Textbook of Plastic and Reconstructive Surgery

Edited by Deepak M. Kalaskar, Peter E. Butler & Shadi Ghali

Cancer - Skin Cancer for the Plastic Surgeon

4.1. Diagnosis

Clinical suspicion should lead to a tissue diagnosis of malignant melanoma. Guidelines for the recognition of high-risk lesions are the following well-known ‘ABCDE’ criteria:

  • A – Asymmetry

  • B – Border (irregular)

  • C – Colour variety (a number of different shades of brown or black, blue, etc.)

  • D – Diameter (>6 mm diameter)

  • E – Evolving (any change in size, shape, colour, elevation or any new symptom).

Figure 3.2.
The ‘ABCDE’ rule. Source: Skin Cancer Foundation (2013).

Although these criteria are useful, particularly for the public, it is worth remembering that in fact in the early stages malignant melanomas can be <6 mm in diameter and that approximately 5% of malignant melanomas are actually not pigmented.

Table 3.7. Criteria for urgent referral to a local skin cancer multidisciplinary team.

A new mole in adulthood with changing shape, colour, size
Itching or bleeding
Any mole with asymmetry or three or more colours
Any new persistent skin lesion, especially if pigmented and the diagnosis is unclear
A new pigmented line in a nail
A lesion growing under a nail

Source: Marsden et al. (2010).

Accurate diagnosis is dependent on tissue sampling, and an excisional biopsy is recommended after clinical photography. It is not recommended that this is done in primary care: instead, it should be performed by suitable members of the local skin cancer multidisciplinary team. It is appropriate that the lesion is excised in a manner that allows a further wide excision; excision should include the whole tumour with a 2-mm margin of normal skin and a cuff of fat in order to allow an accurate histological confirmation of diagnosis, Breslow thickness and Clark level (Lederman and Sober, 1985; Austin et al., 1996). Incisional or punch biopsy is sometimes acceptable for specific situations such as facial lentigo maligna (melanoma in situ), but this decision should be made under the guidance of the local skin cancer multidisciplinary team.

The Royal College of Pathologists has produced guidelines for the dataset required in histopathological reports (Association of Directors of Anatomic and Surgical Pathology, 1998). These are summarised in Table 3.8.

Table 3.8. Minimum data set required in histopathological description for malignant melanoma.

Clinical informationSite
Procedure (excision, re-excision, punch biopsy)
Macroscopic descriptionContour
Colour
Size of tumour (mm)
Size of excised specimen (mm)
Microscopic descriptionUlcerationPresence or absence
Thickness of the tumourMeasured from the granular layer of epidermis to the deepest dermal malignant cells to the nearest 0.1 mm
Number of mitoses per mm2In the area of greatest mitoses in the vertical growth phase
Histological subtypeSuperficial spreading, nodular, lentigo maligna, acral lentiginous melanoma
Margins of excisionIndicates whether excision is complete at peripheral and deep margins
Pathological stagingTNM staging should be used
Growth phaseInvasive melanoma without a vertical growth phase is microinvasion
Regression
Tumour-infiltrating lymphocytes
Lymphatic or vascular invasion
Perineural infiltrationPrognostic factor
MicrosatellitesIslands of tumour >0.05 mm in the tissue beneath the mass of melanoma, separated by 0.3 mm of normal collagen (Harrist et al., 1984). This is predictive of lymph node metastases
Precursor naevusPresence should be recorded
Clark levelLess reliable than thickness

Source: Marsden et al. (2010).

The Breslow thickness describes how deeply the tumour cells have invaded and is measured using an ocular micrometer from the granular layer of the epidermis to the deepest dermal tumour cells (Breslow, 1970). It is not only an important prognostic factor but also guides clinicians as to the excision margins for wide excision and is one of the criteria used in predicting lymph node metastases.

It is different from Clark levels, which determine the level of anatomical invasion of the tumour cells. Clark levels have been superseded by Breslow thickness, except when the Breslow thickness is <1 mm, when they can offer prognostic value.