Volume 173, Issue 1 pp. 106-114
Clinical and Laboratory Investigations

Pigmented nodular melanoma: the predictive value of dermoscopic features using multivariate analysis

M.A. Pizzichetta

Corresponding Author

M.A. Pizzichetta

Division of Medical Oncology – Preventive Oncology, Centro di Riferimento Oncologico, National Cancer Institute, Via Franco Gallini, 2, 33081 Aviano, Italy

Correspondence

Maria Antonietta Pizzichetta.

E-mail: [email protected]

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H. Kittler

H. Kittler

Department of Dermatology, University of Vienna, Vienna, Austria

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I. Stanganelli

I. Stanganelli

Skin Cancer Unit, Istituto Tumori Romagna (IRST), Meldola, Italy

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R. Bono

R. Bono

Istituto Dermopatico Immacolata, IRCCS, Rome, Italy

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S. Cavicchini

S. Cavicchini

Department of Dermatology, Fondazione Ospedale Maggiore Policlinico IRCCS, Milan, Italy

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V. De Giorgi

V. De Giorgi

Department of Dermatology, University of Florence, Florence, Italy

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G. Ghigliotti

G. Ghigliotti

Clinic of Dermatology, IRCCS San Martino – Ist, Genoa, Italy

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P. Quaglino

P. Quaglino

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

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P. Rubegni

P. Rubegni

Department of Dermatology, University of Siena, Siena, Italy

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G. Argenziano

G. Argenziano

Skin Cancer Unit, Arcispedale Santa Maria Nuova IRCCS, Reggio Emilia, Italy

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R. Talamini

R. Talamini

Unit of Epidemiology and Biostatistics, Centro di Riferimento Oncologico, National Cancer Institute, Via Franco Gallini, 2, 33081 Aviano, Italy

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for the Italian Melanoma Intergroup

the Italian Melanoma Intergroup

See Appendixfor the members of the Italian Melanoma Intergroup.Search for more papers by this author
First published: 27 April 2015
Citations: 30

Funding sources:

None.

Conflicts of interest:

None declared.

Summary

Background

Nodular melanoma (NM), representing 10–30% of all melanomas, plays a major role in global mortality related to melanoma. Nonetheless, the literature on dermoscopy of NM is scanty.

Objectives

To assess odds ratios (ORs) to quantify dermoscopic features of pigmented NM vs. pigmented superficial spreading melanoma (SSM), and pigmented nodular nonmelanocytic and benign melanocytic lesions.

Methods

To assess the presence or absence of global patterns and dermoscopic criteria, digitized images of 457 pigmented skin lesions from patients with a histopathological diagnosis of NM (= 75), SSM (= 93), and nodular nonmelanocytic and benign melanocytic lesions (= 289; namely, 39 basal cell carcinomas, 85 seborrhoeic keratoses, 81 blue naevi, and 84 compound/dermal naevi) were retrospectively collected and blindly evaluated by three observers.

Results

Multivariate analysis showed that ulceration (OR 4·07), homogeneous disorganized pattern (OR 10·76), and homogeneous blue pigmented structureless areas (OR 2·37) were significantly independent prognostic factors for NM vs. SSM. Multivariate analysis of dermoscopic features of NM vs. nonmelanocytic and benign melanocytic lesions showed that the positive correlating features leading to a significantly increased risk of NM were asymmetric pigmentation (OR 6·70), blue–black pigmented areas (OR 7·15), homogeneous disorganized pattern (OR 9·62), a combination of polymorphous vessels and milky-red globules/areas (OR 23·65), and polymorphous vessels combined with homogeneous red areas (OR 33·88).

Conclusions

Dermoscopy may be helpful in improving the recognition of pigmented NM by revealing asymmetric pigmentation, blue–black pigmented areas, homogeneous disorganized pattern and abnormal vascular structures, including polymorphous vessels, milky-red globules/areas and homogeneous red areas.

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