Long-Term Sequential Digital Dermoscopy of Low-Risk Patients May Not Improve Early Diagnosis of Melanoma Compared to Periodical Handheld Dermoscopy

Author:

Borroni Riccardo G.12ORCID,Panasiti Vincenzo34,Valenti Mario12,Gargiulo Luigi12,Perrone Giuseppe45ORCID,Dall’Alba Roberta3,Fava Clarissa3,Sacrini Francesco2,Mancini Luca L.2,Manara Sofia A. A. M.6,Morenghi Emanuela17,Costanzo Antonio12

Affiliation:

1. Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini, 4, 20072 Pieve Emanuele, Italy

2. Dermatology Unit, Humanitas Research Hospital—IRCCS, Via Alessandro Manzoni, 56, 20089 Rozzano, Italy

3. Department of Plastic Surgery and Dermatology, Università Campus Bio-Medico di Roma, Via Alvaro del Portillo, 21, 00128 Rome, Italy

4. Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo, 200, 00128 Rome, Italy

5. Department of Pathology, Università Campus Bio-Medico di Roma, Via Alvaro del Portillo, 21, 00128 Rome, Italy

6. Pathology Unit, Humanitas Research Hospital—IRCCS, Via Alessandro Manzoni, 56, 20089 Rozzano, Italy

7. Biostatistics Unit, Humanitas Research Hospital—IRCCS, Via Alessandro Manzoni, 56, 20089 Rozzano, Italy

Abstract

Sequential digital dermoscopy (SDD) enables the diagnosis of a subgroup of slow-growing melanomas that lack suspicious features at baseline examination but exhibit detectable change on follow-up. The combined use of total-body photography and SDD is recommended in high-risk subjects by current guidelines. To establish the usefulness of SDD for low-risk individuals, we conducted a retrospective study using electronic medical records of low-risk patients with a histopathological diagnosis of cutaneous melanoma between 1 January 2016 and 31 December 2019, who had been referred and monitored for long-term follow-up of clinically suspicious melanocytic nevi. We sought to compare the distribution of “early” cutaneous melanoma, defined as melanoma in situ and pT1a melanoma, between SDD and periodical handheld dermoscopy in low-risk patients. A total of 621 melanomas were diagnosed in a four-year timespan; 471 melanomas were diagnosed by handheld dermoscopy and 150 by digital dermoscopy. Breslow tumor thickness was significantly higher for melanomas diagnosed by handheld compared to digital dermoscopy (0.56 ± 1.53 vs. 0.26 ± 0.84, p = 0.030, with a significantly different distribution of pT stages between the two dermoscopic techniques. However, no significant difference was found with respect to the distribution of pT stages, mean Breslow tumor thickness, ulceration, and prevalence of associated melanocytic nevus in tumors diagnosed on periodical handheld dermoscopy compared to SDD. Our results confirm that periodical dermoscopic examination enables the diagnosis of cutaneous melanoma at an earlier stage compared to first-time examination as this was associated in our patients with better prognostic features. However, in our long-term monitoring of low-risk subjects, Breslow tumor thickness and pT stage distribution did not differ between handheld periodical dermoscopy and SDD.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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