Classification Of Tumors Flashcards

1
Q

abnormal mass of tissue, the growth of which
exceeds and is uncoordinated with that of the normal tissues
and persists in the same excessive manner after cessation of the
stimuli which induced the change is ?

A

neoplasm

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2
Q

Tumors are classified according to behavior into?

A

Benign tumors

– Malignant tumors

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3
Q

clue for differentiation?

A

Morphology

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4
Q

All tumors have two basic components?

A

1) The parenchyma, made up of transformed or neoplastic
cells. (2) The supporting non-neoplastic stroma, made up of
connective tissue, blood vessels, and host-derived
inflammatory cells.

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5
Q

Nomenclature?

A

Benign tumors: In general, benign tumors are designated by attaching the suffix -oma to the cell type from which the tumor arises.

Malignant tumors
• Malignant neoplasms of epithelial cells are called carcinomas
• Malignant neoplasms arising in “solid” mesenchymal tissues,
or its derivatives are called sarcomas

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6
Q

benign tumor arising in fibrous tissue is ?

A

fibroma

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7
Q

benign cartilaginous tumor is

A

chondroma

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8
Q

sarcomas,

-Exceptions

A

sarcomas, eg. Chondrosarcoma

-Exceptions

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9
Q

malformation that presents as a mass of

disorganized tissue indigenous to the particular site?

A

Hamartoma

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10
Q

mass of mature but disorganized hepatic cells,

blood vessels, and possibly bile ducts within the liver?

A

Hamartoma

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11
Q

may be a hamartomatous nodule in the lung

containing islands of cartilage, bronchi, and blood vessels ?

A

Hamartoma

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12
Q

Features to distinguish between benign and malignant neoplasm:
?

A
  1. Differentiation and anaplasia 2. Rate of growth 3. Local invasion 4. Metastasis
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13
Q

extent to which they
resemble their normal counterparts morphologically and
functionally. ?

A

1.Differentiation

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14
Q

1.Differentiation is seen in ?

A

parenchymal cells

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15
Q

Benign neoplasms 1.Differentiation?

A

well­ differentiated

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16
Q

Malignant neoplasms 1.Differentiation?

A

range of parenchymal cell
differentiation, from well differentiated to completely
undifferentiated (anaplastic) Between the two extremes lie tumors
referred to as moderately differentiated.

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17
Q

Anaplastic features?

A

Pleomorphism (variation in size and shape of cells & their
nuclei) 2. Hyperchromatic large nuclei 3. Increased nuclear ­to­ cytoplasmic ratio (1 : 1 , normal 1 : 4 ) 4. Multi nucleated Giant cells. 5. Mitoses often are numerous and distinctly atypical; tripolar or
quadripolar mitotic figures ) 6. Fail to develop recognizable patterns of orientation to one
another (i.e., they lose normal polarity).

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18
Q

2.Rate of growth:

• Most benign tumor? most malignant?

A

grow slowly, / grow

much faster.

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19
Q

Poorly differentiated tumors tend to ?

A

grow more rapidly

than do well­ differentiated tumors.

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20
Q

grow more rapidly
than do well­ differentiated tumors.
?

A

benign

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21
Q

It
does not have the capacity to infiltrate, invade, or metastasize to
distant sites.
?

A

benign

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22
Q

progressive infiltration,
invasion, destruction, and penetration of the surrounding
tissue.
?

A

Malignant

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23
Q

Means the development of secondary implants (metastases)

discontinuous with the primary tumor , ?

A

.Metastasis

24
Q

Not all cancers can metastasize ?

A
  1. Basal cell carcinomas of the skin
  2. Most primary tumors of the central nervous system, which are
    highly invasive locally but rarely metastasize.
  3. Carcinoids
  4. Giant cell tumor of bone
25
30% of patients with newly diagnosed solid tumors present with?
clinically evident metastases.
26
Malignant neoplasms disseminate by one of three path­ways?
Hematogenuos spread: 2.lympatic 3. Seeding within body cavities :
27
Hematogenuos spread: ?
Through the blood and it is favored by sarcomas
28
2.lympatic spread?
through the lymph and it is typical of | carcinomas
29
the first regional lymph node that | receives lymph flow from a primary tumor ?
sentinel lymph node”
30
sentinel lymph node” It can be identified by?
injection of blue dyes or radiolabeled tracers | near the primary tumor.
31
frequently involved secondary sites in | hematogenous dissemination. ?
Liver and lungs
32
Seeding within body cavities : | Examples ?
Characteristic of cancers of the ovary, which often cover the peritoneal sur­faces widely. • Neoplasms of the central nervous system, penetrate the cerebral ventricles and be carried by the cerebrospinal fluid to reimplant on the men­ingeal surfaces.
33
Gross Features Benign tumors | ?
Well defined tumor margins • Cut section is uniform with no hemorrhage or necrosis • Usually, small. • Tumor arising in solid organs are ovoid, capsulated from compressed surrounding structures.
34
Gross Features Malignant Tumors
Tumor margins are ill defined • Size variable. • Cut section shows hemorrhage and necrosis. • Not encapsulated usually. • Tumor arising from surface is either cauliflower , ulcerative, or infiltrative.
35
have the same structural pattern as normal tissue. ?
Benign
36
Cells of benign tumors are similar to the cell of origin. The only clue to being neoplastic is mass formation.
Benign
37
adipocytes | separated by CT) ?
Benign Lipoma
38
Thyroid adenoma | follicles
Benign
39
Cells of benign tumors are similar to the cell of origin. The only clue to being neoplastic is mass formation. Eg?
leiomyoma (fibroid) is similar to smooth muscle of the uterus.
40
MALIGNANCY FEATURES ?
• NUCLEAR SIZE (INCREASED N/C RATIO) • NUCLEAR SHAPE (PLEOMORHISM) • CHROMATIN COLOR (HYPERCHROMASIA) • CHROMATIN CLUMPS • M ITOTIC FIGURES • NUCLEOLI (M ACRONUCLEOLI OR PROMINENT NUCLEOLI
41
``` It is hard to tell the origin of tumor cells, carcinoma, sarcoma, lymphoma or melanoma. We use? ```
Immunohistochemistry
42
Plays a role in malignant tumors for identification of tumor | type, small biopsy or undifferentiated tumors. ?
Immunohistochemistry
43
Immunohistochemistry of epithelial tumors ?
Cytokeratin
44
Immunohistochemistry of mesenchymal tumors ?
Vimentin
45
Immunohistochemistry of lymphoma?
Leukocytic Common Antigen (LCA
46
Immunohistochemistry of melanoma?
Melan A,
47
For tumor therapy, targeted and hormonal – Breast carcinoma which Immunohistochemistry is used ?
``` ER • PR • HER2 • KI67 • OTHERS ```
48
Slower rate of growth • Local invasion without | distant metastasis. ?
Locally Malignant Tumors
49
loss in the uniformity of the individual cells | and a loss in their architectural orientation.
Dysplasia
50
Dysplasia occurs in ?
• It occurs mainly in the epithelia meneschymal
51
It is a non-neoplastic process but a premalignant | condition.
Dysplasia
52
Dysplasia properties?
is showing a degree of pleomorphism, incearse N:C ratio, hyperchromatism, increase mitosis, loss of polarity and disordered maturation or total failure of maturation • Dysplasia does not mean cancer. • Dysplasia does not necessary progress to cancer. • Dysplasia may be reversible. BUT Lack of invasiveness • Reversibility .
53
The differences between dysplasia and cancer: ?
Lack of invasiveness • Reversibility
54
The risk for invasive cancer varies with: ?
Grade of dysplasia ( mild, moderate, | sever) • Duration of dysplasia • Site of dysplasia
55
``` an intraepithelial malignancy in which malignant cells involve the entire thickness of the epithelium without penetration of the basement membrane. ? ```
Carcinoma In-situ