Pathophysiology (cells and inflammation) Flashcards

1
Q

What are the 2 main parts of the skin (the integument) and what are the accessory structures?

A
  1. the epidermis- superficial thinner part, composed of epithelial tissue
  2. the dermis- deeper thicker part, composed of dense irregular connective tissue

Accessory structures: hair, oil glands, sweat glands, nails, and sensory receptors

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2
Q

What are the 5 layers of the skin?

A
  1. stratum basale- deepest layer
  2. stratum spinous- provides strength and flexibility
  3. stratum granulosum- keratinocytes undergo apoptosis
  4. stratum corneum- most superficial layer
  5. stratum lucidem- only thick skin between granulosum and corneum
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3
Q

What are the 4 main types of cells in the skin?

A
  1. keratinocytes= produce protein keratin
  2. melanocytes= produce pigment melanin
  3. intraepidermal macrophages (langerhans cells)= involved in immune response
  4. tactile epithelial cells= detect touch
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4
Q

What is the healing process for an epidermal wound?

A

-basal cells at the edges of the wound become free from the basement membrane and migrate across the wound in a sheet like manner. This continues until epidermal cells meet each other (contact inhibition) and the wound is closed
-the hormone epidermal growth factor is secreted and this stimulates basal cells to divide and replace the ones that moved into the wound

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4
Q

What is a deep wound?

A

One that extends to the dermis and below, meaning skin healing has to take place in all layers

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5
Q

what are the phases of deep wound healing

A
  1. inflammation- blood clot forms, elimination of microbes, preparing for repair
  2. migration- clot becomes a scab, epithelial cells migrate to bridge the wound below the scab
  3. proliferation- extensive growth of cells below the scab
  4. maturation- scab sloughs off once epidermis returns to normal thickness
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6
Q

What are pressure ulcers and what are the 3 main causes?

A

-wounds which involve ischaemic damage (blood flow restricted) to the skin and underlying tissue

3 main causes:
-pressure (weight of body causes capillary occlusion)
-shear (layers of skin are stretched)
-friction (caused when part of body rubs against a surface)

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7
Q

What are the different pressure ulcer grades according to European Pressure Ulcer Advisory Panel

A

grade 1- non-blanching erythema of intact skin

grade 2- a lesion involving a clear blister

grade 3- a lesion involving full thickness skin loss

grade 4- a lesion in which tunnelling is present

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8
Q

What is the difference between primary wound intention, secondary wound intention and tertiary wound intention?

A

Primary intention- wound is clean with little tissue loss, and edges are brought together by stitches, staples, skin glue etc e.g surgical incision

Secondary intention- edges cannot be brought together due to extent of tissue loss. takes a long time to heal and more prone to infection

Tertiary intention- wound edges could be brought together as little tissue loss, but not done immediately due to infection or contamination. Wound closed by suturing

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9
Q

What is a superficial burn?

A

-involves only the epidermis
-mild pain and redness but absence of blisters
-functions of skin not impaired
-healing will take place over a few days

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10
Q

What is a partial thickness burn?

A

-involves damage to the epidermis and dermis
-redness, blisters, oedema and pain
-some functions of skin will be lost
-healing will take a number of weeks and may be scarring

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11
Q

What is a deep partial thickness burn?

A

-damage to the epidermis and deeper into dermis affecting structures
-slow to heal and may involve surgery

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12
Q

What is a full thickness burn?

A

-damage to both the epidermis and dermis which extends to the subcutaneous layers
-loss of most functions of the skin
-always requires reconstructive surgery e.g skin graft

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13
Q

What are the 4 different ways bone fractures can be classified?

A
  1. position of bone ends
  2. completeness of break
  3. orientation of break
  4. bone ends penetration of skin
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14
Q

What is a compound fracture?

A

-a bone fracture that is accompanied by breaks in the skin, causing the broken ends of bone to come into contact with the outside environment

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15
Q

What is a displaced fracture?

A

-pieces of bone moved so much that a gap formed around the fracture when the bone breaks

16
Q

What is a green stick fracture?

A

-a partial fracture where only the cortex and periosteum are interrupted on one side of the bone but remain uninterrupted on the other

17
Q

What is a vertical fracture?

A

-instead of a horizontal break across the bone, a linear fracture is vertical and parallel to the sides of the bone

18
Q

What is the bone fracture repair process?

A
  1. Hematoma formation (death of some bone cells, pain and swelling)
  2. fibrocartilaginous formation
    (granulation tissue fills gap and rejoins fracture)
  3. soft callus converts to bony callus
  4. bone remodelling
    (compact bone laid, osteoblastic activity occurs)
19
Q

What is a single point mutation?

A

-involves a change in a single base along the base sequence of a particular gene
-a point mutation can also be a deletion or addition, where one or more bases are deleted or added

20
Q

What are the different categories of genetic diseases and give an example of a disease of this category?

A

-autosomal dominant
e.g Huntingdon’s disease

-autosomal recessive
e.g sickle cell disease

-sex linked recessive
e.g haemophilia

21
Q

What is epigenetics?

A

-the term used to refer to factors that influence how genes are expressed within the cells in the body
-this brings about a lasting change in genetic information

22
Q

What are the 3 processes that gene activation and deactivation can occur by?

A
  1. DNA methylation- methyl group is added directly to a cytosine residue that exists in a CpG sequence
  2. Histone modification- acetyl and methyl groups are added directly onto histone tails which changes how genes are expressed
  3. RNA changes
23
Q

What are the 2 groups of proteins responsible for the progress of cells through various checkpoints of the cell cycle?

A

Cyclins and Cyclin-dependent kinases (Cdks)

24
Q

What are proto-oncogenes and what do they do? Give some examples

A

-Normal genes which affect normal cell growth and proliferation but also have the potential to contribute to cancer development if their expression is altered

-they turn the cell on to divide (car accelerator)

-growth factors, receptors, signalling enzymes, transcription factors

25
Q

What are tumour suppressor genes and what do they do? Give some examples

A

-a family of normal genes that instruct cells to produce proteins that restrain cell growth and division

-They turn cell division off- loss of these proteins allow a cell to grow in an uncontrolled fashion

-like a break pedal that doesn’t work

26
Q

What are DNA repair genes and what do they do?

A

-code for proteins whose normal function is to correct errors that arise when cells duplicate their DNA prior to cell division

-mutations in DNA repair genes can lead to a failure in repair, which in turn allows subsequent mutations to accumulate

27
Q

What is gene amplification and what effect does it have/ cancers that is causes?

A

-where a single gene is amplified so there are more copies then there should be in a chromosome
-this means the protein is over expressed and changes the behaviour of the cell
-can be the cause of breast and stomach cancer

28
Q

What is the result of gene mutations if they make too much protein, makes a different protein, or doesn’t make any protein?

A

-too much protein= alters cell structure
-different protein= alters cell function
-no protein= alters cell behaviour

29
Q

What is chromothripsis?

A

-one massive genomic rearrangement during a single catastrophic event in the cells history

30
Q

In what ways can genetic mutations can cause alterations in cell division?

A

-Altering the instructions for cell growth

-Turning off tumor suppressor genes

-Turning on oncogenes

-Altering DNA repair genes

-Causing aneuploidy (a genetic change when chromosomes aren’t separated properly during cell division, resulting in cells with too many or too few chromosomes)

31
Q

What is silencing?

A

A type of epigenetic modification that regulates gene expression in a cell to prevent the expression of a specific gene