Evidence map›Paper›PMID 28213912›Full record

ArticleBrain pathology (Zurich, Switzerland)2018

Diagnostic red flags: steroid-treated malignant CNS lymphoma mimicking autoimmune inflammatory demyelination.

Alonso Barrantes-Freer, Aylin Sophie Engel, Odir Antonio Rodríguez-Villagra, Anne Winkler, Markus Bergmann, Christian Mawrin, Tania Kuempfel, Hannah Pellkofer, Imke Metz, Annalen Bleckmann and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

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  6. Multiple sclerosis: a practical review for pathologists.Journal of pathology and translational medicine · 2025
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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

22 authors at 11 institutions in 4 countries.

Alonso Barrantes-FreerInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0001-9988-4667
Aylin Sophie EngelInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Odir Antonio Rodríguez-VillagraNeuroscience Research Center, University of Costa Rica, San José, Costa Rica.
Anne WinklerInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Markus BergmannInstitute of Neuropathology, Hospital Bremen Mitte, Bremen, Germany.
Christian MawrinInstitute of Neuropathology, University Hospital Magdeburg, Magdeburg, Germany.
Tania KuempfelInstitute of Clinical Neuroimmunology, Ludwig-Maximilians-University, Munich, Germany.
Hannah PellkoferInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Imke MetzInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Annalen BleckmannDepartment of Haematology-Oncology, University Medical Center Göttingen, Göttingen, Germany, University Medical Center Göttingen, Göttingen, Germany.
Silvia Hernández-DuránDepartment of Neurosurgery, University Medical Center Göttingen, Göttingen, Germany.
Sven SchipplingClinic for Neurology, University Hospital Zürich, Zürich, Switzerland.
Elisabeth J RushingInstitute of Neuropathology, University Hospital Zürich, Zürich, Switzerland.
Stephan FrankInstitute of Neuropathology, University Hospital Basel, Basel, Switzerland.
Markus GlatzelInstitute of Neuropathology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Jakob MatschkeInstitute of Neuropathology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Christian HartmannDepartment of Neuropathology, Institute of Pathology, University Medical Center Hannover, Hannover, Germany.
Guido ReifenbergerInstitute of Neuropathology, Heinrich Heine University, Düsseldorf, Germany.
Wolf MüllerDepartment of Neuropathology, University Medical Center Leipzig, Leipzig, Germany.
Hans-Ulrich SchildhausInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Wolfgang BrückInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Christine StadelmannInstitute of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Universitätsmedizin Göttingen · DEUniversität Hamburg · DEUniversity Hospital of Zurich · CHHeinrich Heine University Düsseldorf · DEInstitute of Neuroimmunology of the Slovak Academy of Sciences · SKKlinikum Bremen-Mitte · DEMedizinische Hochschule Hannover · DEUniversidad de Costa Rica · CRUniversity Hospital Leipzig · DEUniversity Hospital Magdeburg · DEUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of inflammation and demyelination in a central nervous system (CNS) biopsy points towards a limited, yet heterogeneous group of pathologies, of which multiple sclerosis (MS) represents one of the principal considerations. Inflammatory demyelination has also been reported in patients with clinically suspected primary central nervous system lymphoma (PCNSL), especially when steroids had been administered prior to biopsy acquisition. The histopathological changes induced by corticosteroid treatment can range from mild reduction to complete disappearance of lymphoma cells. It has been proposed that in the absence of neoplastic B cells, these biopsies are indistinguishable from MS, yet despite the clinical relevance, no histological studies have specifically compared the two entities. In this work, we analyzed CNS biopsies from eight patients with inflammatory demyelination in whom PCNSL was later histologically confirmed, and compared them with nine well defined early active multiple sclerosis lesions. In the patients with steroid-treated PCNSL (ST-PCNSL) the interval between first and second biopsy ranged from 3 to 32 weeks; all of the patients had received corticosteroids before the first, but not the second biopsy. ST-PCNSL patients were older than MS patients (mean age: ST-PCNSL: 62 ± 4 years, MS: 30 ± 2 years), and histological analysis revealed numerous apoptoses, patchy and incomplete rather than confluent and complete demyelination and a fuzzy lesion edge. The loss of Luxol fast blue histochemistry was more profound than that of myelin proteins in immunohistochemistry, and T cell infiltration in ST-PCNSL exceeded that in MS by around fivefold (P = 0.005). Our data indicate that in the presence of extensive inflammation and incomplete, inhomogeneous demyelination, the neuropathologist should refrain from primarily considering autoimmune inflammatory demyelination and, even in the absence of lymphoma cells, instigate close clinical follow-up of the patient to detect recurrent lymphoma.

Indexed as

Adrenal Cortex HormonesAgedAntineoplastic AgentsApoptosisBiopsyCentral Nervous System NeoplasmsCohort StudiesDiagnosis, DifferentialFemaleHumansImmunohistochemistryInflammationLymphomaMaleMiddle AgedMultiple SclerosisAdrenal Cortex HormonesAntineoplastic Agentscorticosteroidsdemyelinationdiffuse large B cell lymphomainflammationmultiple sclerosis

Identifiers

PMID28213912
PMCPMC8028373
OpenAlexW2588257494

What OpenQuestion holds

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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.