Volume 32, Issue 8 pp. 1263-1271
Original Article

Dermoscopic features and patterns of poromas: a multicentre observational case–control study conducted by the International Dermoscopy Society

M.A. Marchetti

M.A. Marchetti

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

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M.L. Marino

M.L. Marino

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

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P. Virmani

P. Virmani

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

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S.W. Dusza

S.W. Dusza

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

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A.A. Marghoob

A.A. Marghoob

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

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G. Nazzaro

G. Nazzaro

Department of Physiopathology and Transplantation, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy

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A. Lallas

A. Lallas

First Department of Dermatology, Aristotle University, Thessaloniki, Greece

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C. Landi

C. Landi

Dermatologic Unit, Surgical Department, “Infermi” Hospital, Rimini, Italy

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H. Cabo

H. Cabo

Dermatology Section, Medical Research Institute, University of Buenos Aires, Buenos Aires, Argentina

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R. Quiñones

R. Quiñones

Instituto Dermatologico de Jalisco, Guadalajara, Jal, Mexico

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E. Gomez

E. Gomez

Dermatology Center “Dr Ladislao de la Pascua”, Mexico City, Mexico

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S. Puig

S. Puig

Melanoma Unit, Department of Dermatology, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), University of Barcelona, Barcelona, Spain

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C. Carrera

Corresponding Author

C. Carrera

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

Melanoma Unit, Department of Dermatology, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), University of Barcelona, Barcelona, Spain

Correspondence: C. Carrera. E-mail: [email protected]Search for more papers by this author
First published: 01 December 2017
Citations: 34

Conflicts of interest:

None declared.

Funding sources:

This research was funded in part through the NIH/NCI Cancer Center Support Grant P30 CA008748.

Statement on prior presentation: Preliminary data of this study were presented as an oral presentation at the annual meeting of the American Academy of Dermatology on Friday, 3 March 2017.

Abstract

Background

Poromas are benign cutaneous sweat gland tumours that are challenging to identify. The dermoscopic features of poromas are not well characterized.

Objective

To determine the clinical-dermoscopic features of poromas.

Methods

Cross-sectional, observational study of 113 poromas and 106 matched control lesions from 16 contributors and eight countries. Blinded reviewers evaluated the clinical and dermoscopic features present in each clinical and dermoscopic image.

Results

Poromas were most commonly non-pigmented (85.8%), papules (35.4%) and located on non-acral sites (65.5%). In multivariate analysis, dermoscopic features associated with poroma included white interlacing areas around vessels (OR: 7.9, 95% CI: 1.9–32.5, P = 0.004), yellow structureless areas (OR: 2.5, 95% CI: 1.1–6.0, P = 0.04), milky-red globules (OR: 3.9, 95% CI: 1.4–11.1, P = 0.01) and poorly visualized vessels (OR: 33.3, 95% CI: 1.9–586.5, P = 0.02). The presence of branched vessels with rounded endings was positively associated with poromas but did not reach statistical significance (OR: 2.4, 95% CI: 0.8–6.5, P = 0.10). The presence of any of these five features was associated with a sensitivity and specificity of 62.8% and 82.0%, respectively.

Conclusion

We identified dermoscopic features that are specific to the diagnosis of poroma. Overall, however, the prevalence of these features was low. Significant clinical and dermoscopic variability is a hallmark of these uncommon tumours, which are most prevalent on non-acral sites.

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