37
Introduction to Dermatopathology Peter Pavlidakey, MD

Introduction to dermatopathology

Embed Size (px)

DESCRIPTION

Introduction to Dermatopathology

Citation preview

Page 1: Introduction to dermatopathology

Introduction to Dermatopathology

Peter Pavlidakey, MD

Page 2: Introduction to dermatopathology

Definition of Dermatopathology

• Subspecialty of dermatology and pathology focused on performing and interpreting tests on human tissue samples to provide scientific data and consultative opinions to referring clinicians

• Interpretation of skin biopsies

Page 3: Introduction to dermatopathology

Dermatopathology thought process

• Clinical problem

• Biopsy planning

• Biopsy technique

Page 4: Introduction to dermatopathology

When to perform a skin biopsy

• What can a skin biopsy tell us?

• What are the limitations?

• How do these limitations apply to the clinical scenario?

Page 5: Introduction to dermatopathology

When to perform a skin biopsy

• When is a skin biopsy most likely to be fruitful?

– When it is performed to investigate a focused hypothesis

Page 6: Introduction to dermatopathology

Example: biopsy for alopecia

• Why is she losing her hair?

• Is the etiology of this patient’s hair loss lupus erythematosus or lichen planopilaris?

Page 7: Introduction to dermatopathology

Example: Dermatitis

• Why is this patient’s rash not responding to therapy

• Biopsy out of need

• Is our presumed clinical diagnosis correct or are we in fact dealing with another process?

• Prior therapy?

Page 8: Introduction to dermatopathology

When is a biopsy least likely to yield useful information?

• The biopsy without a clinical hypothesis or in which the clinical hypothesis is not communicated to the dermatopathologist

Page 9: Introduction to dermatopathology

Biopsy planning

• Where to biopsy

• How to biopsy

Page 10: Introduction to dermatopathology

Where to biopsy

• Biopsy the area most likely to distinguish among the considerations or most likely to confirm the primary consideration.

Page 11: Introduction to dermatopathology

Where to biopsy: NMSC

• Preferable to sample entire lesion

• Sample lesion and adjacent normal skin

• Sample entire deep edge of small lesions

Page 12: Introduction to dermatopathology

Best

Better

Worst

Good

Page 13: Introduction to dermatopathology
Page 14: Introduction to dermatopathology

Where to biopsy: Rash

• Sample border of process and unaffected skin

• Different morphologies? – Consider multiple samples

• Prefer new lesions for most conditions –exceptions exist – no substitute for knowledge of process being sampled

Page 15: Introduction to dermatopathology

Worst

BetterBest

Page 16: Introduction to dermatopathology
Page 17: Introduction to dermatopathology

Where to biopsy: Blister

Page 18: Introduction to dermatopathology
Page 19: Introduction to dermatopathology

Biopsy of pigmented lesions

• Dysplastic nevus vs melanoma: elipse, punch, or “scoop” shave – at least 1 mm!

• Try to avoid transecting lesion – peripheral or deep

• Shave-punch vs double shave

• What information will the surgeon and oncologist need?

Page 20: Introduction to dermatopathology

Classification Thickness Ulceration/Mitosis

T1 ≤1.0 mm A: w/o ulceration and mitosis < 1/mm²B: with ulceration or mitosis ≥ 1/mm²

T2 1.01- 2.0 mm A: w/o ulcerationB: with ulceration

T3 2.01- 4.0 mm A: w/o ulcerationB: with ulceration

T4 >4.0 mm A: w/o ulcerationB: with ulceration

Melanoma Staging

Page 21: Introduction to dermatopathology
Page 22: Introduction to dermatopathology

Types of sampling

• Shave

• Punch

• Ellipse

• Curettage

• Extraction

• Fine needle aspiration

• Scraping

• Special sampling for hair and nail

Page 23: Introduction to dermatopathology

Shave biopsy: definition

• Horizontally transects the epidermis

• Usually with a specialized flexible blade or small scalpel

• Deep shave often referred to as saucerizationor “scoop”

Page 24: Introduction to dermatopathology
Page 25: Introduction to dermatopathology

Shave biopsy: Advantages and limitations

• Breadth and depth can be tailored infinitely to the process being sampled

• Ideal for sampling processes restricted to the epidermis and superficial dermis

• Usually neoplasms

• Neoplastic conditions with findings restricted to the epidermis which can be sparse: mycosis fungoides, superficial EAC, PUPPP, etc.

• Potentially excellent cosmesis

Page 26: Introduction to dermatopathology

Punch biopsy

• Uses a specialized cylindrical instrument to vertically transect all levels of the skin

• 1 mm to 1 cm

• Often used to sample dermatitis and selected neoplasms

Page 27: Introduction to dermatopathology
Page 28: Introduction to dermatopathology
Page 29: Introduction to dermatopathology

Punch biopsy: Advantages and limitations

• Potentially samples all layers of the skin

• Much quicker than ellipse

• Variety of sizes available: balance sampling and cosmesis

• Potential to under sample and miss sparse findings

Page 30: Introduction to dermatopathology

Punch biopsy: Tips and techniques

• Use the smallest size which will adequately sample the disease process

• Use 6 mm or larger to sample subcutis

• Never sample suspected panniculitis with 2 mm punch!

• >3 mm preferred to sample dermatitis

• Do not use crushing instruments to extract the sample

Page 31: Introduction to dermatopathology

Ellipse

• Incision to subcutis

• Incisional or excisional

Page 32: Introduction to dermatopathology
Page 33: Introduction to dermatopathology

Ellipse: Advantages and limitations

• Greatest potential for one step management

• Excellent cosmesis with good technique and planning

• Least likely to yield false negative or uninformative result

Page 34: Introduction to dermatopathology

If all else fails…

• Use shaves to sample neoplasms

• Use punches to sample rashes

• Consider elliptical excisional biopsy to sample when suspicion for malignancy is high.

Page 35: Introduction to dermatopathology

Specimen labeling and handling

• Patient identifiers in duplicate

• Precise site designation in duplicate

• State the clinical hypothesis

• Indicate type of procedure and intent of procedure

• Indicate desire for margin evaluation

• Minimize requests of adjuvant diagnostic testing

Page 36: Introduction to dermatopathology

Submit a clinical photo

Page 37: Introduction to dermatopathology

Thank you

Dr Kim Hiatt Dr Peter Pavlidakey