Difference between revisions of "Skin Immunologic - Pathology"
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===Type I reactions=== | ===Type I reactions=== | ||
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===Type II reactions=== | ===Type II reactions=== | ||
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===Type III reactions=== | ===Type III reactions=== | ||
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===Type IV reactions=== | ===Type IV reactions=== | ||
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==Hypersensitivity reactions== | ==Hypersensitivity reactions== | ||
− | ===Allergic | + | ===[[Allergic Contact Dermatitis]]=== |
− | *Usually involves [[ | + | *Usually involves [[Type IV Hypersensitivity|Type IV reaction]] |
*Pruritic lesions with self-inflicted trauma | *Pruritic lesions with self-inflicted trauma | ||
*At areas in contact with allergen | *At areas in contact with allergen | ||
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**If chronic, epidermal hyperplasia | **If chronic, epidermal hyperplasia | ||
**May involve [[Eosinophils|eosinophils]] | **May involve [[Eosinophils|eosinophils]] | ||
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+ | [[Category:Type IV Hypersensitivity Diseases]] | ||
+ | [[Category:Integumentary System - Hypersensitivity Reactions]] | ||
===Atopy=== | ===Atopy=== |
Revision as of 16:22, 22 February 2011
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General
- Classification:
- Hypersensitivity - response to normally harmless substances
- Auto-immune - antobodies or T-cells reactive against self-antigens
- Mostly involves mixture of types described below
Type I reactions
Type II reactions
Type III reactions
Type IV reactions
Hypersensitivity reactions
Allergic Contact Dermatitis
- Usually involves Type IV reaction
- Pruritic lesions with self-inflicted trauma
- At areas in contact with allergen
- Grossly:
- Erythema, papules, +/- vesicles, exudation -> crusts
- If chronic, lichenification, hyperpigmentation, alopecia
- Microscopically:
- Spongiotic superficial perivascular dermatitis
- Mononuclear cells
- If chronic, epidermal hyperplasia
- May involve eosinophils
Atopy
- Involves Type I reaction
- Mainly causes pruritus
- Dogs - face rubbing and foot licking; secondary pyoderma or seborrhea
- Cats - facial, ear or generalised pruritus, miliary dermatitis, eosinophilic granuloma complex, symmetric alopecia
- Horses - pruritic hea, pinnae, ventrum, legs, tailhead or recurrent urticaria
- Lesions generally due to self-trauma
- Microscopically:
- Hyperplastic superficial perivascular dermatitis
- Mast cells, eosinophils, nonmetachromatic mononuclear cells
- Perivascular inflammation may be involved especially in horses
Culicoides Hypersensitivity
Flea Bite Hypersensitivity
Autoimmune reactions
Bullous pemphigoid
- Dogs and horses
- Involves oral cavity, mucocutaneous junctions, groin and axilla
- Subepidermal vesicles and bullae
- Antibodies bound to basement membrane
- Grossly:
- Similar to Pemphigus vulgaris
- Microscopically:
- Bullae containing fibrin, neutrophils or eosinophils
- Basement membrane forms floor of bullae and roof is lined with basal cells
- Bullae may rupture -> ulcers
Dermatomyositis
- See also Canine dermatomyositis
- Affects puppies of collies and shetland sheepdogs from 8 weeks of age
- Lesions - vesiculating dermatitis
- Face, lips, external ears, later distal extremities
- Microscopically: interface dermatitis and basal cell degeneration of epidermis and follicular wall, atrophy of follicles, epidermal vesicles and pustules, dermal scarring
Lupus erythematosus
- Systemic (SLE)
- Multiple organs involved
- Cats, dogs, horses
- Immune dysregulation:
- Damaged T-cell suppressor function, either primary deficiency or antibody mediated
- Cytokine dysregulation
- Resulting B-cell hyperactivity -> antibodies to self antigens -> antigen-antibody complexes deposited in various tissues -> Type III hypersensitivity
- Lesions localised or generalised
- Erythema, alopecia, depigmentation, crusting and scaling, ulceration
- Microscopically: lymphohistiocytic interface dermatitis, thickened basement membrane, vasculitis, subepidermal vesicles, basal cell degeneration
- Discoid
- Milder variant of systemic
- Depigmentation, erythema, scaling, erosions, ulceration, crusting
- Usually involves nasal planum, dorsum of muzzle, occasionally pinnae, lips, oral mucosa or periocular area
- Microscopically: lichenoid interface dermatitis, often with lymphocytes, plasma cells, basal cell degeneration, loss of pigment