Primary Cutaneous Melanoma Diagnosis
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Melanoma Microchapters |
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Diagnosis |
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Treatment |
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2019 AAD Guidelines for management of Primary Cutaneous Melanoma (CM) |
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Primary Cutaneous Melanoma Diagnosis On the Web |
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American Roentgen Ray Society Images of Primary Cutaneous Melanoma Diagnosis |
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Risk calculators and risk factors for Primary Cutaneous Melanoma Diagnosis |
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 |
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| 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) |
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:
Recommended clinical information to be provided to the pathologist
| Class C | |
|---|---|
| Essential |
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| Strongly Recommended |
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| Optional |
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Recommended histologic features of primary cutaneous melanoma for inclusion in the pathology report
| Class A | |
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| Essential |
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| Class B | |
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| Essential |
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| Optional |
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| Class C | |
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| Optional |
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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.
- ↑ 1.0 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.