Evidence map›Paper›PMID 35509579›Full record

ArticleSurgical neurology international2022

Tumefactive multiple sclerosis versus high grade glioma: A diagnostic dilemma.

Heath French, Ariadna Fontes-Villalba, Monish Maharaj, Catherine Soo Yee Naidoo, Kartik Bhatia, Amanda Paterson, Raymond Cook, John Parratt

Open access · hybridAbstract read
In one paragraph

Article in Surgical neurology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

8 authors at 4 institutions in 4 countries.

Heath FrenchDepartments of Neurosurgery, Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
Ariadna Fontes-VillalbaNeurology, Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
Monish MaharajDepartment of Neurosurgery, Waikato Hospital, Hamilton, New Zealand.
Catherine Soo Yee NaidooDepartment of Radiology, Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
Kartik BhatiaDepartment of Radiology, Children's Hospital, Westmead.
Amanda PatersonDepartment of Neurosurgery, John Hunter Hospital, New Lambton Heights, New South Wales, Australia.
Raymond CookDepartments of Neurosurgery, Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
John ParrattNeurology, Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
Royal North Shore Hospital · AUChildren's Hospital at Westmead · AUWaikato Hospital · NZWestmead Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tumefactive demyelinating lesions (TDL) share similar clinical features and magnetic resonance imaging (MRI) characteristics with high grade glioma (HGG). This study develops an approach to navigating this diagnostic dilemma, with significant treatment implications as the management of both entities is drastically different. Methods: A retrospective analysis of 41 TDLs and 91 HGG with respect to demographics, presentation and classical MRI characteristics was performed. A diagnostic pathway was then developed to help diagnose TDLs based on whole neuraxis MRI and cerebrospinal fluid (CSF) examination. Results: The diagnosis of TDL is more likely than HGG in younger females who present with subacute or chronic symptoms. MRI characteristics favoring TDL over HGG include smaller size, open rim enhancement, little or no associated edema or mass effect and the presence of a T2 hypointense rim. MRI of the whole neuraxis for detection of other lesions typical of multiple sclerosis (MS), in combination with a lumbar puncture (LP) showing positive CSF-specific oligoclonal bands (OCB), was positive in 90% of the TDL cohort. Conclusion: The diagnostic pathway, proposed on the basis of specific clinicoradiological features, should be followed in patients with suspected TDL. If MRI demonstrates other lesions typical of MS and LP demonstrates positive CSF-specific OCBs, then patients should undergo a short course of IV steroids to look for clinical improvement. Patients, who continue to deteriorate, do not demonstrate other lesions on MRI or where the LP is negative for CSF-specific OCB, should be considered for biopsy if safe to do so. This pathway will give the patients the best chance at neurological preservation.

Indexed as

BiopsyDiagnostic dilemmaDiagnostic pathwayHigh grade gliomaTumefactive demyelinating lesionTumefactive multiple sclerosis

Identifiers

PMID35509579
PMCPMC9062904
OpenAlexW4226086449

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.