Dog and Cat 3 Flashcards
What is the pathogensis of canine atopic dermatitis
- Not inhaled by actually route via percutaneous
○ Primary defect in your skin barrier -> allows allergens to get access to yours skin -> large exposure to allergens result in allergic response
§ Allergens especially allergens and dust mites could also be food allergy
§ Increase colonisation of bacteria such as staphylococcus that break down skin further and produce antigens that result in production of danger signals
□ Microbiome changes on the skin -> don’t get dampening down of danger signal (IL33, IL25) -> result in TH2 -> IgE production
OVERREACTION OF THE IMMUNE RESPONSE
What are 5 factors that contribute to the atopic phenotype
- High IgE responder
- Low ceramide (lipid production in the skin)
- Low filaggrin expression (helps with sticking skin together)
- Claudin 1 mutation (retain water within the skin)
- TLR-2 mutation
What are the 5 components of atopy
different components based on individual genome
1. Allergy
2. Barrier dysfunction
3. Infections
4. Behaviour
○ Itching behaviour can become a habit more likely to itch
○ Highly anxious dogs are more likely to clinically present as itching
5. Itch
○ Pathogenesis within the skin
○ Midbrain response -> itch or not to itch??
§ Itch to create mild pain signal to inhibit the itch pathway
□ If won’t stop then -> anxious dog, habit or infection
®Anxious dogs have high serotonin levels which inhibit the pain inhibitory pathways therefore keep itching
◊ IN THIS CASE NEED BEHAVIOUR DRUGS
What increases the risk of developing atopy
- Urban life
- High human population density
- Increased average annual rainfall
- Adoption at the age of 8 to 12 weeks
- Regular bathing of young healthy dogs
○ Wash as infrequently as possible
○ Medicated shampoos should be used
Describe the clinical presentation of the 3 levels of severity for atopi dermatitis
- Mild -> Disease in armpits, groin, ears, feet (moist areas) -> more effective skin barrier, most of the skin normal
- Moderate -> allergen penetration where skin isn’t moist -> everywhere that touches the ground -> less effective skin barrier
- Severe -> generalised disease all over the skin
Can get very bad
Atopic dermatitis diagnosis what are the 3 main things involved
- Signalment
- Clinical signs
○ Generally present before 3 years old
○ Itchy and licking - face, leg and ventral abdomen - Exclusion of other DDx
○ Blood test for sensitisation DOESN’T WORK
Diagnostic check list for atopic dermatitis
a. Could this be infection? -> multiple infections?? -> generally have secondary infection due to allergy
b. Could this be demodex? -> primarily not itchy disease but would be if infected
c. Could this be scabies? -> ALWAYS ON THE DIFFERENTIAL LIST
d. Could this be fleas? -> possible
e. Could this be contact allergy?
f. Could this be food allergy? -> NEEDS TO BE CONSIDERED
§ First symptom for food allergy dogs -> Ear infections
g. If this is atopy can I manage this or should I refer?
Outline a diagnosic plan for atopic dermatitis
Step 1
- Resolve infection - DON’T MISS MRSP
○ If 2 weeks on antibiotics and not resolving -> CULTURE
- Bravecto/Nexgard/simpatico to rule out scabies/flea/Demodex
Step 2
- Still itchy when infection free and on isoxazolines - eliminated above
- Where itchy?
1. Contact areas affected = contact avoidance trail
2. Classical atopic areas = food elimination trial - BEEF most common food allergy in dogs,
In terms of contact avoidance trails what is involved in the 3 types of dermatitis
1) Allergic contact dermatitis
- When moving through areas that have these allergens and come into contact with
- AVOIDABLE ALLERGENS -> keep off grass
○ Test to see whether dogs better if off of the grass for 3-4 days
2) Pollen atopic dermatitis
- Exposure through the skin and the pollen comes to you through the air
- NON-AVOIDABLE ALLERGENS
3) Atopic dermatitis
- Pollen, mites, fungi, bacteria
- NON-AVOIDABLE ALLERGENS
In terms of a food elimination trail what should you feed - list 5 options
1) Hydrolysate diets -> Z/D royal canine etc -> inadequate
2) Restricted antigens diets -> extra things within, cross-contamination -> possible fail or food trial
3) Home-cooked diet -> novel protein +/- novel carbohydrate BUT WHAT IS NOVEL
® Cross-reactivity -> lots present within mammalian proteins, fish proteins -> if allergic to one thing may react to others
4) Anallergic diet -> royal canin - NO CROSS-CONTAMINATION
5) Crocodile meat -> LEAST cross-reactivity than other meats such as poultry and- NOT FULL PROOF
In terms of a food elimination trail how long should you do it for and what is needed long term
□ Treat infection and flea control before start
□ MINIMUM 8 weeks
□ Total compliance needed -> try not to give any medications during this time
□ Anti-pruritic (oclacitinib - apoquel) can give with food trial but not all prednisolone
□ Re-assess BEFORE rechallenge and IF flare reported or after 14 days if no flare
□ Sequential rechallenge
What are 6 important questions to ask with history with skin lumps and bumps
- When did you first notice it ○ Is this reliable - Has it changed - Painful or irritating - Any other masses (now, previously) - Other concerns - UV exposure risk
What are important things to look for with physical exam in approaching lumps and bumps
- Signalment
○ Breed predispositions, UV exposure risk - Size - measure, can use your fingers as in-built callipers
- Location - be specific (leg is not specific)
○ Cutaneous vs subcutaneous - As move skin does mass move within
○ UV associated tumors - Fixed or mobile
- Appearance, texture
○ Round/irregular, raised/flat, pigmented, ulcerated, oedematous, firm/soft - Any other masses on skin
- Lymph nodes
○ Which one is the draining lymph node - assess that
Diagnosis based on looks what skin lumps can you do with and what look like
1. Sebaceous adenoma/hyperplasia ○ Old dog warty appearance 2. Papilloma ○ Multiple in young dog 3. Fibropapilloma (skin tag) 4. Dermal Haemangiosarcoma - can be UV associated (sunbathing on ventral surface) 5. Squamous cell carcinoma ○ Appearance, breed disposition, location 6. Lipoma? - CANNOT Need to FNA it
What are the 2 main diagnostic tests for lumps and what information does it provide
1. FNA and cytology ○ Needle off versus needle on ○ Screen slides § +/- definitive diagnosis, if not then: § Is it diagnostic for a clinical pathologist -> are there enough cells to make a diagnosis 2. Histopathology ○ Diagnosis ○ Margins ○ Other prognostic factors if applicable
What are the 3 main options post diagnosis with lumps
- Surgery - in general for localised cancer is the best treatment
- Other
○ Radiation therapy - alone or adjuvant
○ Chemotherapy - alone or adjuvant - No treatment - still needs monitoring
○ Like sebaceous adenomas
Canine cutaneous MCT presentation - what age and growth
- Breeds: boxers, retrievers, pugs, boston and pit bull terriers
- Can occur in young dogs
- Often slow growing, can vary
○ Changes day to day suggestive of MCT, due to histamine
§ Swell one day then decrease the next - repeat
○ Rapid growth, ulceration, systemic signs, suggestive of aggressive disease
Canine cutaneous MCT what are the 2 main locations and diagnostic testings
Location
1. Muzzle/perioral
○ More likely to have LN metastasis at diagnostic than other sites
2. Subcutaneous
○ Unlikely to have aggressive behaviour
○ Some features may be predictive
Diagnosis
1. FNA usually diagnostic
○ Poorly granulated may be more challenging
○ May be suggestive of high vs low grade
2. Staging tests
○ Lymph node assessment recommended in every case
○ +/- ultrasound, liver, spleen FNA
If clinically aggressive features, cytology suggests high grade
Canine cutaneous MCT list the 4 main prognostics factors
1) histolgic grade
2) margins
3) other histopathology features
4) stage - prognostic
Describe the prognostic factor of canine cutaneous MCT histologic grade and margins
- Histologic grade
○ Two vs three-tiered systems
○ Low = better
§ 15-20% of low grade tumors may still have more aggressive behaviour
□ Therefore not necessary tells you the behaviour - Margins
○ Helps to predict risk of local regrowth but not 100% predictive - NOT METASTISE
§ Many low grade tumors never recur, some high grade tumours recur even through complete margins
Describe how other histopathology features and staging helps with prognosis fro canine cutaneous MCT
- Other histopathology features
○ Mitotic index/mitotic rate
§ Per TEN high power fields, should be reported for every MCT
□ 0 = very good, predict benign behaviour
□ 7 = definitive for aggressive behaviour - depending on the scheme used
○ Other additional tests - unclear how to apply them
§ If all come back bad most likely bad and vice versa - Stage - prognostic
○ Distant metastasis
§ Metastasis -> grave prognosis
○ Lymph node metastasis
§ Still local disease -> can get good outcome for aggressive treatment
What are the 3 main treatments for Canine Cutaneous MCT
- Local
○ Surgery
§ Wide vs planned marginal exicison
§ Only do if can excise ALL THE VISIBLE tumor
○ Radiation therapy - Systemic (chemotherapy)
○ Adjuvant for high-risk tumours
○ Known distant metastasis
○ Non-surgical primary tumour (+/- radiation therapy) - Supportive care medications
○ Anti-histamines - with every case
§ Don’t need to do before FNA
§ Should do before surgery -> needs time to take affect
○ Antacids - histamine can lead to stomach ulceration
§ If large and ugly then use this as well
○ Any bulky MCT
Feline MCT what are the 3 main sites and which are more likely
- Primary sites: skin > spleen (in dogs would be metastasis from skin) > GIT
1) Cutaneous
2) feline splenic MCT
3) Feline GI MCT
Cutaneous feline MCT general character, how many generally present and treatment
○ Most are benign, histopathology does not always correlate well with behaviour
§ Histiocytic subtype in young cats may regress
○ Multiple = associated with splenic MCT
§ Staging recommended
○ Treatment: surgery for all