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  • Presentation

Dermoscopic Patterns of Nevi and Melanoma Differentiation

Description

The talk explains how dermoscopy helps distinguish benign nevi from melanoma by assessing global patterns, specific structures, and overall organization. Benign lesions usually show symmetry, fewer colors, and orderly patterns, while malignant lesions tend to be asymmetric, multicolored, and disorganized; gray coloration, shiny white lines, atypical networks, irregular dots or globules, and polymorphous vessels are especially concerning for melanoma. The speaker reviews common nevus patterns such as reticular, patchy network, reticular-homogeneous, globular, homogeneous blue, two-component, and multicomponent patterns, noting that these vary with skin type, age, and body location. Congenital nevi often show globular or cobblestone patterns with terminal hairs and perifollicular hypopigmentation, acquired nevi more often show reticular or reticular-globular patterns, blue nevi are typically homogeneous blue, intradermal nevi often have globular homogeneous patterns with comma vessels, and Spitz/Reed nevi may show starburst or radial streaming. The lecture also covers lesions that can mimic melanoma, including traumatized, pink, dysplastic, combined, and deep-penetrating nevi, emphasizing that atypical or changing lesions are often biopsied or excised because dermoscopic overlap with melanoma can be substantial.

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Conclusions

  • Dermoscopy can distinguish benign from malignant melanocytic lesions by evaluating global pattern, symmetry, organization, color count, and specific local structures.
  • Benign nevi usually show ordered, symmetric, and recurrent patterns such as reticular, globular, homogeneous blue, or mixed but symmetric multicomponent patterns.
  • Melanoma is more likely when a lesion is asymmetric, disorganized, multicolored, and shows atypical structures such as off-center blotches, irregular dots and globules, atypical network, or regression features.
  • The meaning of a dermoscopic feature depends on context, because some signs can occur in both benign and malignant lesions but are concerning when focal, asymmetric, or combined with other warning signs.
  • Patient age, skin type, and anatomic location strongly influence the expected dermoscopic pattern of nevi, so interpretation must be adjusted to clinical context.
  • Congenital nevi and nevi with congenital-like features commonly show globular, cobblestone, reticular-globular, diffuse, or multicomponent patterns with hairs, perifollicular changes, or milia-like cysts.
  • Acquired melanocytic nevi more often show reticular or reticular-homogeneous patterns and can evolve with age toward more reticular appearances.
  • Blue nevi are characteristically homogeneous blue lesions, usually with a global pattern of homogeneous pigmentation and little structural complexity.
  • Intradermal nevi often appear as homogeneous globular, pink-tan, or cobblestone lesions with comma vessels and may mimic other benign tumors.
  • Spitz/Reed nevi commonly show a starburst pattern with symmetric radial streaming or pseudopods, but atypical or traumatized lesions can resemble melanoma and may require excision.
  • Pink lesions often have few pigment structures, so vessel morphology becomes especially important for diagnosis, with benign lesions tending to have uniform comma-type vessels and melanoma tending to show polymorphous or irregular vessels.
  • When a lesion displays melanoma-specific dermoscopic features or a pattern that strongly simulates melanoma, biopsy or complete excision is often warranted rather than simple observation.
  • Marghoob, A, Rabinovitz, H. et al. The beauty and the beast sign in dermoscopy. Dermatol Surg. 2007.#10.1111/j.1524-4725.2007.33298.x
  • Zalaudek I, Docimo G, Argenziano G, Using dermoscopic criteria and patient-related factors for the management of pigmented melanocytic nevi. Arch Dermatol 2009;145:816-26.#10.1001/archdermatol.2009.115
  • Antonella Di Cesare, MD, et al. The spectrum of dermatoscopic patterns in blue nevi. Journal of the American Academy of Dermatology (JAAD), 2011.#10.1016/j.jaad.2011.08.018