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Superficial Spreading Malignant Melanoma of Skin

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This article should be read in conjunction with the article Malignant Melanoma (All Sites).

Epidemiology
  • Superficial spreading melanoma (SSM) is the most common subtype and it occurs in approximately 70% of patients with a melanoma.1
  • Most common on the trunk in men and on the legs in women.
  • Most often presents in individuals aged 30-50 years.
Presentation

MALIGNANT MELANOMA -SUPERFICIAL SPREADING (DIS107.jpg)

  • Melanomas may arise from otherwise normal appearing skin or from within a mole or freckle, which starts to grow larger and change in appearance.
  • SSM presents as a flat or slightly elevated brown lesion with variegated pigmentation (black, blue, pink, or white discoloration).
  • SSM is usually greater than 6 mm in diameter and has characteristic irregular asymmetrical borders.
  • SSMs tend to grow slowly but at any time they may begin to thicken or develop a nodule and progress to a vertical growth phase.
  • The edge is often scalloped with dark pigment reaching into normal skin.
  • Erythema and scaling are sometimes present but the lesions rarely erode the surface so oozing and bleeding are uncommon.

    MALIGNANT MELANOMA -SUPERFICIAL ELONGATED (DIS104.jpg)


  • There may be areas of regression that are the colour of normal skin, or white and scarred.
  • During its horizontal phase of growth a melanoma is normally flat. As the vertical phase develops, the melanoma becomes thickened and raised.
  • Some melanomas are itchy or tender. More advanced lesions may bleed easily or crust over.

MALIGNANT MELANOMA -CLOSE UP (DIS70.jpg)

Prognosis
  • Prognosis tends to be good if the depth of invasion is low, especially if growth is in the horizontal (radial) phase.
  • Death is unlikely if a melanoma has a tumour thickness (Breslow depth) of less than one millimetre (T1).
  • About half of patients die within 5 years if their melanoma is more than 4 mm thick (T4).

Document references
  1. Swetter SM; Malignant Melanoma. eMedicine, January 2008.
Acknowledgements EMIS is grateful to Dr Colin Tidy for writing this article and to Dr Hayley Willacy for earlier versions. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
DocID: 4060
Document Version: 21
DocRef: bgp25992
Last Updated: 4 Jan 2009
Review Date: 4 Jan 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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