Evidence map›Paper›PMID 39777678›Full record

ArticleMuscle & nerve2025

Clinical and Electrophysiological Characteristics of 23 French Patients With Neurolymphomatosis.

Dylan Asmani, Jean-Baptiste Chanson, Céline Tard, Juliette Svahn, Antoine Pegat, Armelle Magot, Yann Péréon, Jean-Philippe Camdessanché, Samuel Naudin, Olivier Colin and 4 more

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Article in Muscle & nerve, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

14 authors.

Dylan AsmaniService de Neurologie, Centre de Référence Neuropathies Périphériques Rares, Centre Hospitalier Universitaire de Limoges, Limoges, France.
Jean-Baptiste ChansonCentre de Référence Des Maladies Neuromusculaires Nord/Est/Ile-de-France, Service de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Céline TardCentre de Reference des Maladies Rares Neuromusculaires Nord Est Ile-de-France Centre Constitutif de Lille, Lille, France.
Juliette SvahnService ENMG et de Pathologies Neuromusculaires, Centre de référence Des Maladies Neuromusculaires PACA-Réunion-Rhône Alpes, Hôpital Neurologique P. Wertheimer, Hospices Civils de Lyon, Bron, France.
Antoine PegatService ENMG et de Pathologies Neuromusculaires, Centre de référence Des Maladies Neuromusculaires PACA-Réunion-Rhône Alpes, Hôpital Neurologique P. Wertheimer, Hospices Civils de Lyon, Bron, France.ORCID https://orcid.org/0000-0003-1563-9432
Armelle MagotLaboratoire d'Explorations Fonctionnelles, Centre de Référence Maladies Neuromusculaires Rares AOC, Nantes, France.
Yann PéréonLaboratoire d'Explorations Fonctionnelles, Centre de Référence Maladies Neuromusculaires Rares AOC, Nantes, France.
Jean-Philippe CamdessanchéNeurology Department, University Hospital of Saint-Etienne, Saint-Etienne, France.
Samuel NaudinService de Neurologie, Centre Hospitalier de Brive-la-Gaillarde, Brive-la-Gaillarde, France.
Olivier ColinService de Neurologie, Centre Hospitalier de Brive-la-Gaillarde, Brive-la-Gaillarde, France.
Guillaume TaiebDepartment of Neurology, CHU Montpellier, Hôpital Gui de Chauliac, Montpellier, France.
Idrissa CoulibalyDepartment of Internal Medicine, Hospital Center of Cholet, Cholet, France.
Laurent MagyService de Neurologie, Centre de Référence Neuropathies Périphériques Rares, Centre Hospitalier Universitaire de Limoges, Limoges, France.
Simon FrachetService de Neurologie, Centre de Référence Neuropathies Périphériques Rares, Centre Hospitalier Universitaire de Limoges, Limoges, France.ORCID https://orcid.org/0000-0002-4685-0786

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

aimsNeurolymphomatosis is a hematological condition defined by the direct infiltration of malignant lymphomatous cells into the peripheral nervous system. Since nerve conduction studies may disclose demyelinating features, clinicians may misdiagnose neurolymphomatosis as chronic inflammatory demyelinating polyneuropathy (CIDP). This study aimed to determine whether patients with neurolymphomatosis met the 2021 revised criteria for CIDP.

methodsWe retrospectively analyzed 23 patients with primary or secondary neurolymphomatosis from nine French hospitals. We analyzed whether patients with a diagnosis of neurolymphomatosis met the 2010 and 2021 CIDP criteria.

results152 motor nerves were analyzed, and conduction blocks were found in 13.8% of them. Eight patients (34.7%) demonstrated at least one conduction block. Other demyelinating parameters fulfilling the 2021 CIDP criteria were rare, including reduced conduction velocities (1.7%), prolonged distal motor latencies (3%), absent F-waves (12.4%), and prolonged F-wave latencies (7.7%). Five patients met the 2010 CIDP criteria, whereas only one met the 2021 CIDP criteria. DISCUSSION: Demyelinating features are rare in neurolymphomatosis, and a conduction block is the most frequent abnormality. Consequently, only one patient met the 2021 criteria for CIDP diagnosis. This is likely attributable to the inclusion of sensory criteria. Furthermore, the new criteria emphasize the importance of identifying red flags, such as pain or monoclonal gammopathy, which could suggest an alternative diagnosis to CIDP. Clinicians should consider neurolymphomatosis in patients who present with red flags or atypical CIDP.

Indexed as

Neural ConductionNeurolymphomatosisPolyradiculoneuropathy, Chronic Inflammatory DemyelinatingAdultAgedAged, 80 and overFemaleFranceHumansMaleMiddle AgedRetrospective StudiesCIDPconduction blockdemyelinating parametersneurolymphomatosisneuropathy

Identifiers

PMID39777678
PMCPMC11887519

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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.