Lecture 15 Flashcards

1
Q

Provide an example of an extrinsic factor that can influence a tissues ability to repair itself:

A
  1. Infection - bacterial 2. Foreign bodies - impede healing by prolonging inflammation 3. Nutritional - poor nutrition/deficiency - protein, Vitamin A and C, Zn and Cu - inhibits collagen synthesis & retards healing
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2
Q

What are the intrinsic factors that can influence tissues ability to repair itself?

A
  1. Poor blood supply - varies from organ to organ 2. Metabolic disturbances - e.g. diabetes 3. Glucocorticoid/steroid therapy - anti-inflammatory and immunosuppressive effects cause weak scar formation due to inhibition of TGF-B 4. Low immune status (systemic) 5. Mechanical factors - increased pressure, torsion or excessive movement causes wound dehiscence (local) 6. Cell type and extent of injury: labile, stable and permanent (local) 7. Location of injury: extensive exudates in body cavities undergo organisation with eventual scarring (adhesions)
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3
Q

Briefly describe the basic steps of healing in most organs:

A
  1. Haemostasis and inflammation in response to tissue injury with removal of damaged and dead tissue 2. Proliferation and migration of parenchymal and CT cells to reconstitute injured area 3. Angiogenesis and granulation tissue formation 4. Synthesis of ECM proteins and collagen 5. Tissue remodelling 6. Wound contraction (fibroblasts > myofibroblasts) 7. Acquisition of wound strength (weeks to months)
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4
Q

Contrast healing of skin by first intention versus second intention:

A

1st intention: typical of surgical incisions with edges closely opposed 2nd intention: edges not closely apposed - wound defect is larger and contamination is worse

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5
Q

What is the first thing that happens in healing by first intention?

A

Rapid (immediate) activation of coagulation pathways

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6
Q

What happens within 24 hours of healing by first intention?

A

Inflammation (neutrophils in fibrin matrix)

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7
Q

What happens in 24-48 hours in first intention healing?

A

migration and proliferation of epithelial cells with BM reconstruction & wound closure

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8
Q

What happens at day 3 of first intention healing?

A

macrophages replace neutrophils, invasion of granulation tissue and angiogenesis. Collagen fibers at incision margins. Epithelial proliferation approaching normal epidermal thickness

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9
Q

How does granulation tissue form?

A

At day 3, primitive granulation tissue (proliferating angioblasts, fibroblasts and myofibroblasts) begin to invade the incision space. FGF2 and VEGF from macrophages, keratinocytes and endothelial cells promote angiogenesis. Endothelial cells express new integrins so they can sprout from pre-existing capillaries. Fibroblasts = migrate and proliferate at the site of injury depositing ECM proteins. PDGF, FGF-2 and TGF-B from inflammatory cells (M2 macrophages) stmulate fibroblasts

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10
Q

Briefly describe the process of angiogenesis:

A
  1. Enodthelial cells activated by angiogenic factors
  2. Proteolysis of BM
  3. Migration of immature EC into woound
  4. Adhesion molecules pull endothelial cells forward
  5. Production of MMP’s initiatiate remodelling
  6. Endothelial cell adhesion to adjacent cells & basal lamina + expression receptor/ligand for leukocyte adhesion cascade
  7. Recruitement of pericytes for smooth muscle cells for final differentiation
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11
Q

What occurs at day five of healing?

A

neovascularisation peaks and migration and proliferation of fibroblasts occurs

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12
Q

What occurs at week 2 of first intention healing?

A

continued collagen accumulation/fibroblast proliferation. A reduction in inflammation and the regression of vascular channels

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13
Q

What happens at 1 month of healing?

A

cellular connective tissue is devoid of inflammatory cells and covered by normal epidermis

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14
Q

What is the biggest difference between first intention and second intention healing?

A

In secondary intention healing the the inflammatory reaction is much more intense. There will be nuch greater amounts of granulation tissue formation. The wound contraction is much greater. There is substantial scar formation and thinning of the epidermis.

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15
Q

Briefly describe how the process of wound contraction occurs:

A

By the end of the first month a scar replaces the incision. The scar is composed of cellular connective tissue, covered by an intact epidermis. The tensile strength progressively increases.

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16
Q

Why is chronic inflammation often characterised by replacement of the affected tissue by fibrosis?

A

T-lymphocytes and other lymphoid cells are the cells that generally predominate in inflammation. These release cytokines (e.g IL-13) and TGF-B and MMPs.

17
Q

How and when does the process of tissue remodelling occur?

A

During first 2 months of healing. Collagen synthesis exceeds collagen degradation. This results in the tensile strength of the skin approaching 70-80% of non-wounded skin (Type III is replaced by type one)

Extracellular matrix deposition depends upon balance between TGF-B (collagen sysnthesis) versus MMP’s (degraded BM and ECM proteins)

18
Q

How can deficient scar tissue formation occur (too little)?

A

Wound dehiscence - mechanical stress

Ulceration - deficient blood supply

19
Q

What is a complication of excessive formatiomn of repair components (provide an example and why it occurs)?

A

Proud flesh - excessive granulation tissue

Hypertrophic scar/keloid: excess collagen/excess scar tissue

Desmoids: exuberant fibroblast proliferation

20
Q

How does formation of contractures occur?

A

Deformities of the wound +/- the surrounding tissue

21
Q

What problem has caused the issue seem below?

A

Exuberant granulation tissue - not possible to rule out neoplasm without cytology

22
Q

Why do keloids form?

A

Excessive collagen Type III formation