psoriasis Flashcards

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1
Q

what is psoriases?

A

Chronic, genetically determined, immune-mediated, inflammatory skin condition, characterised by typically well defined, scaly plaques. It can also involve nails, hair and joints

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2
Q

What is the epidemiology of psoriases?

A

3% of uk pop. M=F
peak incidences- 20s, 50s
uncommon in Far East population, native Americans, west africans.

many have family history.

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3
Q

Complications?

A

5% develop psoriatic arthritis
psychosocial implications
systemic disease, link to metabolic syndrome and CV disease

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4
Q

How does it present?

A

red scaly plaques
often symmetrical distribution

chronic plaque
flexural
acute guttate
scalp
palmoplanter
nail
pustular
erythrodermic
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5
Q

What causes it?

A

overactivity of the immune system
excessive production of the TH1 cytokine inc TNF-alpha
-vascular proliferation (erythema), increase cell turnover (plaques and scaling)

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6
Q

RF?

A
  • genetics
  • environmental
    infection: strep, candida
  • drugs- lithium, beta blocker, NSAIDs, steroid withdrawal
  • Trauma- kobner phenomenon (spread with trauma
  • sunlight
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7
Q

What are the 3 main pathogenesis?

A
  • Epidermal imnfiltartion by activated T cells
  • Genetics
  • Precipitants
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8
Q

explain epidermal infiltration by T cells?

A
  • there is increase epidermal cell proliferation and turnover- cell cycle reduced from 28 days to 3-5 days, capillary angiogenesis.
  • -exsessive production of TH1 cytokines esp TBF-alpha linked to flares
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9
Q

explain the genetics linked to to pathogenesis?

A
  • Familuy history
  • 1 parent has psoriases= 14% of child developing
  • both parents have = 41% chance
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10
Q

what genes have a link to psoriases?

A

-HLA Cw6, B13, B17

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11
Q

factors that make psoriasis worse? (precipitant factors)

A
trauma
infection
drugs- beta blockers, lithium
sunlight
stress
cigarettes
alcohol
HIV
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12
Q

Histology in psoriases?

A

Hyperkeratosis (thickening of stratum corneum) with parakeratosis (keratinocytes with nuclei in stratum corneum)
Neutrophils in stratum corneum (munro’s microabcesses)
Hypogranulosis: no granular layer (needed for barrier function)
Psoriasiform hyperplasia: Acanthosis (thickening of squamous cell layer) with elongated rete ridges

Dilated dermal capillaries
Perivascular lymphohistiocytic infiltrate; T cell infiltration

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