Pathology Flashcards

1
Q

Name functions of the skin

A
  • strong barriers to antigens and organisms
  • thermoregulation BV and sweat glands
  • endocrine function UV stimulation of vitamin D
  • protection from UV rays melanin pigment
  • immune function langerhans cells
  • sensory function; touch, temperature and pressure
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2
Q

Describe the normal epidermis

A
  • stratified keratinising squamous epithelium
  • prickle cells prominent desmosomes
  • granular layer rich in keratohyalin granules
  • corneal layer differentiated keratinised cells
  • corneocytes, shed from surface house dust
  • melanocytes found in basal layer
  • langerhans cells
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3
Q

Describe the dermis

A
  • matrix of type 1 and type 111 collagen
  • elastic fibres
  • ground substance hyaluronic acid and chondroitin sulphate
  • papillary dermis is thin and lies just beneath epidermis
  • reticular dermis thicker bundles type 1 collagen
  • reticular dermis contains appendage structures- sweat glands, pilosebaceous units
  • epidermal BM made of laminin and collagen IV
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4
Q

What is hyperkeratosis?

A

Increased thickness of keratin layer

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5
Q

What is parakeratosis?

A

Persistence of nuclei in the keratin layer

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6
Q

What is acanthosis?

A

Increased thickness of epithelium

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7
Q

What is papillomatososi?

A

Irregular epithelial thickening

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8
Q

What is spongiosis?

A

Oedema fluid between squames appears to increase prominence of intercellular prickles. if severe, vesicle filled by oedema fluid develop

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9
Q

Name the four main reaction patterns of inflammatory skin diseases

A
  • spongiotic-intraepidermal oedema eg eczema
  • psoriasiform; elongation of the rete bridges eg psoriasis
  • lichenoid basal layer damage; eg lichen planus and lupus
  • vesiculobullous blistering eg pemphigoid, pemphigus and dermatitis herpetiformis
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10
Q

Describe the pathogenesis of psoriasis

A
  • remains elusive
  • new lesions can arise at sites of trauma (koebner phenomenon)
  • ?complement mediated attack on keratin layer; munro micro abscesses
  • increased epidermal turnover, epidermal hyperplasia
  • ?hereditary factors
  • ? assoc specific HLA types
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11
Q

What are munro micro abscesses?

A

Collection of neutrophils in the upper parts of the epidermis

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12
Q

What are lichenoid disorders?

A
  • conditions characterised by damage to basal epidermis
  • prototypic condition is lichen planus; common
  • itchy flat topped violaceous papules
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13
Q

Describe the histology of lichen planus

A
  • irregular sawtooth acanthosis
  • hypergranulosis and orthohyperkeratosis
  • band like upper dermal infiltrate of lymphocytes
  • basal damage with formation of cytoid bodies
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14
Q

Describe immunobullous disorders

A
  • vesicle and bullae occur as a secondary phenomenon in many skin diseases eg. eczema, herpes virus infection, burns
  • immunobullous diseases have blisters as the primary feature
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15
Q

Name some important examples of immunobullous disease

A
  • pemphigus
  • bullous pemphigoid
  • dermatitis herpetiformis
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16
Q

Describe pemphigus

A
  • rare autoimmune bullous disease
  • sex incidence is equal, usually middle age
  • loss of integrity of epidermal cell adhesion
  • variable severity - occasionally fatal
  • responds to steroids
  • pemphigus has 4 distinct subtypes
17
Q

Describe pemphigus vulgaris

A
  • autoimmune condition
  • IgG auto-antibodies made against desmoglein 3
  • demsogelin 3 maintains desmosomal attachments
  • immune complexes form on cell surface
  • complement activation and protease release
  • disruption of desmosomes
  • end results is acantholysis
18
Q

Describe the appearance of pemphigus vulgaris

A
  • involves skin especially scalp, face, axillae, groin, trunk
  • may affect mucosa eg mouth, resp tract. extensive mucosal involvement may be fatal
  • produces fluid filled blisters which rupture to form shallow erosions
19
Q

Describe bullous pemphigoid

A
  • subepidermal blister
  • no evidence of acantholysis
  • circulating antibodies (IgG) react with a major and or minor antigen of the hemidesmosomes anchoring basal cells to basement membrane
  • the result is local complement activation and tissue damage
  • dermal papillae project into bulla
20
Q

What does histology show for bullous pemphigoid?

A
  • immunofluorescence shows linear IgG and complement deposited around the basement membrane
  • always send early lesions for histology
  • older lesions of pemphigoid show re-epithelialisation of their floor, mimicking pemphigus vulgaris
21
Q

Describe dermatitis herpetiformis

A
  • relatively rare condition
  • autoimmune bullous disease
  • strong association with coeliac disease
  • associated with HLA-DQ2 haplotype
  • intensly itchy lesions symmetrical
  • elbows, knees and buttocks often excoriated
  • hallmark is papillary dermal microabscesses
22
Q

Describe the distribution of acne

A
  • distribution reflects sebaceous gland sites

- face, upper back, anterior chest

23
Q

Describe the aetiology of acne

A
  • increased androgens at puberty
  • ?? increased androgen sensitivity of sebaceous glands
  • keratin plugging of pilosebaceous units
  • infection with anaerobic bacterium corynebacterium acnes
24
Q

Describe the pathophysiology of acne

A
  • sebum produced by sebaceous gland plugs pilo-sebaceous unit
  • keratin and sebum build up to produce comedones (blackheads / whiteheads)
  • rupture causes acute inflammation and foreign body granulomas
25
Q

Describe rosacea

A
  • common condition
  • around 10% prevalence in caucasian adults
  • commoner in females
  • recurrent facial flushing
  • visible blood vessels
  • pustules
  • thickening of skin; rhinophyma
26
Q

Describe the pathology of rosacea

A
  • vascular ectasia
  • patchy inflammation with plasma cells
  • pustules
  • perifollicular granulomas
  • follicular demodex mites often noted
  • allergic reaction to mites?