Evidence map›Paper›PMID 42819918›Full record

ArticleFrontiers in medicine2026

Artificial intelligence for rapid on-site evaluation of lymph node fine-needle aspiration: improving diagnostic efficiency and accuracy.

Chengcheng Du, Chunhai Li, Hong Meng, Fanlei Kong

Abstract read
In one paragraph

Article in Frontiers in medicine, 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

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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

4 authors.

Chengcheng DuDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.
Chunhai LiDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.
Hong MengDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.
Fanlei KongDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lymphadenopathy may result from inflammation, tuberculosis, or tumors, with lymph node status being a key prognostic indicator. Early accurate differentiation of benign and malignant lesions is therefore vital for clinical management. Although imaging offers adjunctive information, histopathology and cytology on biopsy specimens remain the gold standard, albeit with a 2-4 day turnaround. CT-guided biopsy ensures precise sampling, but final diagnosis depends on pathology. AI-ROSE is an emerging real-time cytological tool that can rapidly classify lesions and guide sampling/treatment decisions. While well-validated in lung biopsy, its role in lymph node biopsy is less studied, as most AI research emphasizes imaging over cytology. Therefore, this study assessed the clinical value and diagnostic concordance of AI-ROSE, providing a reference for intraoperative rapid diagnosis and specimen adequacy evaluation. Methods: This study included 54 patients who underwent lymph node biopsy from June 2024 to June 2026. All samples were obtained by percutaneous puncture under CT guidance and simultaneously underwent AI-ROSE analysis, exfoliative cytology examination, and histopathological examination. Using the histopathological results as the gold standard, the sensitivity, specificity, positive/negative predictive values, and accuracy of AI-ROSE and exfoliative cytology methods were calculated separately, and the consistency between the methods and histopathological diagnosis was analyzed. Results: The sensitivity of the AI-ROSE diagnosis was 90.48% (95% CI: 77.9% - 96.2%), and the diagnostic accuracy was 89.80% (95% CI: 78.2% - 95.6%). Both of these indicators were higher than those of the exfoliative cytology examination. The consistency between AI-ROSE and the pathological gold standard was moderate ( Conclusion: In this study, AI-ROSE showed higher sensitivity and diagnostic accuracy than traditional exfoliative cytology for lymph node biopsy. As a practical adjunctive tool, it offers real-time guidance on specimen adequacy and the need for repeat puncture, thereby streamlining the diagnostic process. Notably, AI-ROSE findings should be used as supplementary references and must not replace final histopathological diagnosis.

Indexed as

artificial intelligencebiopsylymph noterapid on-site evaluation (ROSE)tumor

Identifiers

PMID42819918
PMCPMC13625273

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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.