The presence of eccentric hyperpigmentation should raise the suspicion of melanoma.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 03 02 2020
revised: 04 04 2020
accepted: 21 04 2020
pubmed: 14 5 2020
medline: 15 5 2021
entrez: 14 5 2020
Statut: ppublish

Résumé

Melanocytic lesions with eccentric hyperpigmentation (EH), even though without other dermatoscopic features of melanoma, are often excised. Aiming to understand whether the EH in a pigmented lesion is an accurate criterion of malignancy, we evaluated the capability of two evaluators, with different expertise, to correctly diagnose a melanoma when analysing a given lesion in toto versus a partial analysis, with only the EH or the non-hyperpigmented portion (non-EH) visible. Dermatoscopic images of 240 lesions (107 melanomas and 133 nevi) typified by EH were selected. Facial, acral, mucosal lesions and lesions showing clear-cut features of melanoma (except for atypical network) were excluded. Clinical and dermoscopic features (main pattern and numbers of colours) were described for all cases. Each image was split in two through a software so that only the EH or the non-EH was visible. Two blinded evaluators examined three sets of images, two with customized images and one with the non-modified ones: they were asked to give a dichotomous diagnosis (melanoma or nevus) for each image. Melanomas were significantly more frequently typified by colour variegation (3 colours in 44.8% and 4 colours in 41.1% of cases) and atypical network (88.1% in the EH). No significant differences in diagnostic accuracy emerged between the two evaluators. Sensitivity improved in the evaluation of the whole lesions (mean sensitivity 89.7%) in comparison with the evaluation of EH or non-EH alone (72.7-62.6%). Specificity increased when evaluating the EH (54.1%). Positive predictive value (PPV) and likelihood ratio (LR+) of EH resulted 52.3% and 1.4, meaning that in one case out of two with EH is a melanoma. Lesions with EH are challenging, regardless of dermoscopic experience. The EH is a robust criterion for malignancy, since the evaluation of the whole lesion, through an intralesional comparative approach, increases sensitivity.

Sections du résumé

BACKGROUND BACKGROUND
Melanocytic lesions with eccentric hyperpigmentation (EH), even though without other dermatoscopic features of melanoma, are often excised.
OBJECTIVE OBJECTIVE
Aiming to understand whether the EH in a pigmented lesion is an accurate criterion of malignancy, we evaluated the capability of two evaluators, with different expertise, to correctly diagnose a melanoma when analysing a given lesion in toto versus a partial analysis, with only the EH or the non-hyperpigmented portion (non-EH) visible.
METHODS METHODS
Dermatoscopic images of 240 lesions (107 melanomas and 133 nevi) typified by EH were selected. Facial, acral, mucosal lesions and lesions showing clear-cut features of melanoma (except for atypical network) were excluded. Clinical and dermoscopic features (main pattern and numbers of colours) were described for all cases. Each image was split in two through a software so that only the EH or the non-EH was visible. Two blinded evaluators examined three sets of images, two with customized images and one with the non-modified ones: they were asked to give a dichotomous diagnosis (melanoma or nevus) for each image.
RESULTS RESULTS
Melanomas were significantly more frequently typified by colour variegation (3 colours in 44.8% and 4 colours in 41.1% of cases) and atypical network (88.1% in the EH). No significant differences in diagnostic accuracy emerged between the two evaluators. Sensitivity improved in the evaluation of the whole lesions (mean sensitivity 89.7%) in comparison with the evaluation of EH or non-EH alone (72.7-62.6%). Specificity increased when evaluating the EH (54.1%). Positive predictive value (PPV) and likelihood ratio (LR+) of EH resulted 52.3% and 1.4, meaning that in one case out of two with EH is a melanoma.
CONCLUSIONS CONCLUSIONS
Lesions with EH are challenging, regardless of dermoscopic experience. The EH is a robust criterion for malignancy, since the evaluation of the whole lesion, through an intralesional comparative approach, increases sensitivity.

Identifiants

pubmed: 32402129
doi: 10.1111/jdv.16604
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2802-2808

Informations de copyright

© 2020 European Academy of Dermatology and Venereology.

Références

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Fikrle T, Pizinger K. Dermatoscopic differences between atypical melanocytic naevi and thin malignant melanomas. Melanoma Res 2006; 16: 45-50.
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Hofman-Wellenhof R, Blum A, Wolf I et al. Dermoscopic classification of atypical melanocytic nevi (Clark nevi). Arch Dermatol 2001; 137: 1575-1580.
Argenziano G, Catricalà C, Ardigo M et al. Seven-point checklist of dermoscopy revisited. Br J Dermatol 2011; 164: 785-790.
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Auteurs

S Borsari (S)

Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, Italy.

F Peccerillo (F)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

R Pampena (R)

Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, Italy.

M Lai (M)

Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

M Spadafora (M)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

E Moscarella (E)

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

A Lallas (A)

First Department of Dermatology, Aristotle University, Thessaloniki, Greece.

M A Pizzichetta (MA)

Department of Dermatology, University Hospital of Trieste, Trieste, Italy.
Division of Medical Oncology - Preventive Oncology, National Cancer Institute, Aviano, Italy.

I Zalaudek (I)

Department of Dermatology, University Hospital of Trieste, Trieste, Italy.

L Del Regno (L)

Institute of Dermatology, Catholic University of Rome and Fondazione Policlinico Universitario A. Gemelli, Rome, Italy.

K Peris (K)

Institute of Dermatology, Catholic University of Rome and Fondazione Policlinico Universitario A. Gemelli, Rome, Italy.

G Pellacani (G)

Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

C Longo (C)

Centro Oncologico ad Alta Tecnologia Diagnostica, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.

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