Determining the Association Between Melanomas and Fields of Melanocytic Dysplasia.


Journal

The American Journal of dermatopathology
ISSN: 1533-0311
Titre abrégé: Am J Dermatopathol
Pays: United States
ID NLM: 7911005

Informations de publication

Date de publication:
01 Feb 2023
Historique:
received: 06 07 2022
accepted: 07 10 2022
entrez: 20 1 2023
pubmed: 21 1 2023
medline: 25 1 2023
Statut: ppublish

Résumé

Some have proposed that melanomas in situ may be associated with fields of melanocytic dysplasia, particularly on sun-damaged skin, whereas others maintain that the atypical junctional melanocytic hyperplasia (MH) at the periphery of melanomas is simply background junctional MH of sun-damaged skin. The biological potential of atypical junctional MH at the periphery of melanomas is uncertain. We examined whether atypical junctional MH was intrinsic to the melanoma itself (ie, melanoma-associated field of melanocytic dysplasia) or was simply the predictable junctional MH associated with long-standing sun exposure. We retrospectively compared 106 cutaneous melanoma excisions without residual tumor with 105 nonmelanoma cutaneous tumor excisions (ie, basal cell or squamous cell carcinomas) without residual tumor. MH with atypia occurred significantly more frequently in melanoma than in nonmelanoma cutaneous tumor excisions (55.7% vs. 24.8%, P < 0.001). Solar elastosis occurred significantly less frequently in melanoma than in nonmelanoma cutaneous tumor excisions; 33.0% of melanoma excisions and 8.6% of nonmelanoma excision samples exhibited no solar elastosis, respectively (P < 0.001). After controlling for solar elastosis using multivariable linear regression, the association between MH with atypia and melanoma excisions remained significant (P < 0.001). Our results, therefore, demonstrate that melanomas were associated with atypical junctional MH that could not solely be accounted for by the extent of sun damage as measured by solar elastosis.

Identifiants

pubmed: 36669071
doi: 10.1097/DAD.0000000000002339
pii: 00000372-202302000-00004
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-92

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Références

Shain AH, Bastian BC. From melanocytes to melanomas. Nat Rev Cancer. 2016;16:345–358.
Duve S, Schmoeckel C, Burgdorf WH. Melanocytic hyperplasia in scars. A histopathological investigation of 722 cases. Am J Dermatopathol. 1996;18:236–240.
Elder DE, Massi D, Scolyer RA, et al. WHO Classification of Skin Tumours. 4th ed Lyon, France: World Health Organization; 2018.
Hendi A, Brodland DG, Zitelli JA. Melanocytes in long-standing sun-exposed skin: quantitative analysis using the MART-1 immunostain. Arch Dermatol. 2006;142:871–876.
Weyers W, Bonczkowitz M, Weyers I, et al. Melanoma in situ versus melanocytic hyperplasia in sun-damaged skin. Assessment of the significance of histopathologic criteria for differential diagnosis. Am J Dermatopathol. 1996;18:560–566.
Barlow JO, Maize J Sr, Lang PG. The density and distribution of melanocytes adjacent to melanoma and nonmelanoma skin cancers. Dermatol Surg. 2007;33:199–207.
Tang J, Fewings E, Chang D, et al. Nature. 2020;586:600–605.

Auteurs

Douglas A Mata (DA)

Foundation Medicine, Inc., Cambridge, MA.

Christine G Lian (CG)

Division of Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, MA; and.

Farhaan Hafeez (F)

Department of Dermatology, St. Luke's University Health Network, Temple University School of Medicine, Bethlehem, PA.

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