# Correlation of dermoscopic and histopathological features in basal cell carcinoma using computerized image analysis

**Authors:** Gökhan Kaya, Kübra Ataman, Sevgi Güleşçi, Ayşegül Yabaci Tak

PMC · DOI: 10.3389/fmed.2025.1581601 · Frontiers in Medicine · 2025-04-30

## TL;DR

This study uses computerized image analysis to explore how dermoscopic and histopathological features of basal cell carcinoma relate, aiming to improve diagnosis.

## Contribution

The novel use of AI-assisted image analysis to correlate dermoscopic pigmentation with tumor depth in BCC.

## Key findings

- Blue-gray ovoid nests and arborizing telangiectasias were common dermoscopic features in mixed-type BCC.
- Ulceration and multiple erosions were strongly linked to infiltrative BCC subtypes.
- A negative trend between pigmentation percentage and tumor depth was observed, though not statistically significant.

## Abstract

Basal cell carcinoma (BCC) is the most common skin cancer, exhibiting local invasiveness despite its low metastatic potential. Dermoscopy and histopathology are essential for diagnosis, while quantitative assessments may enhance lesion characterization.

This study aims to analyze the dermoscopic and histopathological characteristics of BCC and investigate the correlation between dermoscopic pigmentation patterns and tumor depth to improve lesion classification and diagnostic accuracy.

This retrospective study analyzed 41 patients with 42 histopathologically confirmed BCC lesions, evaluated at Nizip State Hospital and 25 Aralik State Hospital between April 2023 and February 2025. High-resolution dermoscopic images were analyzed alongside histopathological findings. AI-assisted computerized image analysis was employed to quantify lesion size and pigmentation percentage, while tumor depth and dermoscopic-histopathological correlations were manually assessed.

BCC was more prevalent in males (56.1%) and older adults, with a mean age of 67.1 years. The most commonly affected site was the nose (42.9%), followed by the cheek (14.3%) and upper lip (11.9%). Histopathologically, nodular (28.6%) and adenoid (28.6%) BCC were the most frequent subtypes. Dermoscopic analysis revealed blue-gray ovoid nests (57.14%) and arborizing telangiectasias (71.43%) as predominant features, particularly in mixed-type BCC, while blue-gray dots and globules (57.14%) were most common in micronodular BCC. Ulceration (45.24%) and multiple erosions (57.14%) were strongly associated with infiltrative BCC. A negative correlation was observed between pigmentation percentage and tumor depth, with deeper tumors exhibiting reduced pigmentation, though this trend was not statistically significant.

Comprehensive characterization of the dermoscopic and histopathological features of BCC enhances lesion differentiation. AI-assisted lesion size and pigmentation analysis, combined with histopathological evaluation, improves diagnostic precision. Further studies with larger cohorts are needed to validate these findings and refine classification criteria.

## Linked entities

- **Diseases:** basal cell carcinoma (MONDO:0005341)

## Full-text entities

- **Genes:** BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, PTGER4 (prostaglandin E receptor 4) [NCBI Gene 5734] {aka EP4, EP4R}
- **Diseases:** Fitzpatrick skin types II-IV (MESH:C000631847), skin cancer (MESH:D012878), adnexal neoplasms (MESH:D000292), xeroderma pigmentosum (MESH:D014983), epithelial tumor (MESH:D002277), Adenoid BCC (MESH:D002280), Ulceration (MESH:D014456), aggressiveness (MESH:D010554), melanocytic lesions (MESH:D009508), squamous cell carcinoma (MESH:D002294), bleeding (MESH:D006470), erosions (MESH:D014077), COVID-19 (MESH:D000086382), Pigmentation (MESH:D010859), telangiectasia (MESH:D013684), fibrosis (MESH:D005355), sweat gland carcinomas (MESH:D013544), basal cell nevus syndrome (MESH:D001478), scalp and extrafacial lesions (MESH:D004476), Tumors (MESH:D009369), malignant melanoma (MESH:D008545)
- **Chemicals:** paraffin (MESH:D010232), Hematoxylin (MESH:D006416), Hematoxylin and Eosin (-), H&amp;E (MESH:D006371), ozone (MESH:D010126), formalin (MESH:D005557), Eosin (MESH:D004801), ethanol (MESH:D000431), melanin (MESH:D008543), arsenic (MESH:D001151)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12074944/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12074944/full.md

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Source: https://tomesphere.com/paper/PMC12074944