Dermoscopic features of mammary Paget's disease: a retrospective case-control study by the International Dermoscopy Society.


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:
Oct 2019
Historique:
received: 05 03 2019
accepted: 17 05 2019
pubmed: 5 7 2019
medline: 12 3 2020
entrez: 5 7 2019
Statut: ppublish

Résumé

Mammary Paget's disease (MPD) is a rare intraepidermal adenocarcinoma of the nipple-areola complex, associated with an underlying breast cancer in approximately 90% of cases. Delayed diagnosis of MPD is common. Its dermoscopic features have been ill defined in the literature. To determine the clinical and dermoscopic features of MPD versus other dermatologic entities that involve nipple and areola. Members of the IDS were invited to submit any case of histologically confirmed MPD, as well as other benign and malignant dermatoses that involve the nipple and areola complex. A standardized evaluation of the dermoscopic images was performed and the results were statistically analyzed. Sixty-five lesions were included in the study, 22 (33.8%) of them MPD and 43 (66.2%) controls. The most frequent dermoscopic criteria of MPD were white scales (86.4%) and pink structureless areas (81.8%), followed by dotted vessels (72.7%), erosion/ulceration (68.2%) and white shiny lines (63.6%). The multivariate analysis showed that white scales and pink structureless areas were significant predictors of MPD, posing a 68-fold and a 31-fold probability of MPD, respectively. Split of the population into pigmented and non-pigmented lesions showed that in pigmented MPD, pink structureless areas, white lines and grey granules and dots are positive predictors of the disease. Among non-pigmented lesions, pink structureless areas, white lines, erosion/ulceration and white scales served as predictors of MPD. The most frequent profile of an individual with MPD is an elderly female with unilateral, asymptomatic, erythematous plaque of the nipple, dermoscopically displaying pink structureless areas, fine white scales, dotted and a few short linear vessels. In case of pigmentation we may also observe brown structureless areas and pigmented granules. Small sample size, retrospective design.

Sections du résumé

BACKGROUND BACKGROUND
Mammary Paget's disease (MPD) is a rare intraepidermal adenocarcinoma of the nipple-areola complex, associated with an underlying breast cancer in approximately 90% of cases. Delayed diagnosis of MPD is common. Its dermoscopic features have been ill defined in the literature.
OBJECTIVES OBJECTIVE
To determine the clinical and dermoscopic features of MPD versus other dermatologic entities that involve nipple and areola.
METHODS METHODS
Members of the IDS were invited to submit any case of histologically confirmed MPD, as well as other benign and malignant dermatoses that involve the nipple and areola complex. A standardized evaluation of the dermoscopic images was performed and the results were statistically analyzed.
RESULTS RESULTS
Sixty-five lesions were included in the study, 22 (33.8%) of them MPD and 43 (66.2%) controls. The most frequent dermoscopic criteria of MPD were white scales (86.4%) and pink structureless areas (81.8%), followed by dotted vessels (72.7%), erosion/ulceration (68.2%) and white shiny lines (63.6%). The multivariate analysis showed that white scales and pink structureless areas were significant predictors of MPD, posing a 68-fold and a 31-fold probability of MPD, respectively. Split of the population into pigmented and non-pigmented lesions showed that in pigmented MPD, pink structureless areas, white lines and grey granules and dots are positive predictors of the disease. Among non-pigmented lesions, pink structureless areas, white lines, erosion/ulceration and white scales served as predictors of MPD.
CONCLUSIONS CONCLUSIONS
The most frequent profile of an individual with MPD is an elderly female with unilateral, asymptomatic, erythematous plaque of the nipple, dermoscopically displaying pink structureless areas, fine white scales, dotted and a few short linear vessels. In case of pigmentation we may also observe brown structureless areas and pigmented granules.
LIMITATIONS CONCLUSIONS
Small sample size, retrospective design.

Identifiants

pubmed: 31270878
doi: 10.1111/jdv.15732
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1892-1898

Informations de copyright

© 2019 European Academy of Dermatology and Venereology.

Références

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Auteurs

Z Apalla (Z)

State Dermatology Department, Hippokratio General Hospital, Thessaloniki, Greece.

E Errichetti (E)

Institute of Dermatology, 'Santa Maria della Misericordia' University Hospital, Udine, Italy.

A Kyrgidis (A)

Department of Clinical Pharmacology, Aristotle University of Thessaloniki, Thessaloniki, Greece.

W Stolz (W)

Clinic of Dermatology II, Munich Hospital, Munich, Germany.

S Puig (S)

Department of Dermatology, Hospital Clinic, Barcelona, Spain.

J Malvehy (J)

Department of Dermatology, Hospital Clinic, Barcelona, Spain.

I Zalaudek (I)

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

E Moscarella (E)

Dermatology Unit, University of Campania, Naples, Italy.

C Longo (C)

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

A Blum (A)

Public, Private and Teaching Practice of Dermatology, Konstanz, Germany.

S Lanssens (S)

Dermatologie Maldegem, Maldegem, Belgium.

F Savoia (F)

Division of Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, S.Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

P Tschandl (P)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

H Kittler (H)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

C Sinz (C)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

G Stinco (G)

Institute of Dermatology, 'Santa Maria della Misericordia' University Hospital, Udine, Italy.

G Argenziano (G)

Dermatology Unit, University of Campania, Naples, Italy.

E Lazaridou (E)

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

A Lallas (A)

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

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