Evidence map›Paper›PMID 41074872›Full record

Observational studyEuropean journal of haematology2026

Core Needle Biopsies in Patients With Lymphoproliferative Malignancies: An Observational Single-Center Cohort Study.

Blas Holger Mogensen, Torsten Holm Nielsen, Mette Ølgod Pedersen, Lise Mette Rahbek Gjerdrum, Tarec Christoffer El-Galaly, Lars Møller Pedersen

Abstract readObservational Study
In one paragraph

Observational study in European journal of haematology, 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

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

1 citing paper in PubMed.

  1. Observational
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

6 authors.

Blas Holger MogensenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Torsten Holm NielsenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Mette Ølgod PedersenDepartment of Pathology, Zealand University Hospital, Roskilde, Denmark.
Lise Mette Rahbek GjerdrumDepartment of Pathology, Zealand University Hospital, Roskilde, Denmark.
Tarec Christoffer El-GalalyDepartment of Hematology, Aarhus University Hospital, Aarhus, Denmark.
Lars Møller PedersenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID https://orcid.org/0000-0002-9419-8841

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the diagnostic evaluation of suspected lymphoma, both core needle biopsy (CNB) and surgical excisional biopsy (SEB) are routinely employed for tissue sampling. While SEB remains the gold standard, CNB is a less invasive and more cost-effective alternative. However, concerns persist regarding its diagnostic yield. This study aimed to assess the diagnostic performance of CNB in comparison to SEB in routine clinical practice. We included 179 patients with newly diagnosed lymphoma referred to Zealand University Hospital in 2023, of whom 84 underwent CNB based on PET/CT findings. A definitive lymphoma diagnosis was established in 74% of CNB cases, compared to 98% with SEB, underscoring a lower diagnostic yield of CNB. The diagnostic accuracy of CNB varied by biopsy location, lymphoma subtype, and the volume of tissue obtained. Inconclusive diagnoses were more frequent in indolent lymphoma subtypes, biopsies yielding a limited number of tissue cylinders, and samples taken from the axillary and inguinal regions or extranodal sites. Grade 3-4 complications were observed in 1% of CNBs and in 5% of SEBs. Although CNB was a safe procedure, further refinement of biopsy techniques and improved patient selection are needed to enhance its diagnostic accuracy and clinical utility.

Indexed as

Lymphoproliferative DisordersAdultAgedAged, 80 and overBiopsy, Large-Core NeedleFemaleHumansLymphomaMaleMiddle AgedPositron Emission Tomography Computed TomographyYoung Adultcore needle biopsylymphomasurgical excision biopsy

Identifiers

PMID41074872
PMCPMC12673351

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Registered trials

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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.