disorders of growth Flashcards

1
Q

What are the two types of controlled non neoplastic disorders of growth? Briefly describe.

A

1- Congenital.
Present at birth and includes, Aplasia, Agenesis, Hypoplasia and Dysplasia
2- Acquired
Adaptive change and involves Hypertrophy, Hyperplasia, Dysplasia and Metaplasia

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2
Q

What is Metaplasia? Is it anon neoplastic of neoplastic characteristic?

A

Non neoplastic characteristic

Uncommon change which involves involves the replacement of one cell type with another. It may be reversible.

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3
Q

What is hyperplasia?. Is it anon neoplastic of neoplastic characteristic?

A

Non-neoplastic characteristic

Refers to an increase in cell number rather than cell size.

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4
Q

Define Hypoplasia and hyperplasia. Is it anon neoplastic of neoplastic characteristic?

A

Non neoplastic characteristic
Hypoplasia: Failure of an organ or tissue to achieve its full size or development
Hyperplasia: Increase in cell number

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5
Q

Define Aplasia. Is it anon neoplastic of neoplastic characteristic?

A

Non neoplastic characteristic

Complete failure of development. Agenesis is the same but you can not see a rudimentary remain

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6
Q

Define Atrophy? Is it anon neoplastic of neoplastic characteristic?

A

Non- neo

Decrease in organ/cell size and number

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7
Q

Define hypertrophy, Is it anon neoplastic of neoplastic characteristic?

A

Non- neo

Increase in cell size

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8
Q

Define dysplasia. Is it anon neoplastic of neoplastic characteristic?

A

Non-neo
Proliferation and disorganisation in tissue that may be a precursor stage leading to neoplasia eg epithelial dysplasia of the skin

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9
Q

What gene groups are altered as a result of neoplasia? And what are their usual significance?

A
Proto-oncogenes and tumour supressor cells. They are normally involved in 
•Production of growth factors
•Growth factor receptors
•Signal transduction
•DNA replication
•Apoptosis
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10
Q

Differ between the behaviour and appearance of benign and malignant disorders

A

Benign growths are slow growing, dont metastasise and are well differentiated. Malignant is opposite

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11
Q

How are proto-oncogenes altered by neoplasms?

A

Proto-oncogenes are essential for controlling normal cell devision. They are mutated into oncogenes which constantly signal cells to divide.

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12
Q

Define anaplasia. Is is a non neo or neo characteristic?

A

Neo

Loss of differentiation of cells

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13
Q

How do malignant neoplasms invade?

A

Many tumour cells produce proteolytic enzymes or induce neighbours to produce these so that they can dissolve proteins and move through tissues easier
There is also the selection for more malignant forms

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14
Q

What is the mechanism/multi step process of metastasis?

A

They travel via body cavities, lymphatics or through blood.
1. Cells must separate from each other (loss of cadherin function)
2. Cells must attach to ECM components and increase in integrin expression
3. Secrete proteases or induce cells around them to secrete proteases→enzyme that breaks down proteins
4. Migration requires coordinated cytoskeletal alterations. Stimulated by autocrine growth factors and cleavage products of ECM
5. Tumour embolisation. Cells need to break away from each other
6. Site of extravasation determined by
o vascular anatomy
o tumour surface adhesion molecules

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15
Q

What is a carcinogen and what are the 4 stages?

A
A carcinogen is a physical or chemical cancer causing agent. The 4 stages are as follows:
1- Initiation
2. Promotion
3. Progression (benign stage)
4. Malignant conversion
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16
Q

What is the major tumour suppresser gene?

A

p53

17
Q

List the 3 factors influencing congenital disorders.

A

Stage of pregnancy, Genotype of developing embryo and type of teratogen involved.

18
Q

What must infectious teratogen viruses be able to do?

A
  • Cross the placenta
  • Not kill the mother, so they need to be non pathogenic or of low pathogenicity
  • persist in specific foetal tissue
19
Q

Give examples of Infectious viral teratogens.

A
  • Akabane virus in cattle
  • Porcine parvovirus
  • Swine fever
20
Q

How does akabane virus affect a calve at different stages of gestation?

A

from 3-4 months it causeshydranencephaly
from 5-6 it causes angular limb deformities (arthrogryposis)
In the last trimester it can causes abortions or still births or neurological signs such as incoordication and paralysis if the calve survives.

21
Q

examples of nutritional deficiency teratogen

A

Iodine–>leads to goitre
Copper–>leads to enzootic ataxia
Vitamin A–>leads to ocular defects, palatine defects

22
Q

examples of toxic teratogens

A

Lupins–>leads to limb contracture in calves and lambs

Cortisone–>leads to palatine defects

23
Q

List some anatomical congenital defects

A
  • Failure to develop
  • Failure to canalis
  • Failure to close/fuse
  • ectopic location of tissue
  • Supernumeracy tissues
  • Vestigal remnants and cyts
  • Abnormal structural development