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ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Fulminant idiopathic intracranial hypertension mimicking Chiari I malformation in a pediatric patient: diagnostic value of MRI and promising outcomes with venous sinus stenting.

Manel Krouma, Basile Kerleroux, Beatrice Desnous, Jean François Hak, Mathieu Milh, Didier Scavarda

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Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

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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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

6 authors.

Manel KroumaDepartment of Pediatric Neurosurgery, La Timone Hospital, Aix-Marseille University, Marseille, France.
Basile KerlerouxDepartment of Neuroradiology, La Timone Hospital, Aix-Marseille University, Marseille, France.
Beatrice DesnousDepartment of Pediatric Neurology, La Timone Hospital, Aix-Marseille University, Marseille, France.
Jean François HakDepartment of Neuroradiology, La Timone Hospital, Aix-Marseille University, Marseille, France.
Mathieu MilhDepartment of Pediatric Neurology, La Timone Hospital, Aix-Marseille University, Marseille, France.
Didier ScavardaDepartment of Pediatric Neurosurgery, La Timone Hospital, Aix-Marseille University, Marseille, France. Didier.scavarda@ap-hm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic intracranial hypertension (IIH) is a rare but potentially serious condition in children, with the risk of permanent vision loss in rapidly progressing or treatment-resistant cases. One diagnostic challenge is that cerebellar tonsillar descent-a feature sometimes seen in IIH-can mimic Chiari I malformation, potentially leading to misdiagnosis and unnecessary, risky surgery. We report the case of a 13-year-old boy with fulminant idiopathic intracranial hypertension (IIH), who presented with rapidly worsening visual symptoms and severe papilledema over the course of a few days. Initial brain MRI excluded other causes of increased intracranial pressure, raising suspicion for IIH. The imaging also revealed cerebellar tonsillar descent, initially suggesting a possible Chiari I malformation. However, additional MRI findings were more consistent with IIH than Chiari I, including an arachnoidocele of the sella, flattening of the posterior sclera, and bilateral transverse sinus stenosis. A cerebral venography confirmed significant venous outflow obstruction, with a high-pressure gradient across the stenotic transverse sinuses. Based on these findings, venous sinus stenting was performed as a first-line treatment. This resulted in rapid symptom improvement, with complete resolution of headache and papilledema on follow-up. MRI plays a critical role in diagnosis-not only in excluding other conditions but also in positively identifying IIH, especially in atypical and fulminant presentations. When medical treatment fails, surgical options include CSF shunting or increasingly, venous sinus stenting, particularly when venous sinus stenosis is present. Though commonly used in adults, this approach is showing promise in pediatric patients as well, despite some specific challenges. Early diagnosis, appropriate imaging, and a multidisciplinary approach are essential to prevent vision loss and ensure the best possible outcomes in these complex pediatric cases.

Indexed as

Arnold-Chiari MalformationCranial SinusesMagnetic Resonance ImagingPseudotumor CerebriStentsAdolescentDiagnosis, DifferentialHumansMaleChiari I malformationMRIPseudotumor cerebriVenous sinus stenting

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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.