Evidence map›Paper›PMID 40281781›Full record

ArticleBioengineering (Basel, Switzerland)2025

DermViT: Diagnosis-Guided Vision Transformer for Robust and Efficient Skin Lesion Classification.

Xuejun Zhang, Yehui Liu, Ganxin Ouyang, Wenkang Chen, Aobo Xu, Takeshi Hara, Xiangrong Zhou, Dongbo Wu

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Xuejun ZhangSchool of Computer, Electronics and Information, Guangxi University, Nanning 530004, China.ORCID 0000-0001-7689-4686
Yehui LiuSchool of Computer, Electronics and Information, Guangxi University, Nanning 530004, China.ORCID 0009-0000-2013-1700
Ganxin OuyangDepartment of Electrical, Electronic and Computer Engineering, Gifu University, Gifu 501-1193, Japan.
Wenkang ChenSchool of Computer, Electronics and Information, Guangxi University, Nanning 530004, China.
Aobo XuSchool of Computer, Electronics and Information, Guangxi University, Nanning 530004, China.
Takeshi HaraDepartment of Electrical, Electronic and Computer Engineering, Gifu University, Gifu 501-1193, Japan.
Xiangrong ZhouDepartment of Electrical, Electronic and Computer Engineering, Gifu University, Gifu 501-1193, Japan.ORCID 0000-0002-5838-5885
Dongbo WuDepartment of General Surgery, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou 545000, China.ORCID 0009-0000-4761-7452

Funding

Central guidance for local science and technology devel-opment funds projects No. 202201002Guangxi Zhuang Autonomous Region Health Commission Nos. Z-B20231432 and Z20210069Liuzhou Science and Technology Plan No. 2022SB019
6 · The paper itself

Abstract

Early diagnosis of skin cancer can significantly improve patient survival. Currently, skin lesion classification faces challenges such as lesion-background semantic entanglement, high intra-class variability, artifactual interference, and more, while existing classification models lack modeling of physicians' diagnostic paradigms. To this end, we propose DermViT, a medically driven deep learning architecture that addresses the above issues through a medically-inspired modular design. DermViT consists of three main modules: (1) Dermoscopic Context Pyramid (DCP), which mimics the multi-scale observation process of pathological diagnosis to adapt to the high intraclass variability of lesions such as melanoma, then extract stable and consistent data at different scales; (2) Dermoscopic Hierarchical Attention (DHA), which can reduce computational complexity while realizing intelligent focusing on lesion areas through a coarse screening-fine inspection mechanism; (3). Dermoscopic Feature Gate (DFG), which simulates the observation-verification operation of doctors through a convolutional gating mechanism and effectively suppresses semantic leakage of artifact regions. Our experimental results show that DermViT significantly outperforms existing methods in terms of classification accuracy (86.12%, a 7.8% improvement over ViT-Base) and number of parameters (40% less than ViT-Base) on the ISIC2018 and ISIC2019 datasets. Our visualization results further validate DermViT's ability to locate lesions under interference conditions. By introducing a modular design that mimics a physician's observation mode, DermViT achieves more logical feature extraction and decision-making processes for medical diagnosis, providing an efficient and reliable solution for dermoscopic image analysis.

Indexed as

dermoscopic image analysisskin cancerskin lesion classificationtransformer

Identifiers

PMID40281781
PMCPMC12025110

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.