Evidence map›Paper›PMID 42351922›Full record

ArticleBioengineering (Basel, Switzerland)2026

A Unified Framework for Classification and Segmentation of Ambiguous Dual-Type Lesions in Colonoscopic Images.

Siqi Chen, Kun Jiang, Ruishi Lin, Xiufeng Su, Liyong Ma

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Siqi ChenDepartment of Control Science and Engineering, Harbin Institute of Technology, Harbin 150001, China.
Kun JiangWeihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai 264299, China.
Ruishi LinSchool of Information Science and Engineering, Harbin Institute of Technology, Weihai 264209, China.
Xiufeng SuWeihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai 264299, China.
Liyong MaDepartment of Control Science and Engineering, Harbin Institute of Technology, Harbin 150001, China.ORCID 0000-0002-0718-379X

Funding

National Key R&D Program of China 2024YFC2417403
6 · The paper itself

Abstract

Accurate analysis of lesions in colonoscopic images is essential for computer-aided diagnosis. However, most existing methods are designed for single-lesion segmentation and assume a predefined lesion category, limiting their applicability in real-world scenarios where multiple lesion types exhibit similar visual characteristics. To address this issue, we propose a unified framework for the joint classification and segmentation of dual-type lesions in colonoscopic images, enabling simultaneous identification and localization of submucosal lesions and polyps/adenomas. The proposed method integrates joint supervision, context-aware feature enhancement, and ambiguity-aware optimization to improve consistency between semantic recognition and spatial delineation. In particular, a soft-label supervision strategy is introduced to alleviate semantic ambiguity, while an imbalance-aware loss design enhances segmentation accuracy and reduces false negative predictions. Extensive experiments on both private and public datasets demonstrate that the proposed method achieves superior performance compared with representative CNN- and transformer-based approaches. Notably, the method shows clear advantages in segmentation accuracy, localization precision, and robustness under challenging conditions. Ablation studies further confirm the effectiveness of each component in the proposed framework. These results indicate that the proposed approach provides an effective solution for dual-type lesion analysis and has the potential to assist clinical decision-making in gastrointestinal endoscopy.

Indexed as

colonoscopic imagescomputer-aided diagnosisdeep learningdual-type lesionsjoint classification and segmentationsemantic ambiguity

Identifiers

PMID42351922
PMCPMC13295307

What OpenQuestion holds

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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.