Melanoma classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Yazan Daaboul, M.D.; Serge Korjian M.D.

Overview

Melanoma may be classified into either cutaneous or non-cutaneous melanomas. The most common 4 sub-types of cutaneous melanoma include superficial spreading melanoma, nodular melanoma, acral lentiginous melanoma, and lentigo maligna melanoma. Less common sub-types of melanoma include desmoplastic/spindle cell melanoma, nevoid melanoma, spitzoid melanocytic melanoma, angiotropic melanoma, blue nevus-like melanoma, and composite melanoma.

Classification of Melanoma

Shown below is a table that demonstrates the various sub-classes of melanoma:^[1]^[2]

Subtype	Frequency	Clinical Features
Common Subtypes
Superficial spreading melanoma	70%	Most common sub-type Usually affects sun exposed sites among both men and women aged 50-70 years Characterized by the presence of abundant junctional intra-epidermal 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 the absence of junctional intra-epidermal spread of malignant melanocytes
Acral lentiginous melanoma	5%	Not associated with chronic ultraviolet exposure Affects the extremities of individuals of all races Common among the elderly Caucasian and non-Caucasian individuals
Lentigo maligna melanoma	1-5%	Preceded by lentigo maligna Common among the elderly Caucasian patients Usually appears as a flat, non-palpable lesion that affects sun exposed sites, especially the head and neck (lesions on extremities are 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
Desmoplastic/Spindle cell melanoma	Rare	Lesion typically amelanotic and has a morphology similar to a scar tissue Appears indolent but is highly infiltrative Characterized by local recurrence and perineural spread Usually affects males aged 60-70 years in sun exposed sites May be de novo or can be associated with a pre-existing melanoma Has several subtypes: Pure: paucicellular Desmoplastic-neurotropic melanoma: characterized by neurotropism Pure neurotropic melanoma: 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 a typical melanoma
Spitzoid melanocytic neoplasm	Rare	Lesion has features of both melanoma and Spitz (epithelioid) 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 the 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 sub-type 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 Appears 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 the proximity of 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

↑ Schanderdorf D, Kochs C, Livingstone E (2013). Handbook of Cutaneous Melanoma: A Guide to Diagnosis and Treatment. Springer.
↑ Mooi W, Krausz T (2007). Pathology of Melanocytic Disorders 2nd Ed. CRC Press.

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[book1-1] Schanderdorf D, Kochs C, Livingstone E (2013). Handbook of Cutaneous Melanoma: A Guide to Diagnosis and Treatment. Springer.

[book2-2] Mooi W, Krausz T (2007). Pathology of Melanocytic Disorders 2nd Ed. CRC Press.

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