Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Classification of Melanoma
Subtype
|
Frequency
|
Clinical Features
|
Common Subtypes
|
Superficial spreading melanoma |
70% |
- Most common subtype
- Usually affects sun exposed sites among both men and women aged 50-70 years
- Characterized by presence of abundant junctional intraepidermal spread of malignant melanocytes
|
Nodular melanoma |
15-25% |
- Second most common subtype
- Usually affects sun exposed sites among both men and women aged 50-70 years
- Characterized by absence of junctional intraepidermal spread of malignant melanocytes
|
Acral lentiginous melanoma |
5% |
- Not associated with chronic ultraviolet exposure
- Affects the extremities among inidividuals of all races
- Common among elderly Caucasian and non-Causasian individuals
|
Lentigo maligna melanoma |
1-5% |
- Preceded by lentigo maligna
- Common among elderly Caucasian patients
- Usually appears as a flat, non-palpable lesion that affects sun exposed sites, especially the head and neck (extremities less common)
|
Non-cutaneous melanoma |
5% |
- Melanoma that does not affect the skin
- Usually affects the eye (ocular melanoma) or the mucus membranes (mucosal melanoma)
|
Less Common Subtypes
|
Spindle cell melanoma |
Rare |
- Lesion typically amelanotic
- Appears indolent but is highly infiltrative
- Characterized by local recurrence and perineurial spread
- Usually affects males aged 60-70 years in sun exposed sites
- May be de novo or associated with a pre-existing melanoma
- Has several subtypes:
- Pure: paucicellular
- Desmoplastic-neurotropic melanoma: characterized by neurotropism
- Pure neutrocropic: no desmoplasia with spindle cell melanoma of neurotropic phenotype
- Mixed/Combined: epithelial and spindle cells
|
Nevoid melanoma |
Rare |
- Lesion has features of both melanoma and melanocytic nevus on histopathological analysis
- Clinical features resemble those of typical melanoma
|
Spitzoid melanocytic neoplasm |
Rare |
- Lesion has features of both melanoma and Spitz tumor
- Typically affects sun exposed sites among children and young adults, but adults with Spitz tumors are more often diagnosed with Spitzoid melanoma
- Compared to benign Spitz tumors, Spitzoid melanomas are usually large (>5 mm)
|
Angiotropic melanoma |
Rare |
- Lesion characterized by angiotropism, whereby melanoma grows in proximity (within 1-2 mm) to blood and/or lymphatic tissue but no tumor within the vascular lamina itself
- The tumor may originally be another subtype of melanoma
- Clinical features similar to typical melanoma
|
Blue nevus-like melanoma |
Rare |
- Melanoma that develops from a pre-existing blue nevus
- One of the rarest forms of melanoma
- Appear as a blue nevus that has recently been rapidly expanding with irregular contours
- Typically affects middle-aged men
|
Composite melanoma |
Rare |
- Melanoma that develops in proximity to other pre-existing epithelial malignancies (e.g. basal/squamous cell carcinoma)
- May be characterized by one of the following:
- Collision tumor: Collision of melanoma and another nearby malignant tumor
- Colonization: Colonization of melanocytes in a tumor
- Combined: Two distinct tumors appear to have mixed features of the melanoma and the other tumor
- Biphenotypic: One tumor that has features of melanoma and another epithelial malignancy
|
References
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