Reviewer #3 Flashcards

1
Q

a group of more than 200 diseases
characterized by uncontrolled and unregulated
growth of cells.

A

Cancer

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2
Q

Two (2) major dysfunctions in the process of cancer
development are

A

defective cell proliferation (growth)
and defective cell differentiation

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3
Q

are normal cell genes that are
important regulators of normal cell processes

A

Protooncogenes

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4
Q

Protooncogenes promote

A

cell growth.

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5
Q

Mutations that alter the expression of
protooncogenes can activate them to function as

A

oncogenes (tumor-inducing genes)

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6
Q

Tumor suppressor genes function to regulate

A

(suppress) cell growth

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7
Q

It involves a mutation in the cell’s genetic
structure.

A

Initiation

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8
Q

is characterized by the reversible
proliferation of the altered cells

A

Promotion

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9
Q

is characterized by increased growth
rate of the tumor, increased invasiveness, and
metastasis

A

Progression

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10
Q

(spread of the cancer to a distant site

A

metastasis

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11
Q

Substances considered/ suspected to be causing cancers

A

Carcinogens

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12
Q

Chemicals were identified as cancer-causing agents
in the latter part of the eighteenth century when
Percival Pott noted that

A

chimney sweeps had a
higher incidence of cancer of the scrotum

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13
Q

a multistep process beginning with the rapid
growth of the primary tumor.

A

Metastasis

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14
Q

As the tumor increases in size, development of its
own blood supply is critical to its survival and growth.
The process of the formation of blood vessels within
the tumor itself is termed tumor angiogenesis and is
facilitated by

A

tumor angiogenesis

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15
Q

involves several steps
beginning with primary tumor cells penetrating
blood vessels.

A

Hematogenous metastasis

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16
Q

In the lymphatic system, tumor cells may be
“trapped” in the first lymph node confronted or they
may bypass regional lymph nodes and travel to more
distant lymph nodes, a phenomenon termed

A

skip
metastasis.

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17
Q

The immune system has the potential to distinguish
cells that are

A

normal (self) from abnormal (nonself)
cells.

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18
Q

Cancer cells may display altered cell-surface antigens
as a result of malignant transformation. These
antigens are

A

tumor-associated antigens
(TAAS).

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19
Q

The immune system’s response to antigens of the
malignant cells 15 termed

A

immunologic
surveillance.

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20
Q

are able to directly lyse
tumor cells spontaneously without any prior
sensitization

A

Natural killer (NK) cells

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21
Q

The process by which cancer cells evade the immune
system is termed

A

immunologic escape.

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22
Q

are a type of tumor antigen.
They are found on both the surfaces and the inside
of cancer cells and fetal cells. These antigens are an
expression of the shift of cancerous cells to a more
immature metabolic pathway, an expression usually
associated with embryonic or fetal periods of life

A

Oncofetal Antigens

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23
Q

These oncofetal antigens can be used as ____ that may be clinically useful to monitor the
effect of therapy and indicate tumor recurrence.
 Tumor markers are affected by various factors that
need to be accounted for when reviewing these
results.

A

tumor
markers

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24
Q

Tumors can be classified as

A

benign or malignant

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25
Q

, benign neoplasms are

A

well differentiated

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26
Q

malignant neoplasms

A

range from well
differentiated to undifferentiated.

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27
Q

is identified by the tissue of origin, the
anatomic site, and the behavior of the tumor.

28
Q

originate from embryonal ectoderm
(skin and glands) and endoderm (mucous membrane
linings of the respiratory tract, GI tract, and
genitourinary [GU] tract

A

Carcinomas

29
Q

embryonal originate from mesoderm
(connective tissue, muscle, bone, and fat).

30
Q

leukemias originate from
hematopoietic system.

31
Q

Cells differ slightly from normal cells
(mild dysplasia) and are well differentiated (low
grade).

32
Q

Cell are more abnormal (moderate
dysplasia) and moderately differentiated
(intermediate grade).

33
Q

Cells are very abnormal (severe
dysplasia) and poorly differentiated (high grade).

34
Q

Cells are immature and primitive
(anaplasia) and undifferentiated; cell of origin is
difficult to determine (high grade).

35
Q

Grade cannot be assessed.

36
Q

Classifying the extent and spread of disease is
termed

37
Q

Stage 0

A

Cancer in situ (in place)

38
Q

Stage I

A

Tumor limited to the tissue of origin;
localized tumor growth

39
Q

Limited local spread

40
Q

Extensive local and regional spread

41
Q

Metastasis

42
Q

It is used to determine the anatomic extent of the
disease involvement according to three parameters:
tumor size and invasiveness (T), presence or absence
of regional spread to the lymph nodes (N), and
metastasis to distant organ sites (M).

A

TNM Classification System

43
Q

refers to a neoplasm whose
cells are localized and show no tendency to invade or
metastasize to other tissues.

A

Carcinoma in situ (CIS)

44
Q

refers to the extent of the disease as
determined by surgical excision, exploration, and/or
lymph node sampling.

A

Surgical staging

45
Q

It is the removal of a tissue sample analysis. for
pathologic

46
Q

Is commonly performed for
tissue that can be safely reached through the skin.

A

Percutaneous Biopsy

47
Q

May be used for lung or other
intraluminal (esophageal, bladder). lesions colon

A

Endoscopic Biopsy

48
Q

Involves the surgical removal of
the entire lesion, lymph node, nodule, or mass.

A

Excisional Biopsy

49
Q

May be performed with a
scalpel or dermal punch. The Pathologies
examines the tissue to determine whether it is
benign or malignant, the anatomic tissue from
which the tumor arises (histology), and the
degree of cell differentiation (histologic grade).

A

Incisional
Biopsy

50
Q

The goals of cancer treatment are

A

cure, control, and palliation.

51
Q

Surgical intervention can be used to
eliminate or reduce the risk of cancer development.
Prophylactic removal of nonvital organs has been
successful in reducing the incidence of some
malignancies

A

Prevention

52
Q

The objective is to remove all or as
much resectable tumor as possible while sparing
normal tissue.

A

Cure or Control

53
Q

Debulking of tumor to

A

relieve pain or pressure

54
Q

For the relief of a bowel obstruction

55
Q

for the relief of a spinal cord
compression

A

Laminectomy

56
Q

the use of chemicals as a systemic therapy for
cancer

A

Chemotherapy

57
Q

delivers the drug to the
tumor via the arteries supplying the tumor.

A

Intraarterial chemotherapy

58
Q

involves the delivery
of chemotherapy to the peritoneal cavity for
treatment of peritoneal metastases from primary
colorectal and ovarian cancers and malignant ascites

A

Intraperitoneal chemotherapy

59
Q

involves a lumbar
puncture and injection of chemotherapy into the
subarachnoid space

A

intrathecal chemotherapy

60
Q

involves
instillation of chemotherapy into the bladder

A

Intravesical chemotherapy bladder

61
Q

includes anaphylactic and
hypersensitivity reactions, extravasation or a flare
reaction, anticipatory nausea and vomiting, and
cardiac dysrhythmias.

A

Acute toxicity

62
Q

involve damage to organs such
as the heart, liver, kidneys, and lungs.

A

Chronic toxicities

63
Q

energy that is emitted from a source and
travels through space or some material.

64
Q

the most common form of radiation
treatment delivery. With this technique, the patient
is exposed to radiation from a megavoltage
treatment machine. A linear accelerator, which
generates ionizing radiation from electricity and can
have multiple energies, is the most commonly used
machine for delivering external beam radiation

A

EXTERNAL RADIATION: Teletherapy

65
Q

Radiation can also be
delivered as Brachytherapy, which means “close” or
internal radiation treatment. It consists of the
implantation or insertion of radioactive materials
directly into the tumor (interstitial) or in close
proximity to the tumor (intracavitary or
intraluminal). This allows for direct delivery of
radiation to the target with minimal exposure to
surrounding healthy tissues.

A

INTERNAL RADIATION: