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ALL / Dermatology

Malignant melanoma

Malignant melanoma

There are four main subtypes of melanoma. Nodular melanoma has the worst prognosis due to early vertical growth whilst the other forms tend to have an initial radial growth phase.

Superficial spreadingNodularLentigo malignaAcral lentiginous
Frequency70% of casesSecond commonestLess commonRare overall (but most common in people with darker skin)
Typically affectsArms, legs, back and chest, young peopleSun exposed skin, middle-aged peopleChronically sun-exposed skin, older peopleNails, palms or soles
AppearanceA growing mole with diagnostic features listed aboveRed or black lump which may bleed or ulcerateA slowly enlarging pigmented macule/patchSubungual pigmentation (Hutchinson's sign) or on palms or feet


There are other rare forms of melanoma including desmoplastic melanoma, amelanotic melanoma, or melanoma arising in other parts of the body such as ocular melanoma.

The main diagnostic features (major criteria):
  • Change in size
  • Change in shape
  • Change in colour
Secondary features (minor criteria)
  • Diameter >= 7mm
  • Inflammation
  • Oozing or bleeding
  • Altered sensation

Additional commonly used criteria (ABCDE):
  • Asymmetry
  • Border irregularity
  • Colour variation
  • Diameter >6mm
  • Evolving lesion

Treatment
  • Suspicious lesions should undergo excision biopsy with a narrow margin (approximately 2mm). The lesion should be removed completely. Incision biopsy is avoided unless the lesion is large or in a difficult anatomical site.
  • Once the diagnosis is confirmed the pathology report should be reviewed (Breslow thickness is the most important prognostic factor; ulceration is also important) to determine further management:

Margins of excision - related to Breslow thickness
Melanoma in situ0.5cm
Lesions ≤1mm thick1cm
Lesions 1-2mm thick1-2cm (depending on site)
Lesions >2mm thick2cm

Further management
  • Sentinel lymph node biopsy:
    • Offered for Breslow thickness ≥1mm
    • Consider for 0.8–1mm if high-risk features (e.g. ulceration)
  • Imaging: if clinically indicated (e.g. suspected metastases)
  • Adjuvant therapy (stage II–III or high-risk disease):
    • Anti-PD-1 immunotherapy (e.g. pembrolizumab, nivolumab)
    • Targeted therapy (BRAF/MEK inhibitors) if mutation-positive
  • Lymph node management:
    • Completion lymph node dissection is no longer routine after positive sentinel node
    • Nodal surveillance ± systemic therapy is preferred
+PassMedicine Notes

There are four main subtypes of melanoma. Nodular melanoma has the worst prognosis due to early vertical growth whilst the other forms tend to have an initial radial growth phase.

_ Superficial spreading _ Nodular _ Lentigo maligna _ Acral lentiginous | Frequency _ 70% of cases _ Second commonest _ Less common _ Rare overall (but most common in people with darker skin) | Typically affects_ Arms, legs, back and chest, young people _ Sun exposed skin, middle-aged people _ Chronically sun-exposed skin, older people _ Nails, palms or soles | Appearance _ A growing mole with diagnostic features listed above _ Red or black lump which may bleed or ulcerate _ A slowly enlarging pigmented macule/patch_ Subungual pigmentation (Hutchinson's sign) or on palms or feet |

There are other rare forms of melanoma including desmoplastic melanoma, amelanotic melanoma, or melanoma arising in other parts of the body such as ocular melanoma.

The main diagnostic features (major criteria):
  • Change in size
  • Change in shape
  • Change in colour_
Secondary features (minor criteria)
  • Diameter >= 7mm
  • Inflammation
  • Oozing or bleeding
  • Altered sensation|
Additional commonly used criteria (ABCDE):
  • Asymmetry
  • Border irregularity
  • Colour variation
  • Diameter >6mm
  • Evolving lesion
Treatment
  • Suspicious lesions should undergo excision biopsy with a narrow margin (approximately 2mm). The lesion should be removed completely. Incision biopsy is avoided unless the lesion is large or in a difficult anatomical site.
  • Once the diagnosis is confirmed the pathology report should be reviewed (Breslow thickness is the most important prognostic factor; ulceration is also important) to determine further management:

Margins of excision - related to Breslow thickness

Melanoma in situ_ 0.5cm| Lesions ≤1mm thick_ 1cm| Lesions 1-2mm thick_ 1-2cm (depending on site)| Lesions >2mm thick_ 2cm| Further management
  • Sentinel lymph node biopsy:
    • Offered for Breslow thickness ≥1mm
    • Consider for 0.8–1mm if high-risk features (e.g. ulceration)
  • Imaging: if clinically indicated (e.g. suspected metastases)
  • Adjuvant therapy (stage II–III or high-risk disease):
    • Anti-PD-1 immunotherapy (e.g. pembrolizumab, nivolumab)
    • Targeted therapy (BRAF/MEK inhibitors) if mutation-positive
  • Lymph node management:
    • Completion lymph node dissection is no longer routine after positive sentinel node
    • Nodal surveillance ± systemic therapy is preferred


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