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

Author:

Pizzichetta M. A.12ORCID,Corsetti P.2,Stanganelli I.34,Ghigliotti G.5,Cavicchini S.6,De Giorgi V.7,Bono R.8,Astorino S.9,Ribero S.10ORCID,Argenziano G.11,Alaibac 12,Polesel J.13,

Affiliation:

1. Department of Dermatology University of Trieste Trieste Italy

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

3. Skin Cancer Unit Istituto Tumori Romagna (IRST) Meldola Italy

4. Department of Dermatology University of Parma Parma Italy

5. Private Dermatologist Genova Italy

6. Private Dermatologist Milan Italy

7. Department of Dermatology University of Florence Florence Italy

8. Private Dermatologist Roma Italy

9. Division of Dermatology Celio Hospital Rome Italy

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

11. Dermatology Unit Second University of Naples Naples Italy

12. Department of Dermatology University of Padova Padova Italy

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

Abstract

AbstractAmelanotic/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.

Publisher

Wiley

Reference15 articles.

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