Evidence map›Paper›PMID 39838550›Full record

ArticleBrain pathology (Zurich, Switzerland)2025

Brain-derived textiloma post glioblastoma resection and application of oxidized regenerated cellulose: A pilot, bedside-to-bench, translational study.

Joshua A Kra, Christopher Markosian, Fenny H F Tang, Ada Baisre de León, Anupama Chundury, Pankaj K Agarwalla, Daniela I Staquicini, Renata Pasqualini, Wadih Arap

Abstract readCase Reports
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors.

Joshua A KraRutgers Cancer Institute, Newark, New Jersey, USA.
Christopher MarkosianRutgers Cancer Institute, Newark, New Jersey, USA.
Fenny H F TangRutgers Cancer Institute, Newark, New Jersey, USA.
Ada Baisre de LeónDepartment of Pathology, Immunology, and Laboratory Medicine, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
Anupama ChunduryRutgers Cancer Institute, New Brunswick, New Jersey, USA.
Pankaj K AgarwallaRutgers Cancer Institute, Newark, New Jersey, USA.
Daniela I StaquiciniRutgers Cancer Institute, Newark, New Jersey, USA.
Renata PasqualiniRutgers Cancer Institute, Newark, New Jersey, USA.
Wadih ArapRutgers Cancer Institute, Newark, New Jersey, USA.ORCID 0000-0002-8686-4584

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Levy-Longenbaugh Donor-Advised FundNCI NIH HHS P30 CA072720NCI NIH HHS P30CA072720
6 · The paper itself

Abstract

Oxidized regenerated cellulose (ORC; marketed as Surgicel® and Tabotamp®) is routinely used as an intraoperative hemostatic agent. Rarely, residual ORC has been associated with a foreign body reaction generating cystic or granulomatous lesions (i.e., textilomas) at the surgical site. Here, we report a bedside-to-bench, translational report of an intracranial mass after neurosurgical resection of glioblastoma with ORC application. As part of patient care, we performed magnetic resonance imaging and histopathological analysis of the mass. We then performed in vitro studies to evaluate the effect of ORC on cytokine production and viability of BV-2 murine microglial cells by using quantitative PCR along with live cell microscopy and crystal violet staining, respectively. Magnetic resonance imaging demonstrated a recurrent mass pressing on the adjacent right ventricle, which was removed in a second surgery for diagnostic and therapeutic purposes. Unexpectedly, histopathological examination of the resected mass revealed abundant ORC arising from the site with inflammation, microglial activation, and collagenization. Mechanistically, we show an ORC-induced modest increase in inflammatory cytokines with a subsequent decrease in microglial cell viability. These findings suggest that ORC may mediate microglial immune response and viability, and serve to raise awareness and guide interpretation of post-treatment surveillance imaging findings in the instance of foreign body reaction.

Indexed as

Brain NeoplasmsCellulose, OxidizedForeign-Body ReactionGlioblastomaAnimalsBrainFemaleHumansMagnetic Resonance ImagingMaleMiceMicrogliaNeurosurgical ProceduresPilot ProjectsCellulose, OxidizedSurgicelcystic massgranulomaneurosurgerySurgicel®Tabotamp®

Identifiers

PMID39838550
PMCPMC12145898

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.