Derm 9 - more allergies Flashcards

1
Q

How to identify an allergic cat - Hypersensitivity Reaction Patterns
> what are they?
> common patterns?

A
  • cats “like” to do the same thing differently! Feline cutaneous hypersensitivity reaction patterns are various presentations that cats have when they are exhibiting a hypersensitivity reaction.
  • Head and neck pruritus,
  • miliary dermatitis,
  • eosinophilic granuloma complex (eosinophilic granuloma, eosinophilic ulcer, eosinophilic plaque)
  • and feline self trauma
    > are all variations of the same theme
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2
Q

Head and neck pruritus - when to we see it in cats? Ddx?

A
  • “Head and neck pruritus” is a common hypersensitivity presentation of a patient with an adverse food reaction.
  • However, other differentials will include herpes viral dermatitis
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3
Q

Miliary dermatitis in cats - what does it look like, what should we consider?

A
  • If a patient presents with miliary dermatitis, a crusted papular eruption, one should consider flea allergies as it is one of the most common underlying causes.
  • However, there are many other causes that should be considered including food allergies, atopic dermatitis and even dermatophytosis.
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4
Q

Eosinophilic granuloma complex - what is this?
- what is included? what do they look like?

A

a group of hypersensitivity reaction patterns that can present as eosinophilic granulomas, indolent ulcers or eosinophilic plaques
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Eosinophilic granuloma can present in a number of ways, eg:
- “pouty lip”
- linear plaque on the caudal aspect of the hind legs
- plaque-like lesions on the soft palate and tumours under the tongue
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Indolent ulcers (also known as eosinophilic ulcers or rodent ulcers)
- often on lips, Ddx SCC
- may respond to antibiotic therapy
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Eosinophilic plaques
- erythematous, oozing, raised lesions that typically are found on the inner thigh or ventral abdomen
- secondary infection common
- may respond to antibiotic therapy

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5
Q

is feline self-trauma generally a behavioural issue? relationship to allergies, other conditions?

A

In one study:
- 76% had a purely medical etiology
- 57% of the cases in that study adverse food reactions played a role
- 52% were multifactorial
- In 14.3% of the cases, psychogenic alopecia played a role
- Only 9.5% of the cases were purely behavioural in origin.

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6
Q

how to differrentiate flea from non-flea hypersensitivity disease

A
  • Widespread lesions are less supportive of food or fleas
  • multiple reaction patterns make fleas less likely to be the sole cause
  • miliary dermatitis in dorsal distribution more likely flea allergy , but less likely flea related when not in dorsal distribution
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7
Q

Criteria set for the diagnosis of feline NFHD ((NFHD = Non-Flea Hypersensitivity Dermatitides)

A
  1. Presence of at least two body sites affected
  2. Presence of at least two of the four following clinical patterns:
    a) Symmetrical alopecia
    b) Miliary dermatitis
    c) Eosinophilic dermatitis
    d) Head and neck erosions ⁄ ulcerations
  3. Presence of symmetrical alopecia
  4. Presence of any lesion on the lips
  5. Presence of erosions or ulcerations on the chin or neck
  6. Absence of lesions on the rump
  7. Absence of nonsymmetrical alopecia on the rump or tail
  8. Absence of nodules or tumours
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8
Q

is feline self trauma all about allergies? how many cases have non-allergic etiology?

A

In one study (Hobi et al) 24% had a non-
allergic etiology
> Numerous conditions (parasitic, viral, fungal, autoimmune and neoplastic) must be ruled out before a diagnosis of hypersensitivity disease can be confirmed

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9
Q

non-allergic medical causes of feline self trauma

A
  • ectoparasites
  • infectious (dermatophytosis, Malassezia, Herpes
    viral dermatitis, bacterial (rare))
  • Localized: neuropathic pain / idiopathic ulcerative dermatitis
  • utricaria pigmentosa (cutaneous mastocytosis)
  • Cutaneous T-cell lymphoma -
    Mycosis fungoides (exfoliative erythroderma)
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10
Q

viral disease of cat often misdiagnosed as allergy? why?

A
  • Herpes viral dermatitis can easily be misdiagnosed as allergic skin disease
  • It presents as crusted skin lesions, often at the nose and periocular skin. When the crusts are removed, the exposed skin is inflamed and ulcerated
  • On histopathology, the dermis is intensely and diffusely inflamed, usually with eosinophils predominating
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11
Q

(environmental) atopic dermatitis pathogenesis

A
  • Epidermal barrier defects play a significant role but it is unclear in dogs whether there is a primary defect or the defect is secondary to the release of various mediators of inflammation.
    > Regardless, these defects are thought to facilitate percutaneous absorption of environmental allergens
  • The allergens are processed by antigen presenting cells
  • These cells then travel into lymph nodes where they trigger the activation of T-cells and the release of
    cytokines such as IL-4 and IL-13 and subsequent production of allergen specific IgE
  • The activated T cells migrate back to the skin
  • Following sensitization, when Langerhans cells with allergen specific IgE are exposed to the same allergen it can rapidly trigger the activation of T-cells, which in turn release pruritogenic cytokines
  • One of these cytokines, IL-31, has recently become the focus of much research and discussion in the veterinary dermatology community
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12
Q

how are environmental allergies diagnosed?

A

 Diagnosis of exclusion
 Control for parasites, infection, food….

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13
Q

what does a positive allergy test mean? can we make a diagnosis?

A

A positive allergy test, whether performed as an in vivo test or in-vitro test, means that the test was positive; it does NOT mean that allergies are the cause of the itchiness. These tests should never be performed to make a diagnosis

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14
Q

Intradermal skin testing - use

A
  • Intradermal skin tests (IDT) are still considered by most dermatologists to be the gold standard in
    veterinary medicine as it tests the target organ.
  • However, there are cases where in vitro allergy
    testing (IVAT) is indicated.
  • injections of allergens in grid pattern
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15
Q

in vitro allergy testing methodology

A
  • serum is allowed to interact with allergen extract
  • unbound antibodies are washed away
  • allergen bound IgE is detected using a reagent specific for IgE
  • Amount of IgE is quantified
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16
Q

In vitro allergy testing methods, how they work, uses

A

RAST, ELISA: allergend to be tested are attached to a solid substrate (paper disk or polystyrene well)
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VARL: liquid phase immunoenzymatic assay - mixes labelled allergen with patient serum allowing for 3D orientation
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Molecular allergology: using a single allergen component for the detection of IgE rather than allergy extracts, better defining the precise trigger. Some IgE inducing allergens are not clinically relevant.
> this helps to identify cross reaction when both are used
> Cross reactive carbohydrate determinants can be allergenic in some cases and not in others.
Irrelevant CCDs can cause false positives by binding IgE receptors in the test

17
Q

do allergy tests tend to agree with one another, ie. do intradermal tests and serum tests correlate?
- what does this mean for therapies based on these results?

A
  • Most of the in vitro allergy tests available do not correlate with intradermal testing, and those that
    correlate better seem to have more false negatives)
  • serum tests from different labs do not correlate with eachother
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  • Yet, in the hands of veterinary dermatologists, aqueous immunotherapy based on both serum and intradermal testing have good response rates
18
Q

what is “atopic like dermatitis” and do are individuals with this condition respond to allergy testing?
- how common is this?

A

= intrinsic allergies - negative tests in known allergic individuals
> occurs in 20% of canine patients reglardless of the methodology
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Therefore, this test cannot eliminate the possibility of environmental allergies

19
Q

allergen-specific immunotherapy - what are two important factors contributing to success?

A

Choice of the allergens extract and the number to be included in the of them (10-12) is critical!
- be prepared for and comfortable with micro-management and adjustment
- timing of test?

20
Q

the role of geography, pollination period, and allergy testing for results?
for IDT and IVAT

A

There are regional differences. This is not just about choice of allergens but also timing of the test.
> Allergy testing is recommended within 1-2 months of cessation of clinical signs. In regions such as Eastern Canada allergy testing is best performed seasonally
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IDT:
to minimize the risk of a negative skin test, it should be done within 2 months after the end of the allergy season
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IVAT:
IgE levels may be stable for 2 months after the end of the allergy season