Evidence map›Paper›PMID 41957293›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

[

Nicolas Martinage, Julie Guyot, Gauthier Delaby, Damien Huglo, Emmanuel Ledoult, Clio Baillet

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 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. 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

6 authors.

Nicolas MartinageCentre Hospitalier Universitaire de Lille, Nuclear Medicine Department, Lille University Hospital, Lille, France. nicolas.martinage.etu@univ-lille.fr.ORCID 0009-0007-0647-3430
Julie GuyotInternal Medicine and Clinical Immunology Department, Huriez Hospital, Centre de Référence des Maladies Auto-Immunes Systémiques Rares du Nord, Lille University Hospital, Méditerranée et Guadeloupe (CeRAINOM), Nord-Ouest, Lille, France.
Gauthier DelabyCentre Hospitalier Universitaire de Lille, Nuclear Medicine Department, Lille University Hospital, Lille, France.
Damien HugloCentre Hospitalier Universitaire de Lille, Nuclear Medicine Department, Lille University Hospital, Lille, France.
Emmanuel LedoultInternal Medicine and Clinical Immunology Department, Huriez Hospital, Centre de Référence des Maladies Auto-Immunes Systémiques Rares du Nord, Lille University Hospital, Méditerranée et Guadeloupe (CeRAINOM), Nord-Ouest, Lille, France.
Clio BailletCentre Hospitalier Universitaire de Lille, Nuclear Medicine Department, Lille University Hospital, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePolyarteritis nodosa (PAN) is a rare necrotizing vasculitis of medium-sized vessels with heterogeneous presentations and a challenging diagnosis. While [18F]FDG PET/CT is established in large-vessel vasculitis, its role in PAN remains unclear. A distinctive “ant-farm” uptake pattern has recently been associated with PAN. This study assessed the diagnostic value of [18F]FDG PET/CT in PAN.

methodsPatients diagnosed with PAN who underwent [18F]FDG PET/CT between 2010 and 2025 were retrospectively included. Scans were blindly reviewed by two nuclear medicine physicians using a standardized grid. Abnormal uptakes, including the “ant-farm” pattern, were systematically recorded and correlated with clinical, biological, and histopathological data.

resultsForty-seven patients were included. Abnormal uptake was frequently found in the bone marrow (83%), lymph nodes (40%), and spleen (34%). Abnormal vascular uptake was observed in 36% of cases, predominantly in the femoral and tibial arteries. The “ant-farm” pattern was identified in 34% of patients with excellent inter-observer reproducibility (κ = 0.80). It was more frequent with recent PET/CT devices and whole-body acquisitions and was associated with higher C-reactive protein levels and fewer PAN-suggestive biopsies. Distinct uptake patterns were observed in etiologies of secondary PAN, including VEXAS syndrome.

conclusion[18F]FDG PET/CT is a valuable diagnostic tool in PAN and may also help identify secondary causes. The consistent “ant-farm” pattern may help distinguish patients with more inflammatory features, negative biopsy results and less PAN-related organ involvement.

Indexed as

Fluorodeoxyglucose F18Polyarteritis NodosaPositron Emission Tomography Computed TomographyAdultAgedFemaleHumansMaleMiddle AgedRadiopharmaceuticalsRetrospective StudiesFluorodeoxyglucose F18RadiopharmaceuticalsAnt-farmDiagnosisFDGPET/CTPolyarteritis nodosa

Identifiers

PMID41957293
PMCPMC13197267

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Registered trials

None linked

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.