Analysis of dermoscopic changes of blue nevi on digital follow-up: A 21-year retrospective cohort study.


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:
May 2023
Historique:
received: 13 09 2022
accepted: 05 01 2023
medline: 17 4 2023
pubmed: 26 1 2023
entrez: 25 1 2023
Statut: ppublish

Résumé

Blue nevi are benign dermal melanocytic proliferations that are often easy to recognize clinically. Rarely, these lesions can display atypical features, suggesting the presence of a malignant blue nevus or mimicking cutaneous metastases of melanoma. To describe the clinical evolution of blue nevi over time and to assess the need for monitoring these lesions. We conducted a retrospective cohort study of 103 patients who were followed between December 1998 and November 2019. An artificial intelligence algorithm was used to identify blue nevi from the databases of two digital epiluminescence devices. Changes in the area of each lesion were calculated with a segmentation neural network. We included 123 blue nevi from 103 patients. Most of the lesions segmented, 99 (91.7%), were considered stable. Of the 9 (8.3%) growing blue nevi identified, 2 (1.85%) showed significant growth. The studied growing blue nevi turned out to be cellular blue nevi, presented with a low tumour mutation burden and GNAQ c.626A>T alteration was identified in both lesions. Some clinical variants of blue nevi might not be included. Most blue nevi remain stable during their evolution. Rarely, they can show progressive growth, although histopathological or molecular signs of malignancy have not been identified.

Sections du résumé

BACKGROUND BACKGROUND
Blue nevi are benign dermal melanocytic proliferations that are often easy to recognize clinically. Rarely, these lesions can display atypical features, suggesting the presence of a malignant blue nevus or mimicking cutaneous metastases of melanoma.
OBJECTIVE OBJECTIVE
To describe the clinical evolution of blue nevi over time and to assess the need for monitoring these lesions.
METHODS METHODS
We conducted a retrospective cohort study of 103 patients who were followed between December 1998 and November 2019. An artificial intelligence algorithm was used to identify blue nevi from the databases of two digital epiluminescence devices. Changes in the area of each lesion were calculated with a segmentation neural network.
RESULTS RESULTS
We included 123 blue nevi from 103 patients. Most of the lesions segmented, 99 (91.7%), were considered stable. Of the 9 (8.3%) growing blue nevi identified, 2 (1.85%) showed significant growth. The studied growing blue nevi turned out to be cellular blue nevi, presented with a low tumour mutation burden and GNAQ c.626A>T alteration was identified in both lesions.
LIMITATIONS CONCLUSIONS
Some clinical variants of blue nevi might not be included.
CONCLUSIONS CONCLUSIONS
Most blue nevi remain stable during their evolution. Rarely, they can show progressive growth, although histopathological or molecular signs of malignancy have not been identified.

Identifiants

pubmed: 36695073
doi: 10.1111/jdv.18915
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

914-921

Subventions

Organisme : Fondo de Investigaciones Sanitarias
ID : PI18/00419
Organisme : Fondo de Investigaciones Sanitarias
ID : PI18/01077
Organisme : Generalitat de Catalunya
ID : 2017/SGR1134
Organisme : CIBER de Enfermedades Raras of the Instituto de Salud Carlos III, Spain
Organisme : ISCIII-Subdireccion General de Evaluacion and European Regional Development Fund (ERDF)

Informations de copyright

© 2023 European Academy of Dermatology and Venereology.

Références

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Auteurs

Francesc Alamon-Reig (F)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.

Marc Combalia (M)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.

Raquel Albero-González (R)

Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Department of Pathology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.

Llúcia Alòs (L)

Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Department of Pathology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.

Cristina Carrera (C)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Centre of Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Joan Anton Puig-Butillé (JA)

Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Centre of Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Molecular Biology CORE Laboratory, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.

José Luis Villanueva-Cañas (JL)

Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Molecular Biology CORE Laboratory, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.

Susana Puig (S)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Centre of Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Josep Malvehy (J)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Centre of Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Sebastian Podlipnik (S)

Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.

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