Diagnostic Approaches to Skin Disease Flashcards

1
Q

Considerations for diagnostic testing

A

Prioritise which tests will help you narrow down differentials
Take an adequate number of good quality samples
Examine efficiently
Be aware of limitations
* False positives
* False negatives

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Diagnostic tests for ectoparasites

A

Coat brushing
Unstained acetate tape
Skin scrapings (deep and superficial)
Trichograms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Diagnostic tests for bacteria

A

Cytology
Microbial swab for culture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Diagnostic tests for fungi

A

Trichograms (dermatophytes on shaft)
Cytology (yeasts)
Wood’s lamp (Microsporum canis)
McKenzie coat brush (dermatophytes for culture)
Microbial swab for culture (yeasts)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Skin surface cytology tests

A

Used to visualise cells and microbes on skin surface
* Direct impression smear
* Cotton bud impression smear
* Acetate tape strip

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Type of lesion for direct impression smear

A

Most/greasy lesions
Ruptured pustule
Skin under crusts
Accessible sites

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Type of lesion for cotton bud smear

A

Ear canals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Type of lesion for stained acetate tape strip

A

Dry lesion
Less accessible locations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Staining for direct impression smear

A

All 3 diff quick solutions
A - Fixative
B - Eosin
C - Methylene blue

Dip method

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Staining for cotton bud smear

A

All 3 Diff-quick solutions
A - Fixative
B - Eosin
C - Methylene blue

Rack method

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Staining for acetate tape strip

A

Only B and C
*Dip method

Or C only
* Pipette

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Fine needle aspirate cytology

A

To visualise skin cells below surface

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Eosinophil granule colour using H&E stain

A

Pink - Eosinophilic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Neutrophil granule colour using H&E stain

A

Granules don’t stain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Basophil granule colour using H&E stain

A

Dark blue - Basophilic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Why do we biopsy the skin?

A
  • To establish a definitive diagnosis that can’t be reached by less invasive testing methods
  • To rule out other conditions
17
Q

What tests are carried out on skin biopsies?

A

Histopathology
* Allows assessment of tissue architecture
* Usually staid with H&E

Tissue Culture
* To culture and identify Bactria/fungi below skin surface

18
Q

When to use sedation/anaesthesia

A

Can generally carry out biopsies under sedation and local anaesthetic
Use GA for biopsies of feet, lips and noses

19
Q

How many samples should you take?

A

Sample a representative range of lesions
Take a minimum of 3 unless solitary lesion
Sample fully developed primary lesions
* Avoid traumatised skin and necrotic crust

20
Q

Samples for alopecia

A

○ Across margin of alopecia
○ Area of maximum hair loss
○ Normal haired skin
Wedge shape across margin is useful

21
Q

Samples for ulcerated skin

A

○ Skin adjacent to ulcer where epidermis is sill intact
Wedge shape across margin is useful

22
Q

Samples for Pustules, vesicles or bullae

A

Remove whole lesion without disruption
Wedge biopsy is best

23
Q

How to prepare sample site

A

Don’t disturb skin surface
○ Clip hair with scissors
○ Do not disturb crust
○ Do not prep or scrub
Unless excisional biopsy of sub cut nodules

24
Q

How to prepare sample site when using LA

A

○ Draw circle around lesion in indelible marker
○ Infiltrate LA into subcutis around periphery of circle
○ Do not exceed maximum volume of LA for patients weight
○ Check efficacy of analgesia by pricking with needle

25
Types of biopsy
Punch biopsy Wedge/ellipse * Excisional * Incisional
26
Punch biopsies
○ Quick and convenient ○ Use 6-8mm biopsy punches routinely 3/4mm for delicate structures ○ Don't destroy/shear sample Rotate in one direction only Hold perpendicular to skin surface Do not reuse blunt punches
27
Wedge/ellipse biopsy
Tissue excised with a scalpel
28
Excisional biopsy
Used for solitary nodules Vesicles Cut all the way around lesion
29
Incisional biopsy
Transition from normal to lesions skin Biopsy of cutaneous masses Used if pathology suspend in deep dermis/subcutis
30
How to handle sample appropriately
Never handle dermis or epidermis * Only handle by subcutis For histopathology ○ Blot blood gently from underside of sample ○ Place promptly into 10% formalin Minimum 10x volume of tissue sample ○ If thin sample Place on stiff card or end of wooden tongue depressor to prevent curling ○ Give pathologist brief history and suspected differential diagnoses
31
Considerations for cutaneous masses
* May not be homogenous ○ Especially if large ○ Incisional or excisional likely to be more representative than punch * If suspect invasive neoplasm ○ Take incisional biopsy fist before attempting removal Helps ensure adequate margins taken when removal performed
32
Considerations for bacterial and fungal culture
* Used for deep and superficial pyoderma, deep fungal infections ○ Less affected by environmental contamination than surface sample * Withdraw antibiotics for 5-7 days, topical antimicrobials 3+ days prior to sampling for bacterial culture