Evidence map›Paper›PMID 40821180›Full record

ArticleCureus2025

Idiopathic Intracranial Hypertension With Sustained Normal Opening Pressure: A Case Report.

Stanley Pierre, Shantell Steele, Melissa Candela, Allison Rojas, Nayle Araguez-Ancares

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

5 authors.

Stanley PierreSurgery, Ross University School of Medicine, St. Michael, BRB.
Shantell SteeleSurgery, Ross University School of Medicine, Miramar, USA.
Melissa CandelaSurgery, American University of the Caribbean School of Medicine, Cupecoy, SXM.
Allison RojasSurgery, American University of the Caribbean School of Medicine, Cupecoy, SXM.
Nayle Araguez-AncaresInternal Medicine, Jackson Memorial Hospital, Miami, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic intracranial hypertension (IIH) is a clinical diagnosis made from the exclusion of other possible causes of increased intracranial pressure (ICP): cerebrospinal fluid (CSF) overflow obstruction, mass lesion, infection, or malignancies. IIH is a phenomenon with a rapid onset that most notably presents in obese women of childbearing age. We present the case of a 30-year-old African American woman with a past medical history of bipolar disorder who arrived at the emergency department (ED) with acute bilateral vision loss, two weeks of bilateral retro-orbital headache, painful eye movements, and progressive vision loss with a decrease in appetite. Management involved plasma exchange, high-dose steroids, consistent neurological and ophthalmic tests, and close observation and follow-up. One week after the most recent ED visit, the patient confirmed a significant improvement in vision. When diagnosing our patient with IIH, it was imperative to rule out myelinating oligodendrocyte glycoprotein antibody-associated disease (MOGAD), multiple sclerosis (MS), and other demyelinating diseases such as optic neuritis. Initial brain imaging using computed tomography (CT) without contrast showed no evidence of intracranial hemorrhage but demonstrated the presence of prominent sheath complexes, suggestive of optic neuritis, and a slightly small pituitary gland height for a patient who is 30 years of age. Further testing with a CT venogram (CTV) and a magnetic resonance imaging (MRI) of the head and neck confirmed demyelination. The patient's lumbar puncture continuously revealed a normal opening pressure during her hospital stay. This case presentation will highlight and compare the current literature regarding the clinical presentation and management of idiopathic intracranial hypertension.

Indexed as

bilateral optic neuritisintracranial idiopathic hypertensionmyelinating oligodendrocyte glycoprotein antibody-associated diseasemyelin-oligodendrocyte glycoprotein (mog)myelin sheath

Identifiers

PMID40821180
PMCPMC12350088

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