Evidence map›Paper›PMID 42116633›Full record

ArticlePathology international2026

Standardized Instance-Level Quantification of CD34-Positive Vessels in Lymph Node Whole-Slide Images Using U-Net.

Satomi Omotani, Natsumi Yonemoto, Akifumi Muramoto, Motohiro Kobayashi

Abstract read
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Satomi OmotaniDepartment of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Fukui, Japan.
Natsumi YonemotoDepartment of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Fukui, Japan.
Akifumi MuramotoDepartment of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Fukui, Japan.
Motohiro KobayashiDepartment of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Fukui, Japan.ORCID https://orcid.org/0000-0002-7607-0801

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep learning enhances quantitative analysis of blood vessels in whole-slide images (WSIs), leading to precise and reliable counting. However, counting vessels in lymph nodes-which contain distinctive high endothelial venules (HEVs)-has not been systematically evaluated. Artificial intelligence (AI) approaches to vessel-counting fall into two categories: semantic segmentation, which provides a continuous mask, and instance segmentation, which treats each vessel as a separate object; prior work has emphasized the former. To address this gap, we adopted an instance-level approach to detect and count individual vessels. We developed a convolutional neural network (CNN) to quantify CD34-positive vessels in lymph-node WSIs, using U-Net, a widely used biomedical segmentation architecture. The model was trained over 4.0 million (4.0 M) iterations, followed by a fixed post-processing procedure to extract vessel instances. At 3.0 M, the model most faithfully captured CD34-positive vascular morphology. In the validation set, this checkpoint showed the highest morphological similarity. Furthermore, detection performance was robust with minimal variation across lymph nodes and training checkpoints. Using a simple fixed procedure, our method achieves accurate vessel detection and counting in lymph-node WSIs. This model provides a practical basis for standardized quantification and for studying lymph-node vascular morphology across normal, inflammatory, and lymphomatous states.

Indexed as

Antigens, CD34Image Processing, Computer-AssistedLymph NodesConvolutional Neural NetworksDeep LearningHumansAntigens, CD34AICD34deep learninglymph nodesvessels

Identifiers

PMID42116633
PMCPMC13161731

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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.