Primary Cutaneous Melanoma Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Anum Ijaz M.B.B.S., M.D.[2]

2019 AAD Guidelines for Diagnosis of Primary Cutaneous Melanoma

Recommendations for Diagnostic Biopsy Techniques

Class B
1. Preferred biopsy technique is a narrow excisional/complete biopsy with 1- to 3-mm margins that encompass the entire breadth of the lesion and is of sufficient depth to prevent transection at the base. This may be accomplished by fusiform/elliptical or punch excision or deep shave/saucerization removal to depth below the anticipated plane of the lesion.(Level of Evidence:Ⅱ)
2. Partial/incomplete sampling (incisional biopsy) is acceptable in select clinical circumstances such as facial or acral location, very large lesion, or low clinical suspicion or uncertainty of diagnosis. (Level of Evidence:Ⅱ)
3. Narrow-margin excisional biopsy may be performed if an initial partial biopsy is inadequate for diagnosis or microstaging, but it should not generally be performed if the initial specimen meets the criteria for consideration of sentinel lymph node biopsy. (Level of Evidence:Ⅱ)

[1]

Recommendations for documentation of Pathology Report

Once the biopsy of a suspected lesion is performed, the American Academy of Dermatology(AAD) recommends that information be provided to the pathologist and clinician performing the biopsy, with the notations as illustrated below:

Class C
Essential
  • Age of patient
  • Sex
  • Anatomic location(including laterality)

(Level of Evidence: Ⅲ,Expert Opinion)

Strongly Recommended
  • Biopsy intent (excisional/complete vs partial/incomplete) and technique(elliptical, punch shave/saucerization)
  • Size of lesion
  • Clinical impression/differential diagnosis
  • Macroscopic satellites; Clinical photograph (if possible)

(Level of Evidence: Ⅲ,Expert Opinion)

Optional
  • Clinical description/level of suspicion for melanoma/prior change or biopsy (if applicable)
  • Dermoscopic features (with or without photograph)

(Level of Evidence: Ⅲ,Expert Opinion)

[1]

Class A
Essential
Class B
Essential
Optional
Class C
Optional

[1]

Recommendations for diagnostic, prognostic, and therapeutic molecular testing

Class C
1. Ancillary diagnostic molecular techniques (eg, CGH, FISH, GEP) may be used for equivocal melanocytic neoplasms(Level of Evidence:Ⅲ)
2. Routine molecular testing, including GEP, for prognostication is discouraged until better use criteria are defined. The application of molecular information for clinical management (eg, sentinel lymph node eligibility, follow-up, and/or therapeutic choice) is not recommended outside of a clinical study or trial.(Expert Opinion)
3. Testing of the primary CM for oncogenic mutations (eg, BRAF, NRAS ) is not recommended in the absence of metastatic

disease.|(Level of Evidence:Ⅲ,Expert Opinion)

*BRAF= B-Raf proto-oncogene, serine/threonine kinase gene; CGH= comparative genomic hybridization; CM= cutaneous melanoma; FISH= fluorescence in situ hybridization; GEP= gene expression profiling; NRAS= NRAS proto-oncogene, GTPase gene. [1]

References

Swetter SM, Tsao H, Bichakjian CK, Curiel-Lewandrowski C, Elder DE, Gershenwald JE, Guild V, Grant-Kels JM, Halpern AC, Johnson TM, Sober AJ, Thompson JA, Wisco OJ, Wyatt S, Hu S, Lamina T (January 2019). "Guidelines of care for the management of primary cutaneous melanoma". J Am Acad Dermatol. 80 (1): 208–250. doi:10.1016/j.jaad.2018.08.055. PMID 30392755.

  1. 1.0 1.1 1.2 1.3 Swetter SM, Tsao H, Bichakjian CK, Curiel-Lewandrowski C, Elder DE, Gershenwald JE, Guild V, Grant-Kels JM, Halpern AC, Johnson TM, Sober AJ, Thompson JA, Wisco OJ, Wyatt S, Hu S, Lamina T (January 2019). "Guidelines of care for the management of primary cutaneous melanoma". J Am Acad Dermatol. 80 (1): 208–250. doi:10.1016/j.jaad.2018.08.055. PMID 30392755.