Evidence map›Paper›PMID 42607342›Full record

ArticleJournal of neurosurgery. Case lessons2026

Central-variant posterior reversible encephalopathy syndrome mimicking tumor progression in a glioblastoma patient on bevacizumab: illustrative case.

Yusuke Kobayashi, Yuta Kawauchi, Yosuke Sato, Tomomi Yoshiyama, Ikuya Natori, Daisuke Tanioka, Yoichi Morofuji

Abstract read
In one paragraph

Article in Journal of neurosurgery. Case lessons, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Yusuke KobayashiDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.ORCID 0009-0001-6216-7119
Yuta KawauchiDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.
Yosuke SatoDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.
Tomomi YoshiyamaDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.ORCID 0009-0006-3845-5205
Ikuya NatoriDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.
Daisuke TaniokaDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.
Yoichi MorofujiDepartment of Neurosurgery, Showa Medical University School of Medicine, Tokyo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBevacizumab (BEV) has been associated with posterior reversible encephalopathy syndrome (PRES). Central-variant PRES (cvPRES), involving the thalami and periventricular regions, can mimic glioblastoma (GBM) recurrence. Few reports have described this pattern assessed by serial quantitative apparent diffusion coefficient (ADC) measurement with BEV continuation. OBSERVATIONS: A 36-year-old woman with IDH-mutant GBM of the left frontal lobe, treated with resection, radiotherapy, temozolomide, and subsequently BEV at recurrence, presented 6 weeks after her ninth BEV cycle with impaired consciousness and gait disturbance. Family blood pressure (BP) records revealed systolic variability of 90-200 mm Hg with temporal correlation between systolic peaks and neurological worsening. MRI showed periventricular fluid-attenuated inversion recovery hyperintensity extending into the bilateral medial thalami, faint patchy enhancement, and elevated ADC. Symptoms improved within days of antihypertensive optimization; at 5 months, imaging nearly resolved and quantitative ADC measurement showed near-complete normalization (normalized ADC [nADC] 1.42 → 1.00). BEV was continued under strict BP management. LESSONS: In GBM patients on BEV, a lesion with 1) central/periventricular/thalamic distribution, 2) absent nodular/ring enhancement, 3) elevated ADC, 4) temporal correlation between BP fluctuation and symptoms, and 5) prompt reversibility with antihypertensive optimization should suggest cvPRES over recurrence. ADC normalization supports reversibility, and BEV continuation under strict BP control is reasonable in recurrent GBM. https://thejns.org/doi/10.3171/CASE26614.

Indexed as

bevacizumabcase reportcentral variantposterior reversible encephalopathy syndromerecurrent glioblastoma

Identifiers

PMID42607342
PMCPMC13479754

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.