L14 Flashcards

1
Q

What do we mean by Neoplasia ? And what is it

A

new growth and it is uncontrolled cell division non responsive to growth controls
- Pathologic, Progressive, Purposeless,
Endless, Proliferation of cells characterized by
loss of control over cell division

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2
Q

What is the definition of neoplasm ?

A

is an 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 the cessation
of the stimuli which evoked the change.

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3
Q

‏?What is the origin of all neoplasms

A

‏The origin of all neoplasms is genetic changes that allow excessive and unregulated proliferation

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4
Q

‏ ?How do neoplasms proliferate

A

‏The proliferation is independent of physiologic growth-regulatory stimuli

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5
Q

How do neoplastic cells grow?

A

‏Neoplastic cells grow autonomously and steadily increase in size regardless of their local environment and the nutritional status of the host

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6
Q

‏?Do neoplasms depend on the host

A

‏Yes, all neoplasms depend on the host for their nutrition and blood supply

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7
Q

‏?What is the origin of neoplasms

A

‏Neoplasms are of monoclonal origin: the parenchymal cells in a neoplasm, whether benign or malignant, resemble each other, as though all had been derived from a single progenitor

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8
Q

‏?Are genetic alterations in cancer cells passed on

A

‏Yes, genetic alterations in cancer cells are heritable, being passed to daughter cells upon cell division

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9
Q

‏What are mutations and epigenetic alterations in cancer cells ?

A

‏Mutations and epigenetic alterations convey to cancer cells are referred to as cancer hallmarks

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10
Q

What do you know about CANCER ?

A

 Common term for all malignant tumors
 Crab
 Malignant tumor

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11
Q

Histogenesis of Tumors?

A

Epithelial tissues: Stratified squamous Glands or ducts Respiratory passagesNeuroectodermRenal epitheliumLiver cells Urinary tractPlacental (trophoblast) Germ cells

Mesenchymal tissues: Connective tissue and derivatives Endothelial and related tissues Blood cells and related tissues Lymphoid tissue Muscle – smooth or striated Bone, cartilage & synovium

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12
Q

‏What is a characteristic of benign tumors regarding their ability to spread?

A

‏ tumors remain localized and cannot spread

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13
Q

How are benign tumors treated?

A

Benign tumors are treated by local surgical excision

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14
Q

‏What is the growth rate of benign tumors?

A

‏Benign tumors grow slowly

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15
Q

‏Do benign tumors have a capsule ?

A

Yes, usually Capsulated capsule result from compression of tumor, to surrounding cells, it consists of extracellular matrix that is deposited by stromal cells due to hypoxic damage to parenchymal cells.

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16
Q

‏How are the cells of benign tumors differentiated?

A

They Histologically composed of well differentiated cells ie resemble tissue of origin (The differentiation of parenchymal cells refers to the extent to which tumor resemble the tissue of origin morphologically and functionally)

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17
Q

‏What is the survival outlook for patients with benign tumors?

A

‏patient generally survives when diagnosed with a benign tumor

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18
Q

Can benign tumors produce significant morbidity or be lethal?

A

Benign tumors produce localized lumps, sometimes they produce significant morbidity or are even lethal.

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19
Q

?‏ malignant tumors usually encapsulate

A

No, malignant tumors are usually not encapsulated

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20
Q

How do malignant tumors grow?

A

They grow by progressive infiltration (invasion), destruction, and penetration of the surrounding tissue.

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21
Q

‏?Are malignant tumors associated with necrosis

A

‏Yes, malignant tumors grow quickly and are often associated with necrosis

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22
Q

‏?Do malignant tumors metastasize

A

‏Yes, malignant tumors spread to distant sites (metastasize)

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23
Q

‏What is the prognosis for malignant tumors?

A

‏The prognosis ranges from good to poor, depending on various factors.

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24
Q

‏Can malignant tumors cause death? If so, how

A

‏Yes, malignant tumors can invade and destroy adjacent structures and spread to distant sites, leading to death.

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25
Q

What are the cytologic features of malignant neoplasms?

A

‏The cytologic features of malignant neoplasms include increased nuclear size (with increased nuclear/cytoplasmic ratio - N/C ratio),
variation in nuclear or cell size (pleomorphism), lack of differentiation (anaplasia),
increased nuclear DNA content with subsequent dark staining on H&E slides (hyperchromatism), prominent nucleoli or irregular chromatin distribution within nuclei,
and increased mitoses and abnormal mitoses (especially irregular or bizarre mitoses).

26
Q

What does increased nuclear size and nuclear/cytoplasmic ratio (N/C ratio) indicate in malignant tumors?

A

‏Increased nuclear size, along with an increased nuclear/cytoplasmic ratio (N/C ratio), is a characteristic feature of malignant tumors

27
Q

What is pleomorphism in the context of malignant neoplasms?

A

‏Pleomorphism refers to the variation in nuclear or cell size, which is commonly observed in malignant neoplasms.

28
Q

How can malignant neoplasms vary in terms of differentiation?

A

‏Malignant neoplasms can range from well-differentiated (resembling normal tissue) to completely undifferentiated (anaplastic).

29
Q

What does lack of differentiation (anaplasia) signify in a tumor?

A

‏ Lack of differentiation, or anaplasia, refers to a state where the tumor cells lose the characteristics of normal cells and show abnormal features

30
Q

What is hyperchromatism, and how is it related to malignant tumors?

A

‏Hyperchromatism is an increased nuclear DNA content, which results in dark staining on H&E (Hematoxylin and Eosin) slides, a feature commonly seen in malignant tumors

31
Q

What role do nucleoli play in identifying malignant tumors?

A

‏Prominent nucleoli are often seen in malignant tumors, which may also show irregular chromatin distribution within the nuclei

32
Q

What is the significance of increased mitoses in malignant tumors?

A

‏ An increase in mitoses, particularly abnormal or bizarre mitoses, is a key feature of malignant neoplasms and indicates uncontrolled cell division

33
Q

What is the Different between Benign and Malignant tumors?

A

Benign tumour: Well circumscribed,
⦿ Usually small in size,
⦿ Slow growing,
⦿ Capsulated,
⦿ Non-invasive,
⦿ No hge. and necrosis,
⦿ Do not metastasize,
⦿ Well differentiated,
⦿ Suffix “oma” eg. Fibroma

Malignant:
⦿ Poorly circumscribed,
⦿ Usually larger in size,
⦿ Fast growing,
⦿ Not capsulated,
⦿ Invasive & infiltrative,
⦿ Hge and necrosis,
⦿ Metastasize,
⦿ Poorly differentiated,
⦿ Suffix “carcinoma” or “sarcoma”

34
Q

‏What are the two basic components of all tumors, both benign and malignant?

A

All tumors, whether benign or malignant, have two basic components:
1. Parenchyma: Made up of transformed or neoplastic cells.
2. Stroma: The supporting, host-derived, non-neoplastic component made up of connective tissue, blood vessels, and host-derived inflammatory cells.

35
Q

‏What is the parenchyma of a tumor made up of?

A

‏The parenchyma of a tumor is made up of transformed or neoplastic cells

36
Q

‏What is the stroma of a tumor made up of?

A

‏The stroma of a tumor is made up of connective tissue, blood vessels, and host-derived inflammatory cells

37
Q

‏Why is the stroma important for tumor growth?

A

‏The stroma is crucial for tumor growth because it provides the blood supply and supports the growth of parenchymal cells.

38
Q

‏What is the general principle for naming benign tumors?

A

‏Benign tumors are generally named by adding the suffix “-oma” to the cell type from which the tumor arises.

39
Q

‏How are benign tumors arising in mesenchymal tissue named?

A

‏Benign tumors arising in mesenchymal tissue are named as follows:
‏ • A benign tumor arising in fibrous tissue is called a fibroma.
‏ • A benign cartilaginous tumor is called a chondroma.

40
Q

‏How are benign epithelial tumors named based on their macroscopic pattern?

A

‏Benign epithelial tumors are named based on their macroscopic pattern as follows:
‏ • Papillomas are benign epithelial neoplasms that grow on any surface and produce microscopic or macroscopic finger-like fronds.
‏ • A polyp is a mass that projects above a mucosal surface, such as in the gut, forming a macroscopically visible structure.
‏ • Cystadenomas are tumors that form large cystic masses, such as in the ovary.

41
Q

‏How are benign epithelial tumors named based on their microscopic pattern?

A

‏Based on the microscopic pattern, the term adenoma is applied to benign epithelial neoplasms that produce glandular patterns or to neoplasms derived from glands but not necessarily exhibiting glandular patterns.

42
Q

What are malignant neoplasms arising in mesenchymal tissue or its derivatives called?

A

Malignant neoplasms arising in mesenchymal tissue or its derivatives are called sarcomas.

43
Q

What is an example of a malignant neoplasm of fibrous tissue origin?

A

A malignant neoplasm of fibrous tissue origin is called a fibrosarcoma.

44
Q

What is a malignant neoplasm composed of chondrocytes called?

A

A malignant neoplasm composed of chondrocytes is called a chondrosarcoma.

45
Q

What do we call a malignant neoplasm composed of fat-like cells?

A

A malignant neoplasm composed of fat-like cells is called a liposarcoma.

46
Q

What is the term for malignant neoplasms arising from the mesenchymal cells of the blood?

A

Malignant neoplasms arising from the mesenchymal cells of the blood are called leukemias or lymphomas.

47
Q

What are malignant neoplasms of epithelial cell origin called?

A

Malignant neoplasms of epithelial cell origin are called carcinomas.

48
Q

What are carcinomas that grow in a glandular pattern called?

A

Carcinomas that grow in a glandular pattern are called adenocarcinomas.

49
Q

What are carcinomas that arise from squamous cells called?

A

Carcinomas that arise from squamous cells are called squamous cell carcinomas.

50
Q

Can the tissue or organ of origin be identified in some malignant neoplasms?

A

Yes, in some cases, the tissue or organ of origin can be identified. For example, renal cell adenocarcinoma implies an origin from the kidneys, and cholangiocarcinoma implies an origin from the bile ducts.

51
Q

What are mixed tumors?

A

Mixed tumors are tumors (benign or malignant) in which cells undergo divergent differentiation.

52
Q

Are mixed tumors monoclonal in origin?

A

Yes, mixed tumors are of monoclonal origin, but the progenitor cell has the capacity to differentiate into more than one lineage.

53
Q

Give examples of mixed tumors?

A

• Pleomorphic adenoma: A mixed tumor of the salivary gland.
• Fibroadenoma: A mixed tumor of the female breast.
• Teratoma: A tumor originating from totipotential stem cells in the ovary and testis.

54
Q

What is the origin of teratomas?

A

Teratomas originate from totipotential stem cells, which are normally present in the ovary and testis.

55
Q

What is the differentiation capacity of totipotential stem cells in teratomas?

A

Totipotential stem cells have the capacity to differentiate into any of the cell types found in the adult body.

56
Q

What are the components of pleomorphic adenoma?

A

• Pleomorphic adenoma contains:
• Obvious epithelial components dispersed throughout a fibromyxoid stroma.
• Sometimes, it harbors islands of cartilage or bone.

57
Q

What is fibroadenoma?

A

• Fibroadenoma is a benign tumor that contains:
• A mixture of proliferated ductal elements (adenoma).
• Embedded in loose fibrous tissue (fibroma).

58
Q

What types of tissues can be found in teratomas?

A

• Teratomas are composed of:
• Bone, epithelium, muscle, fat, nerve, and other tissues.

59
Q

Where are teratomas typically found?

A

Teratomas are typically found in the ovary and testis.

60
Q

Are fibroadenomas benign or malignant?

A

Fibroadenomas are benign tumors.

61
Q

Do pleomorphic adenomas contain cartilage or bone?

A

Yes, pleomorphic adenomas sometimes contain islands of cartilage or bone.

62
Q

Can mixed tumors differentiate into more than one lineage?

A

Yes, mixed tumors can differentiate into more than one lineage due to the capacity of their progenitor cells.