Dermatological diagnostics & interpretation Flashcards
Describe the white paper test.
To look for flea dirt in order to prove flea infestation.
Wet the paper. Comb the animal and put all the hair and dirt on the white paper. Flea dirt consists of ingested blood - will torn to brownish red on the paper.
This test doesn’t work so well on cats because they groom so thoroughly. Always do treatment trial on cats.
Describe using a Wood’s lamp.
To diagnose dermatophytosis.
Only 50-90% of Microsporum canis will florescence so you can’t rule out the disease.
A Wood’s lamp is a UV-lamp. Let it warm/your eyes to adjust.
Shows an Apple-green color on the hair!
Wrong positives can be caused by creams, crusts, keratin…
Describe Fungal cultures.
Using DTM (Dermatophyte test medium).
Sabouraud agar or Sabouraud dextrose agar (SDA) is a type of agar growth medium containing peptones. It is used to cultivate dermatophytes and other types of fungi, and can also grow filamentous bacteria.
Trichogram/Scrape/McKenzie sample taking by using new toothbrush, brush the animal or lesion (if lesional). Press the medium 5-6 times.
Colonies should appear in 14 days in untreated animal.
Inspect daily. Both colony and color change should happen simultaneously. Keep in Dark room. Check daily!
If suitable colony - you need microscope it (Roth).
False-positives in fomite carriers, false negatives if not enough material.
What is the mckenzie technique for fungal culture?
a method used to collect samples for fungal culture
A fresh, unused toothbrush or a sterile brush is used to collect fungal spores and hairs from the coat of the animal. thoroughly brushed for about 2-3 minutes.
The brushing is done all over the body, even if no lesions are visible, as the animal may still be carrying the fungus asymptomatically.
The toothbrush or brush is pressed onto the fungal culture medium (e.g., DTM or Sabouraud dextrose agar) about 5-6 times to transfer spores.
neg
no colony no color change
neg or pos?
neg
color change and colonies but they are grey so thats just environmental contamination. dermatophytes make fluffy white colonies.
pos or neg?
no color change
colonies yes but needs agar color change as well to be pos
neg or pos?
contamination due to grey color
dermatophytes grow white colonies
if youre suspicious do cytology
neg or pos?
pos for dermatophytes
fluffy white colonies with agar color change
whats this
Diascopy: Press the glass slide on the
skin to tell Erythema from hemorrhage
In this pic: erythema multiforma due to drug reaction
Describe Bacterial cultures.
When should you culture? (5)
Must differentiate normal microbiota vs cause of the disease.
When should you culture?
1. rod shaped bacteria on cytology
2. empirical treatment doesn’t work
3. suspicion of resistance (post-operative infections, non-healing wounds, multiple or recent courses)
4. life-threatening infections
5. (furunculosis - other deep infections that require 4-6 week AB treatment duration)
staph. intermedius is one of most common pathogenic bacteria
How to culture?
Primary lesions (like fluid from pustules) vs under the crust/border of an epidermal colarette.
Sterile procedure, don’t contaminate. Try and aspirate pustules to get the contents onto a slide.
Swabs vs biopsy (like in deep infections)
Disc infusion vs MIC for sensitivity testing.
Typically discontinue the antibiotics for sampling for at least a few days. If not, let the lab know that the animal has been on AB.
Describe Skin scrape/trichogram. (6)
- Glass slide + paraffin oil + sample+ cover slide
- not stained
- use low magnification - 5x 10x lens
- close the diaphragm/condensor (gives higher contrast to your sample)
- the lens is NOT to come into contact with the oil
- this is for large things like hair, parasites
Describe Cytology. (8)
- Glass + sample + immersion oil
- STAINED
- strong magnification 100x
- open diaphragm/condensor
- clean the 100x lens with alcohol swab after use!
- for viewing small things like cells, bacteria, malassezia
- Info about inflammation (neutrophils, eosinophils, macrophages). Inflammation can be sterile (even with
pustules) - Eosinophils in cats and dogs with furunculosis/ autoimmune disease.
Tape strip, direct smear, indirect smear via swabs, FNA
Most skin diseases usually have primary disease + secondary infections!
What can we find on skin/ear cytology?
- Keratinocytes
- Bacteria, yeast
- Neutrophils and other inflammatory cells
- 0 (WNL) up to 3+
- Neoplastic cells
- Artefacts
- Direct smear
- Indirect smear (cottin q-tip etc)
- FNA
Tape strip, direct smear, indirect smear via swabs, FNA
You should not have neutrophils on your skin normally, especially cells that have phagosytized bacteria (visible on microscopy).
What are good options to take sample from interdigital region?
Folds of pug?
Crusts on the back?
tape
swab/ q-tip
lift crust up with slide edge then do direct impression smear with slide
mostly rods, some cocci here and there
tx with local AB ear drops
cocci are smaller than rods and are really round
mostly rods, some cocci here and there
malassezia 3+
rods
biofilm clusters can be seen, needs to be cleaned out
What compound can be used to break up biofilm in ears?
acetylcysteine
tris-nac contains this, similar to triz aural
broken cells maybe neutrophils
epithelial acanthocytes or acantholytic cells (a type of kertinocyte)
neutrophils in the background
“Acantholysis is the loss of cohesion between keratinocytes as a result of dissolution of intercellular connections.”
very typical to pemphigus foliaceous case which this is. the most common autoimmune disease in small animals.
leukocytes
neutrophils
lymphocytes (almost no cytoplasm)
macrophages (have cytoplasm space, suspect infection when they are present)