Dermatopathology Flashcards

1
Q

What is the pathological definition of basal cell carcinoma

A

A group of malignant cutaneous tumours characterised by the presence of lobules, columns, bands or cords of basaloid cells
* most slow growing and non-aggressive

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2
Q

Describe the histopathology of a basal cell carcinoma

A
  • originate from follicular bulge stem cells and basaloid epithelia of follicular projections of anagen hair buds
  • dual population of fibrous stroma and islands of basaloid cells
  • peripheral palisading and haphazard arrangement of cells in centre of islands
  • numerous mitoses and apoptotic bodies
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3
Q

What are the histopathological subtypes of basal cell carcinoma?

A
  • nodular (less risk of recurrence)
  • superficial
  • infiltrative (less cohesive with disparate tumour islands/possible perineural infiltration, increased risk of recurrence)
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4
Q

What would you include in a pathological report for BCC?

A
  • confirmation of diagnosis
  • subtype of BCC
  • whether there is perineural infiltration or not
  • distance to margins
  • pT staging
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5
Q

What is the definition of squamous cell carcinoma?

A

A malignant neoplasm of epidermal keratinocytes in which the component cells show variable squamous differentiation

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6
Q

Describe the histology of squamous cell carcinoma

A
  • nests or islands of squamous cells arising from the epidermis and extending into the dermis or beyond
  • variable keratinisation depending upon differentiation of the tumour (well differentiated = increased keratinisation)
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7
Q

What other differentials do you need to keep in mind when considering squamous cell carcinoma as a diagnosis?

A
  • malignant (BCC, adnexal carcinoma)
  • benign (seborrhoeic keratoses, viral warts)
  • uncertain malignant potential (keratoacanthoma)
  • premalignant/in-situ malignancy (actinic keratosis, Bowen’s disease)
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8
Q

What is included in the pathological report for cutaneous SCC?

A
  • SCC subtype (most are of usual/no specific type)
  • tumour grade
  • level of invasion
  • depth of invasion
  • perineural infiltration
  • lymphovascular invasion
  • resection margins
  • pT staging (UICC TNM8)
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9
Q

Describe the TNM8 clinical classification

A
  • TX: primary tumour cannot be assessed
  • T0: no evidence of primary tumour
  • Tis: carcinoma in situ
  • T1: tumour <20mm or less in maximum dimension
  • T2: tumour >20mm to <40mm in maximum dimension
  • T3: tumour >40mm in maximum dimension or minor erosion or perineural invasion or deep invasion (6+mm in depth or beyond subcutaneous fat)
  • T4a: tumour with gross cortical/marrow invasion
  • T4b: tumour with axial skeletom/skull base/foraminal invasion
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10
Q

What are the criteria for cutaneous SCC MDT referral?

A

1 factor required:
- clinical: site of ear, immunosuppression
- marcoscopic: tumour diameter >20mm
- pathological: poorly differentiated, >4mm thick, >subcutaenous fat, perineural invasion, desmoplastic subtype

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11
Q

What is needed in the pathology report for melanoma?

A
  • tumour subtype
  • breslow thickness
  • presence of ulceration or not
  • mitotic index
  • lymphovascular invasion
  • microsatellite or in-transit metastases
  • perineural infiltration
  • tumour infiltrating lymphocytes
  • regression
  • lymph node involvement
  • distance to margins
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12
Q

What defines the Breslow thickness?

A

Measured from most superficial aspect of granular cell layer (or from base of ulcer) to deepest point of invasion

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13
Q

List the prognostic factors for melanoma

A
  • tumour related (tumour thickness, mitotic rate, ulceration, extent of metastatic disease)
  • LVI (lymphovascular invasion)
  • PNI
  • family history
  • sun exposure, tanning beds
  • molecular mutational gene expression, immunogenetics
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14
Q

Describe BRAF testing and targeted treatment

A
  • for pT4b melanomas
  • for metastatic melanomas including microsatellites
  • qualitative detection of BRAF V600E mutation in DNA extracted from melanoma tissue
  • selects patients for treatment with BRAF inhibitor (vemurafenib)
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15
Q

What characterises psoriasis?

A
  • hyperkeratosis: thickened keratin layer
  • parakeratosis: nuclei within keratin layer
  • acanthosis: thickened epidermis
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16
Q

Describe the granulomatous reaction pattern

A

Characterised by chronic granulomatous inflammation:
- epithelioid cells
- giant cells
- lymphocytes
- plasma cells
- fibroblasts
- non-epithelioid macrophages

17
Q

Describe features of acute generalised exanthematous pustulosis

A
  • rapidly evolving pustules on erythematous background
  • typically starts on face or in armpits and groins
  • following ingestion of certain drugs, resolves on cessation