More than one shade of pink as a marker of early amelanotic/hypomelanotic melanoma.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Jul 2024
Historique:
revised: 07 03 2024
received: 09 01 2024
accepted: 12 03 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 16 10 2024
Statut: ppublish

Résumé

Amelanotic/hypomelanotic melanoma (AHM) may be difficult to diagnose because of a lack of pigmentation. To evaluate whether dermoscopy can be useful for the diagnosis of early AHM, 133 digital dermoscopic images of lesions histopathologically diagnosed as amelanotic/hypomelanotic superficial spreading melanoma with ≤1 mm thickness (AHSSMs) (n = 27), amelanotic/hypomelanotic non-melanocytic lesions (AHNMLs) (e.g., seborrhoeic keratosis and basal cell carcinoma) (n = 79), and amelanotic/hypomelanotic benign melanocytic lesions (AHBMLs) (e.g., compound and dermal nevi) (n = 27), were dermoscopically assessed by three blinded dermatologists. Using multivariate analysis, we found a significantly increased risk of diagnosing AHSSM versus AHNML and AHBML when the lesion was characterized by the presence of more than one shade of pink (odds ratio [OR] 37.11), irregular dots/globules (OR 23.73), asymmetric pigmentation (OR 8.85), and structureless pattern (OR 7.33). In conclusion, dermoscopy may improve early AHM detection, discriminating AHSSM from amelanotic/hypomelanotic non melanoma lesions.

Identifiants

pubmed: 39412946
doi: 10.1111/1346-8138.17200
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

999-1003

Informations de copyright

© 2024 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association.

Références

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Auteurs

M A Pizzichetta (MA)

Department of Dermatology, University of Trieste, Trieste, Italy.
Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

P Corsetti (P)

Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

I Stanganelli (I)

Skin Cancer Unit, Istituto Tumori Romagna (IRST), Meldola, Italy.
Department of Dermatology, University of Parma, Parma, Italy.

G Ghigliotti (G)

Private Dermatologist, Genova, Italy.

S Cavicchini (S)

Private Dermatologist, Milan, Italy.

V De Giorgi (V)

Department of Dermatology, University of Florence, Florence, Italy.

R Bono (R)

Private Dermatologist, Roma, Italy.

S Astorino (S)

Division of Dermatology, Celio Hospital, Rome, Italy.

S Ribero (S)

Department Medical Sciences, Dermatologic Clinic, University of Torino, Turin, Italy.

G Argenziano (G)

Dermatology Unit, Second University of Naples, Naples, Italy.
Department of Dermatology, University of Padova, Padova, Italy.

J Polesel (J)

Cancer Epidemiology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

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