Evidence map›Paper›PMID 34128073›Full record

ArticleJournal of neuropathology and experimental neurology2021

Sarcomatous Meningioma: Diagnostic Pitfalls and the Utility of Molecular Testing.

Calixto-Hope G Lucas, Patrick Devine, David A Solomon, Caterina Giannini, Guido Reifenberger, Sonika Dahiya, Dario Caccamo, Arie Perry

Open access · greenAbstract readCase Reports
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Left dural-based mass in a 62-year-old female.Brain pathology (Zurich, Switzerland) · 2023
    Article
  6. Review
  7. 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

8 authors at 5 institutions in 2 countries.

Calixto-Hope G LucasDepartment of Pathology, San Francisco, California, USA.ORCID 0000-0002-8347-9592
Patrick DevineDepartment of Pathology, San Francisco, California, USA.
David A SolomonDepartment of Pathology, San Francisco, California, USA.
Caterina GianniniDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-2757-6782
Guido ReifenbergerInstitute of Neuropathology, University Hospital Düsseldorf and Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Sonika DahiyaDepartment of Pathology and Immunology, Washington University, St. Louis, Missouri, USA.ORCID 0000-0002-5585-0964
Dario CaccamoDepartment of Pathology, Sutter Medical Center, Sacramento.
Arie PerryDepartment of Pathology, San Francisco, California, USA.
University of California, San Francisco · USDüsseldorf University Hospital · DEMayo Clinic · USSutter Medical Center · USWashington University in St. Louis · US

Funding

Training Program in Translational Brain Tumor ResearchT32CA151022 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2010 to 2026
$6.6M
NCI NIH HHS T32 CA151022
6 · The paper itself

Abstract

Anaplastic meningiomas can have a sarcomatous appearance on histology but true sarcomatous (metaplastic) differentiation is rare. These tumors follow an aggressive clinical course with recurrence and poor clinical outcomes. Due to significant overlap in morphology and immunohistochemical profiles, distinguishing between sarcomatous transformation of a meningioma and a true sarcoma can be challenging. Here, we outline potential diagnostic pitfalls and the utility of ancillary molecular testing in 3 patients diagnosed with sarcomatous meningiomas. We report loss of typical meningothelial markers in sarcomatous meningiomas. Ancillary molecular testing can support the diagnosis of sarcomatous meningioma when a molecular signature consistent with meningioma is seen, such as inactivation of the NF2 gene. Recognition of this rare transformation in meningioma can prevent a misdiagnosis of a primary sarcoma, whether sporadic or radiation-induced from prior treatment of a more classic meningioma.

Indexed as

AdultAgedBiomarkers, TumorDiagnosis, DifferentialFemaleHumansMeningeal NeoplasmsMeningiomaNeurofibromin 2SarcomaBiomarkers, TumorNeurofibromin 2NF2 protein, humanAnaplasticMeningiomaMolecularNeuropathologySarcomatous

Identifiers

PMID34128073
PMCPMC9432138
OpenAlexW3170385169

What OpenQuestion holds

Textmetadata
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.