Evidence map›Paper›PMID 42190192›Full record

ArticleDermatology practical & conceptual2026

Clinical and Dermoscopic Characterization of Mixed-Type Basal Cell Carcinoma.

Fethi Zaid, Kerem Balan, Gonca Elçin, Özay Gokoz, Duygu Gülseren

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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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fethi ZaidDepartment of Dermatology and Venereology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Kerem BalanDepartment of Dermatology and Venereology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Gonca ElçinDepartment of Dermatology and Venereology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Özay GokozDepartment of Medical Pathology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Duygu GülserenDepartment of Dermatology and Venereology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBasal cell carcinoma (BCC) is a malignant skin tumor that originates from epidermal basal cells or the outer root sheath of hair follicles. Identifying histopathological subtypes is crucial to guiding treatment and patient follow-up. While dermoscopic features associated with histopathological subtypes have been studied, the changes in dermoscopic findings in mixed-type BCC remain unclear.

objectivesThis study aimed to analyze the demographic characteristics of patients diagnosed with single and mixed-type BCC and to investigate the correlation between clinical and dermoscopic findings and histopathological subtypes.

resultsA total of 186 BCC lesions from 157 patients were analyzed. The mean patient age was 68.8±12.7 years (range: 30-94). The most common lesion location was the head and neck region (74.7%). The distribution of histopathological subtypes was as follows: nodular (42.5%), mixed-type (37.6%), superficial (12.4%), basosquamous (3.2%), infiltrative (2.7%), micronodular (1.1%), and fibroepithelial (0.5%). The most frequent mixed-type BCC combinations were nodular-infiltrative (32.9%), nodular-superficial (31.4%), and nodular-micronodular (12.9%).Short fine telangiectasia, yellow-white structureless areas, scales, and rosette structures were more frequent in mixed-type BCC. Corkscrew vessel patterns were more common in single-type lesions. The presence of a superficial component in mixed-type BCC was associated with wheel-like structures, while infiltrative components correlated with dotted and glomerular vessel patterns, and basosquamous components were linked to arborizing vessel patterns. Additionally, arborizing vessel patterns (P=0.019) and dotted vessel patterns (P=0.025) were associated with high-risk subtypes in mixed-type BCC.

conclusionOur study suggests that dermoscopic findings may serve as a guide to recognizing mixed-type BCC lesions, distinguishing between subtype components, and assisting in treatment decision-making based on these observations.

Identifiers

PMID42190192
PMCPMC13211923

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