TOPIC · SUBTYPE
MECHANISM · DETAILS
FEATURES
CLUE
UV (intense intermittent), fair skin, many or dysplastic nevi, family history (CDKN2A/p16), xeroderma pigmentosum, immunosuppression
Can arise de novo or from a nevus
Childhood sunburns matter most
Features of disordered growth
Asymmetry, Border irregular, Color variation, Diameter > 6 mm, Evolution
"Ugly duckling" lesion
Radial: spreads within epidermis/superficial dermis · vertical: invades deep dermis as a nodule
Radial phase can't metastasize; vertical phase can
Vertical phase = metastatic potential
Depth and spread
Breslow thickness (mm from granular layer to deepest cell), ulceration, mitotic rate, sentinel node
Thin (< 1 mm) → excellent
Superficial spreading
most common
Long radial phase; BRAF V600E common
Trunk (men), legs (women); intermittently sun-exposed skin
Flat irregular multicolored lesion
Early vertical growth
Rapidly growing dark (or amelanotic) nodule; may ulcerate
Worst prognosis of the subtypes
Long radial phase on chronically sun-damaged skin
Elderly; large flat irregular brown patch on face
Best prognosis
Not UV-related; KIT mutations
Palms, soles, nail beds (Hutchinson sign: pigment spreading to nail fold)
Most common type in darker skin
Uveal: GNAQ/GNA11
Uveal melanoma spreads to the liver
Most common primary intraocular tumor in adults
S100, HMB-45, Melan-A, SOX10
Lymph nodes, then anywhere: lung, liver, brain (hemorrhagic), heart, GI, skin
Late recurrences possible
Excision + targeted/immune therapy
Wide local excision, sentinel node biopsy; BRAF inhibitors (vemurafenib, dabrafenib) + MEK inhibitors (trametinib); PD-1 (nivolumab, pembrolizumab), CTLA-4 (ipilimumab)
Checkpoint inhibitors → immune-related colitis, hepatitis, endocrinopathies