Evidence map›Paper›PMID 42176297›Full record

ArticleThe American journal of case reports2026

Isolated Unilateral Oculomotor Neuropathy Following A Presumed Infection Treated With Corticosteroids in a Child.

Fuad Almalki

Abstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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

1 author.

Fuad AlmalkiDepartment of Pediatrics, College of Medicine, Majmaah University, Majmaah, Saudi Arabia.ORCID 0000-0003-3856-7697

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Oculomotor neuropathy represents a very small proportion of cranial nerve palsies in children. It may result from both congenital and acquired causes. Acquired causes include vasculopathies, inflammation, infections, and neoplasms. However, only a limited number of studies in adults and children have identified post-infectious isolated oculomotor neuropathy, and even fewer have investigated the therapeutic role of corticosteroids in its treatment. CASE REPORT A previously healthy 4-year-old Saudi boy presented to the emergency department with acute onset of substantial drooping of the left upper eyelid, diplopia, and subjective low-grade fever. There were no symptoms of increased intracranial pressure and no history of head trauma. Physical examination revealed complete left-sided oculomotor neuropathy and anisocoria, without involvement of other cranial nerves or additional focal findings. Neuroimaging (computed tomography, contrast-enhanced magnetic resonance imaging, magnetic resonance angiography, and magnetic resonance venography), cerebrospinal fluid analysis, and opening pressure assessment showed normal results. Other serological findings were unremarkable. No underlying etiology was identified, and a post-infectious immune-mediated process was suspected. Oral prednisolone was initiated at a dose of 2 mg/kg/day for 5 days, followed by a 5-day taper. Follow-up at 3 months demonstrated complete resolution. CONCLUSIONS This case of isolated unilateral oculomotor neuropathy after presumed infection demonstrated complete clinical recovery after a short course of oral corticosteroids. Although a causal relationship cannot be established, such treatment may be cautiously considered in children who present with acute oculomotor neuropathy and a possible post-infectious process after an extensive, inconclusive workup. Further studies are needed to confirm this observation.

Indexed as

GlucocorticoidsOculomotor Nerve DiseasesPrednisoloneChild, PreschoolHumansMaleGlucocorticoidsPrednisolone

Identifiers

PMID42176297
PMCPMC13214597

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