Evidence map›Paper›PMID 41912202›Full record

ArticleDermatology practical & conceptual2026

Dermoscopic Features of Pigmented Bowen Disease in Phototype IV Patients.

Gabriel Salerni, Horacio Cabo, Emilia N Cohen-Sabban, Sonia Rodríguez-Saa, Flavia Carolina Pozzobon, Cristian Navarrete-Dechent, Ivonne Arellano-Mendoza, Virginia M González, Renato Marchiori Bakos, Nicole Orendain and 5 more

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Article in Dermatology practical & conceptual, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

15 authors.

Gabriel SalerniDermatology Department, Hospital Provincial del Centenario de Rosario - Universidad Nacional de Rosario, Grupo Centro, Rosario, Argentina.
Horacio CaboMaster of Ibero-Latin American Dermatology (CILAD), Universidad de Buenos Aires, Argentina.
Emilia N Cohen-SabbanHead of Dermatology Service, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Argentina.
Sonia Rodríguez-SaaDepartment of Dermatology, Hospital El Carmen, Obra Social de Empleados Públicos (OSEP), Godoy Cruz, Mendoza, Argentina.
Flavia Carolina PozzobonCentro de Diagnostico Dermatológico, Bogotá, Colombia; Instituto Nacional de Cancerología, Bogotá, Colombia.
Cristian Navarrete-DechentMelanoma and Skin Cancer Unit, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Ivonne Arellano-MendozaDepartment of Dermatology and Dermatooncology, Hospital Dalinde, Ciudad de Mexico, Mexico.
Virginia M GonzálezDermatology Department, Hospital Alemán, Buenos Aires, Argentina.
Renato Marchiori BakosDepartment of Dermatology, Hospital de Clínicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Nicole OrendainPrivate practice, Guadalajara, Mexico.
Malynahi Tapia-JuarezPrivate practice, Ciudad de Mexico, Mexico.
Luis Morales GodinezUniversidad Autónoma de México. Private practice Ciudad de México, Mexico and Guatemala.
Diana Guerrero HernándezHospital General ISSSTE, Tacuba Ciudad de México, Universidad Nacional Autónoma de México.
Sofía AndreDepartment of Dermatology, Hospital Central, Mendoza, Argentina.
Susana PuigMelanoma Unit, Hospital Clinic Barcelona, University of Barcelona, Barcelona, Spain. CIBER de enfermedades raras, Instituto de Salud Carlos III, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionResearch on the dermoscopic features of pigmented Bowen disease (pBD) in individuals with phototype IV skin is limited and consists primarily of case reports or small studies.

objectivesWe sought to describe the clinical and dermoscopic characteristics of 21 cases of pBD in a skin phototype IV population.

methodsWe conducted a multicenter retrospective analysis of 21 histopathologically confirmed cases of pBD under the auspices of the Dermoscopy Chapter of the Ibero-Latin American College of Dermatology (CILAD).

resultsA total of 21 pBD cases in phototype IV patients (57% male, mean age 63.1 years) were analyzed. Lesions were most frequently located on the upper extremities and head and neck area (29% and 24%, respectively) and exhibited brown (90.5%) and pink (90.5%) coloration, with a higher prevalence of gray, black, and blue compared to lighter phototypes. Structureless areas (90.5%) and pigmented dots in a linear arrangement (71.4%) were the most frequent dermoscopic findings. Non-specific dermoscopic findings were observed in 23.8% (N=5) of cases.

conclusionPBD in phototype IV presents with a distinct dermoscopic pattern, including a higher proportion black and blue colors and fewer vascular structures than observed in lighter phototypes. The most prominent dermoscopic findings were structureless areas and pigmented dots, either in a central or peripheral linear arrangement; however, in a quarter of the cases, no specific clue was observed. These findings emphasize the need for tailored diagnostic approaches and the importance of biopsy when specific dermoscopic features are absent.

Identifiers

PMID41912202
PMCPMC12952806

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