neoplasia

40
Q

Regressive alteration in adult cells manifested by variation in size, shape, and orientation. Usually reversible and do not lead to tumor formation - CHANGES IN STRUCTURE

(atypical hyperplasia)

41
Q

Usually used as criterion toward malignancy - irreversible, more primitive cells.

(undifferentiated cell)

42
Q

Continuous abnormal proliferation of the cells without control (no purpose or function).

(tumor)

43
Q

“NEO” in neoplasia means?

44
Q

Pathologic over growth of the tissue.

45
Q

The study of cancer.

46
Q

[2] Characteristics of tumor:

(PS)

A
  1. Parenchyma
  2. Stroma
47
Q

active elements, tumor cells, tumor itself.

[characteristics of tumor]

A

Parenchyma

48
Q

connective tissue, framework.

[characteristics of tumor]

49
Q

[2] Nomenclature of neoplastic cells.

(BM) (tumors)

A

Benign tumors
Malignant tumors

50
Q

Are those that do not produce death. Tumor is localized and doesn’t metastasize.

[tumors]

A

Benign tumors

51
Q

Will produce death eventually, however small they may be and wherever they may be located. Invasive and destroys adjacent areas.

[tumors]

A

Malignant tumors

52
Q

mesenchymal/connective tissue.

[suffix]

53
Q

epithelial tissue.

[suffix]

54
Q

Most reliable feature of malignancy.

A

Metastasis

55
Q

Tumour implants continuous with the primary tumour.

A

Metastasis

56
Q

Cancer cells penetrate into blood vessels, lymphatic’s and body cavities providing opportunity to spread.

A

Metastasis

57
Q

All neoplasm metastasize EXCEPT

A

Glial cells
Basal cell carcinoma

58
Q

[3] Manner of Dissemination of Malignant Neoplasms.

A
  1. Seeding within body cavities
  2. Lymphatic spread
  3. Hematogenous spread
59
Q

Neoplasm penetrates into a ‘’natural field’’. Most often in the peritoneal cavity.

[Manner of Dissemination of Malignant Neoplasms.]

A

Seeding within body cavities

60
Q

Most common pathway for CARCINOMAS (Epithelial)

[Manner of Dissemination of Malignant Neoplasms.]

A

Lymphatic spread

61
Q

Most common pathway for SARCOMAS (connective tissue)

[Manner of Dissemination of Malignant Neoplasms.]

A

Hematogenous spread

62
Q

Resembling normal cells

[un/differentiated cells]

A

Differentiated cells

63
Q

Younger form.

[un/differentiated cells]

A

Undifferentiated cells

64
Q

It is based on the size of the primary lesion, its extent of spread to regional lymph nodes and the presence or absence of metastases.

65
Q

2 major agencies concerned with the staging of malignant disease are:

A
  1. UICC - International Union against Cancer
  2. AJCS - American Joint Committee on Cancer staging
66
Q

Applicable to all form of neoplasia.

A

TNM system of cancer staging

67
Q

A score is based upon the size of invasion.

[letter]

68
Q

With increasing size of the primary lesion.

[letter]

A

T1, T2, T3, T4

69
Q

A score indicates the extent of lymph node involvement.

[letter]

70
Q

Indicates progressively advancing nodal disease.

[letters]

A

N0, N1, N2, N3

71
Q

A score indicates whether distant metastasis are present.

[letter]

72
Q

Whether there are distant metastases.

[letters]

73
Q

Type of neoplasm and a compound tumors.

74
Q

Greek: “MONSTROUS TUMORS”

75
Q

Tumor with normal tissue or organ components that are inappropriate to surrounding tissues.

76
Q

[2] Retrogressive changes.

A
  1. Developmental defects
  2. Atrophy
77
Q

[4] Developmental changes

[AAHA]

A
  1. Aplasia
  2. Agenesia
  3. Hypoplasia
  4. Atresia
78
Q

Incomplete/defective development of tissue/organ.

[developmental changes - retrogressive]

79
Q

Most commonly seen in one paired structures (kidneys, gonads, adrenals).

[developmental changes - retrogressive]

80
Q

Non-appearance of an organ.

[developmental changes - retrogressive]

81
Q

Failure of an organ to reach its full, mature size.

[developmental changes - retrogressive]

A

Hypoplasia

82
Q

Failure of an organ to form an opening.

[developmental changes - retrogressive]

83
Q

Refers to an acquired decrease in the size of a normally tissue or organ. REDUCTION IN CELL SIZE.

[retrogressive changes]

84
Q

[2] Atrophy

A
  1. Physiologic
  2. Pathologic
85
Q

Due to decreased work load.

A

Physiologic

86
Q

Due to denervation of muscle, diminished blood supply.

[atrophy]

A

Pathologic

87
Q

Who developed TNM system?

88
Q

Occurs as a natural consequence of maturation, as in atrophy of the thymus and lymphoid tissue during puberty. Sexual organs and brain begin to atrophy at age 50.

[types of atrophy]

A

Physiologic atrophy

89
Q

Refers to a decrease in size of organ, usually as a consequence of disease.

[types of atrophy]

A

Pathologic atrophy

90
Q

[1] Physiologic atrophy

A

Senile atrophy

91
Q

[6] Pathologic atrophy’ retrogressive changes

[VPS, AEE]

A

1.Vascular atrophy
2. Pressure atrophy
3. Starvation or hunger atrophy
4. Atrophy of disuse
5. Exhaustion atrophy
6. Endocrine atrophy

92
Q

(due to lack of nutrition) occurs if the blood supply to an organ or tissue becomes reduced below critical level.

[pathologic atrophy]

A

Vascular atrophy

93
Q

Persistent pressure on the organ or tissue may directly injure the cells or may secondarily promote diminution of blood supply.

[pathologic atrophy]

A

Pressure atrophy

94
Q

Due to excessive lack of nutritional supply, may lead to wasting of tissues.

[pathologic atrophy]

A

Starvation or hunger atrophy

95
Q

Inactivity or diminished function of a tissue or organ may lead to narrowing of blood vessels, with loss of nutrition atrophy occur;

[pathologic atrophy]

A

Atrophy of disuse

96
Q

Prolonged overwork, especially of an endocrine organ may produce initial enlargement with ultimate slow progressive loss of parenchymal cells.

[pathologic atrophy]

A

Exhaustion atrophy

97
Q

Diminished or absent endocrine stimulation may produce functional atrophy.

A

Endocrine atrophy