Evidence map›Paper›PMID 30054790›Full record

ArticleJournal of neurology2018

Inaugural tumor-like multiple sclerosis: clinical presentation and medium-term outcome in 87 patients.

G Balloy, J Pelletier, L Suchet, C Lebrun, M Cohen, P Vermersch, H Zephir, E Duhin, O Gout, R Deschamps and 20 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

17 citing papers in PubMed, 48 citations in OpenAlex.

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  17. Tumefactive demyelination: Clinical outcomes, lesion evolution and treatments.Multiple sclerosis journal - experimental, translational and clinical
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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

30 authors at 11 institutions in 1 country.

G BalloyNeurology Department, University of Nantes Hospital, Nantes, France. gaelle.balloy@chu-nantes.fr.
J PelletierNeurosciences Unit, Neurology Department, Timone Hospital, Aix Marseille University, APHM, Marseille, France.
L SuchetNeurosciences Unit, Neurology Department, Timone Hospital, Aix Marseille University, APHM, Marseille, France.
C LebrunUniversity of Nice Hospital, Nice, France.
M CohenUniversity of Nice Hospital, Nice, France.
P VermerschUniversity of Lille Hospital, Lille, France.
H ZephirUniversity of Lille Hospital, Lille, France.
E DuhinUniversity of Lille Hospital, Lille, France.
O GoutRothschild Foundation, Paris, France.
R DeschampsRothschild Foundation, Paris, France.
E Le PageUniversity of Rennes Hospital, Rennes, France.
G EdanUniversity of Rennes Hospital, Rennes, France.
P LabaugeUniversity of Montpellier Hospital, Montpellier, France.
C Carra-DallieresUniversity of Montpellier Hospital, Montpellier, France.
L RumbachUniversity Besançon Hospital, Besançon, France.
E BergerUniversity Besançon Hospital, Besançon, France.
P LejeuneLa Roche sur Yon Hospital, La Roche-sur-Yon, France.
P DevosBoulogne-sur-Mer Hospital, Boulogne-sur-Mer, France.
J-B N'KendjuoDunkerque Hospital, Dunkerque, France.
M CoustansCornouaille Hospital, Quimper, France.
E Auffray-CalvierRadiology Department, University of Nantes Hospital, Nantes, France.
B Daumas-DuportRadiology Department, University of Nantes Hospital, Nantes, France.
L MichelNeurology Department, University of Nantes Hospital, Nantes, France.
F LefrereNeurology Department, University of Nantes Hospital, Nantes, France.
D A LaplaudNeurology Department, University of Nantes Hospital, Nantes, France.
C BrossetMilitary Hospital, Marseille, France.
P DerkinderenNeurology Department, University of Nantes Hospital, Nantes, France.
J de SezeUniversity of Strasbourg Hospital, Strasbourg, France.
S WiertlewskiNeurology Department, University of Nantes Hospital, Nantes, France.
Société Francophone de la Sclérose en Plaques
Nantes Université · FRUniversité de Lille · FRAix-Marseille Université · FRUniversité de Montpellier · FRCentre Hospitalier de Cornouaille · FRCentre Hospitalier Universitaire de Besançon · FRFondation de Rothschild · FRUniversité de Strasbourg · FRCentre Hospitalier Universitaire de Rennes · FRRoche (France) · FRUniversité d'été de Boulogne-sur-Mer · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumefactive demyelinating lesions of the central nervous system can be the initial presentation in various pathological entities [multiple sclerosis (the most common), Balo's concentric sclerosis, Schilder's disease and acute disseminated encephalomyelitis] with overlapping clinical presentation. The aim of our study was to better characterize these patients.

methodsEighty-seven patients (62 women and 25 men) from different MS centers in France were studied retrospectively. Inclusion criteria were (1) a first clinical event (2) MRI showing one or more large demyelinating lesions (20 mm or more in diameter) with mass-like features. Patients with a previous demyelinating event (i.e. confirmed multiple sclerosis) were excluded.

resultsMean age at onset was 26 years. The most common initial symptoms (67% of the patients) were hemiparesis or hemiplegia. Aphasia, headache and cognitive disturbances (i.e. atypical symptoms for demyelinating diseases) were observed in 15, 18 and 15% of patients, respectively. The mean largest diameter of the tumefactive lesions was 26.9 mm, with gadolinium enhancement in 66 patients (81%). Twenty-one patients (24%) had a single tumefactive lesion. During follow-up (median time 5.7 years) 4 patients died, 70 patients improved or remained stable and 12 worsened. 86% of patients received initial corticosteroid treatment, and 73% received disease-modifying therapy subsequently. EDSS at the end of the follow-up was 2.4 ± 2.6 (mean ± SD).

conclusionThis study provides further evidence that the clinical course of MS presenting with large focal tumor-like lesions does not differ from that of classical relapsing-remitting MS, once the noisy first relapsing occurred.

Indexed as

AdultBrainDiffuse Cerebral Sclerosis of SchilderDisease ProgressionFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMultiple SclerosisRetrospective StudiesBaloDemyelinating diseaseMultiple sclerosisPseudo-tumoral formSchilder

Identifiers

PMID30054790
OpenAlexW2884090025

What OpenQuestion holds

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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.