Patient professional reference
Black and brown skin lesions can be considered as melanocytic neoplasms. The essential task is to exclude malignant melanoma. See also the separate Malignant Melanoma of Skin and Skin Biopsy Techniques in General Practice articles.
Melanomas may have a variety of colours, including tan, dark brown, black, blue, red and occasionally light grey.
Use the 7-point weighted checklist for assessment of pigmented skin lesions:
- Major features of lesions (two points each):
- Change in size.
- Irregular shape.
- Irregular colour.
- Minor features of lesions (one point each):
- Largest diameter 7 mm or more.
- Change in sensation.
- Lesions scoring three points or more in the 7-point checklist above are suspicious (if you strongly suspect cancer any one feature is adequate to prompt urgent referral).
- For low-suspicion lesions, undertake careful monitoring for change, using the 7-point checklist (see below).
- The National Institute for Health and Care Excellence (NICE) recommends ideally making measurements with photographs and a marker scale and/or ruler.
An alternative aide-mémoire to the 7-point checklist described below is the 'ABCDE' list:
- Border irregular.
- Colour irregular.
- Diameter greater than 7 mm.
However, not all these features may be present and, if malignant melanoma cannot be excluded then excision biopsy is required.
- Change in size: naevi may change in size over years but any change over weeks or months is suspicious.
- Change in colour:
- Melanomas often show irregular pigment in a lesion, with shades of black, brown, grey and pink. In nodular melanoma the lesion is often black throughout.
- Rarely, a melanoma can present as a non-pigmented red nodule (amelanotic melanoma), which is more likely on the hands and feet.
- Change in outline: melanomas often show a geographical outline with a sharp cut-off from normal skin.
- Itching may be a late sign and is often unreliable, as many benign naevi intermittently itch.
- Bleeding is also a late sign and is often present in advanced melanoma.
- Melanoma in women occurs more commonly on the extremities and in men on the trunk or head and neck but it can arise from any site on the skin surface.Multiple lesions with irregular pigmentation and edge
Examination of suspicious lesions should include a thorough assessment for other suspicious skin lesions, palpation for regional lymph nodes and examination of the abdomen for enlarged liver and/or spleen.
Nodular melanomaNodular melanoma tends to lack the typical ABCDE melanoma warning signs and therefore may be diagnosed late with a much worse prognosis. Nodular melanomas tend to occur on the heads and necks of elderly sun-damaged men. A nodular melanoma is usually uniform in colour with early ulceration and bleeding.
Multiple cutaneous melanomas
- A minority of patients with melanoma have a second primary melanoma.
- Subsequent melanomas may appear at the same time or up to decades after the first primary melanoma.
- The incidence of a second primary invasive melanoma has been shown to be increased in men and for initial melanoma thickness greater than 2 mm.
- Lesions may be classified as synchronous if they present at the same time or within two months, or metachronous if the second melanoma presents later.
Other causes of pigmented skin lesions
Also called common naevi. See also the separate Intradermal and Compound Naevi article.
Most adults will have approximately 30 moles which they have been acquiring from infancy. Naevi remain static whereas melanoma change in size, shape or colour over weeks or months. New common moles rarely develop after age 40 years and any that do are suspicious.
Typical features of common naevi are:
- Symmetrical in area.
- Even, brown colouring (light or dark).
- Sharp margin.
- <5 mm in diameter.
- Profile varying from flat to pedunculated.
Anyone with >50 moles is at greatly increased risk of malignant melanoma, which may or may not arise from an existing mole. These patients need careful skin monitoring, including baseline skin photography. Any lesion that starts to change colour, bleed, itch, be painful or increase in size needs excisional biopsy.
Also known as dysplastic naevi. They are found in approximately 1 in 12 Caucasians and do not usually become evident until puberty. Unlike melanoma, atypical naevi are usually symmetrical and do not have a sharp edge with geographical border; asymmetry and sharp-edged borders are clear signs of malignant transformation. Atypical moles are easily mistaken for malignant melanoma because of their:
- Lack of symmetry.
- Lack of sharp margin.
- Size >6 mm.
- Variation in colour within the lesion.
Unlike common moles they continue to appear throughout life and occur in areas not often exposed to the sun - eg, buttocks. They are a strong, independent risk factor for malignant melanoma, especially when they are present in numbers (12% risk over ten years). Patients should be very careful with sunlight and undergo regular skin surveillance. Excision of dysplastic naevi is not performed routinely.
See the separate Congenital Pigmented Naevus article.
Very large congenital naevi are known as giant naevi. Patients with large congenital naevi have an increased risk of developing malignant melanoma, often by age 10 years. These appear either within the lesion or as CNS melanoma. Treatment is either excision or close monitoring. Laser treatment is also available.
See the separate Blue Naevus article.
A blue naevus is a small blue or grey lesion, with an appearance similar to a mole. A newly occurring lesion may need excision biopsy to exclude nodular melanoma.
Spitz naevi usually affect the face or limbs of young children. They initially grow rapidly but may then remain static for years. They often disappear spontaneously after a period of time.
See the separate Epidermal Naevus and its Syndromes article.
- Epidermal naevi may be congenital lesions or develop during the early years of life. They tend to grow during childhood and then stabilise during the teenage years. They may be localised to a small area or occur in more diffuse forms.
- Epidermal naevus syndromes are a heterogeneous group of disorders characterised by the presence of one or more congenital hamartomatous ectodermal naevi of the skin with other organ involvement, including brain, eye and the skeleton.
- Becker's naevus: this is a form of epidermal naevus (birthmark). It usually appears around puberty as a hyperpigmented patch, most often found on the upper trunk or shoulders.
See separate Halo Naevus article.
Usually, these consist of a central uniformly pigmented naevus, usually round or oval in shape, with a surrounding area of depigmentation of uniform width from the naevus's edge.
See the separate Junctional Naevus article.
- Junctional naevi are often quite darkly pigmented and are macular or very thinly papular with only minimal elevation above the level of the skin.
- They are an acquired lesion and as they age they can change their characteristics to that of compound naevi.
See the separate Intradermal and Compound Naevi article.
- Compound naevi arise from a flat (junctional) naevus that exists earlier in life. Pigmentation may be uneven within the naevus but is usually symmetrically distributed.
- They are usually of a round/oval shape and roughly 2-7 mm in diameter. They may exist with a variable degree of pigmentation and even be the same colour as the surrounding skin.
See the separate Sebaceous Naevus article.
Usually a single hairless patch (round or linear) is noted on the scalp at birth or shortly afterwards. The classic appearance is velvety tan or yellow-orange.
See the separate Seborrhoeic Wart article.
A flat-topped or warty-looking lesion that appears to be stuck on to the skin. They are usually pigmented, sometimes deeply. They may even be black.
Further reading and references
Revised U.K. guidelines for the management of cutaneous melanoma 2010; British Association of Dermatologists
Suspected cancer: recognition and referral; NICE Clinical Guideline (2015)
Melanoma tests; Cancer Research UK
Chamberlain A, Ng J; Cutaneous melanoma--atypical variants and presentations. Aust Fam Physician. 2009 Jul38(7):476-82.
McCaul KA, Fritschi L, Baade P, et al; The incidence of second primary invasive melanoma in Queensland, 1982-2003. Cancer Causes Control. 2008 Jun19(5):451-8. Epub 2008 Jan 1.
Bataille V, de Vries E; Melanoma--Part 1: epidemiology, risk factors, and prevention. BMJ. 2008 Nov 20337:a2249. doi: 10.1136/bmj.a2249.
Dave R, Mahaffey PJ; Combined early treatment of congenital melanocytic naevus with carbon dioxide and NdYag lasers. Br J Plast Surg. 2004 Dec57(8):720-4.
Skin lesions, tumours and cancers; DermNet NZ
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