Evidence map›Paper›PMID 42679968›Full record

ArticleJournal of vascular surgery. Venous and lymphatic disorders2026

Artificial intelligence-assisted identification of skin lesions associated with chronic venous insufficiency.

Ko Eun Kim, Jin Cheol Na, SangJun Song, Jiehyun Jeon, Seungjun Baek, Beom Suk Kim

Abstract read
In one paragraph

Article in Journal of vascular surgery. Venous and lymphatic disorders, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ko Eun KimDepartment of Dermatology, Korea University Guro Hospital, Seoul, Republic of Korea.
Jin Cheol NaDepartment of Computer Science and Engineering, Korea University, Seoul, Republic of Korea.
SangJun SongDepartment of Computer Science and Engineering, Korea University, Seoul, Republic of Korea.
Jiehyun JeonDepartment of Dermatology, Korea University Guro Hospital, Seoul, Republic of Korea.
Seungjun BaekDepartment of Computer Science and Engineering, Korea University, Seoul, Republic of Korea.
Beom Suk KimDepartment of Physical and Rehabilitation Medicine, Chung-Ang University College of Medicine, Seoul, Republic of Korea; Department of Physical and Rehabilitation Medicine, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong-si, Republic of Korea. Electronic address: mattkim9966@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to develop and validate a deep learning framework to classify chronic venous insufficiency (CVI)-related skin lesions and differentiate them from other lower-extremity dermatological conditions using dermoscopic images.

methodsWe retrospectively analyzed 677 high-resolution dermoscopic images from 248 patients, all histopathologically confirmed by skin biopsy. The dataset was categorized into three clinically distinct groups: (1) skin conditions related to CVI (eg, stasis dermatitis), (2) common inflammatory dermatological diseases, and (3) vasculitis. A Swin Transformer-based architecture (Microsoft Research)-a deep learning model that processes images at multiple spatial scales to capture both fine local detail and broader contextual patterns-was implemented to analyze dermoscopic images. A strict patient-level split was used to ensure model robustness, so that images from the same patient were never shared between training and test sets, which could otherwise artificially inflate performance estimates.

resultsThe proposed Swin Transformer model demonstrated superior diagnostic performance, achieving an overall area under the curve of 0.935 and classification accuracy of 0.848, significantly outperforming conventional convolutional neural networks and Vision Transformer baseline models. Group-specific area under the curve values were 0.942 for CVI-related conditions, 0.929 for inflammatory dermatoses, and 0.934 for vasculitis. Misclassifications were predominantly associated with overlapping dermoscopic features, such as purpuric patterns shared between stasis dermatitis and early-stage vasculitis. Notably, misclassification errors were directed more often toward the lower-risk pathway, with three CVI-related lesions misread as vasculitis, compared with only one vasculitis case misread as a CVI-related lesion.

conclusionsThis study demonstrates that a Swin Transformer-based deep learning model can effectively differentiate CVI-related skin lesions from inflammatory and vascular conditions, providing objective, noninvasive diagnostic support with the potential to streamline clinical workflows, facilitate early referrals to specialized care, and reduce reliance on invasive diagnostic procedures in the management of lower-extremity skin diseases.

Indexed as

Chronic venous diseaseChronic venous insufficiencyDeep learning algorithmPigmented purpuric dermatosisStasis dermatitis

Identifiers

PMID42679968
PMCPMC13634074

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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.