Skin structure ,function and infection Flashcards

(11 cards)

1
Q

What are the names of the barriers of the skin

A

There are 4 barriers of the skin .

> Microbiome barrier
Chemical barrier
Physical barrier
Immune Barrier

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2
Q

What is the function of the Microbiome ?

A

> It forms the normal flora
It inhibits the pathogen colonization / proliferation
Hydrolyzes lipids to form epidermal lipids and maintain pH
Regulates keratinocytes cytokine and AMP secretion
Regulates T cell differentiation

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3
Q

What is the function of the chemical barrier

A

1.Acidic pH
>Sustain normal flora and provides conducive environment for production and function of epidermal lipids and antimicrobial substances

2.Antimicobial peptides
>Defensins and cathelicidins are produced by keratinocytes and other cells .There is a differential production in follicular and intrafollicular skin. The antimicrobial peptides function by disrupting microbial cell wall

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4
Q

What is the function of the physical barrier of the skin

A
  1. Stratum basale: Contains mitotically dividing stem cells. Keratins 5 and 14 are major products of basal keratinocytes
  2. Stratum spinosum: (lamellar bodies are formed )Keratins 1 and 10 replace 5 and 14 when basal keratinocytes migrate into the stratum spinosum
  3. Stratum granulosum:(keratohyalin granules=filagrin precursor ) The major product of keratinocytes in this layer is the filaggrin which induces the aggregation of keratins. The lipids from lamellar bodies
  4. Stratum lucidum and corneum : refer to slides
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5
Q

Classification of skin infections

A

1.Superficial
> Impetigo(epidermis ) :Causes loss of the stratum corneum causing lesions and erupt ulcers .Patients do not normally get fever.

> Erysipelas (Epidermis and superficial dermis ): Can extend to deeper dermis .Usually blocks the lymphatic and results in swelling.Patient can get fever . Has boader

2.Deep :
> Cellulitis (extends to subcutaneous layer): Infection spreads to subcutaneous tissue and lacks boarders around infections

> Fascitis ( Extends to superficial and deep fascia ) : Has areas of necrosis because it
disrupts blood vessel plexuses.

> Superficial : Folliculitis (Infection of the hair follicle )

> Deep :
*Furuncle (Extension of folliculitis )

  • Carbuncle : Extension into subcutaneous tissue with multiple abscesses
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6
Q

Discuss the pathophysiology of burns by discussing the zones

A
  1. Zone of coagulation: Area of insult with immediate cells death and coagulation of of cellular necrosis : irreversible damage
  2. Zone of stasis : Damage less severe but microcirculation damaged and therefore stasis occurs .It initially appears viable but may become necrotic after some few days.
  3. Zone of hyperemia Area of vasodilation due to inflammation .In burn >20-25% of body area ,inflammation and neural stimulation can cause the zone of hyperemia to extend to the entire body producing a systemic response
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7
Q

T/F : Ineffective treatment can extend depth of burn through zone of stais and zone of hyperaemia

A

t

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8
Q

Epidermal / First degree burn

A

> Epidermal injury : S.Basale intact
Erythema ,painful ,dry skin ,no blisters ,capillary refill present
Heal spontaneously without scars ,depending on the extend of the injury

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9
Q

Partial thickness (Second degree )

A

> Superficial /Superficial or mid dermal
Epidermis and papillary dermis and almost reticular dermis
Blisters ,erythma ,painful ,capillary refill present / sluggish
*when blisters are removed ,dermis is pink/white

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10
Q

Full thickness (third/ fourth degree)

A
Extend to subcutaneous tissue/
muscle/ bone
•
White/ black (eschar), waxy appearance
no capillary refill or sensation
•
Do not heal spontaneously, scar
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11
Q

Infections in burns

A


Systemic changes

Immunosuppression; increased gut permeability

Disruption of barrier function at site of injury

Depth and extent of burn wound (necrotic tissue)

Early debridement of deep partial thickness or full thickness
wounds

Change in microbiome at the burn margin and donor
sites Plichta et al. al.,

Change in epidermal lipids and antimicrobial peptides
at the burn margin and donor sites Plichta et al. al.,

Possible implications for future treatments

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