Evidence map›Paper›PMID 42698425›Full record

ArticleFrontiers in neurology2026

Orbital apex syndrome from middle meningeal artery embolization.

Andrew Trippiedi, Andrew F Fischer, Michael Dattilo

Abstract readCase Reports
In one paragraph

Article in Frontiers in neurology, 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
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1 · What the graph read from it

What it found

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2 · The registry

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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

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5 · Who and what money

Authors and funding

3 authors.

Andrew TrippiediDepartment of Ophthalmology, Emory University School of Medicine, Atlanta, GA, United States.
Andrew F FischerDepartment of Ophthalmology, Emory University School of Medicine, Atlanta, GA, United States.
Michael DattiloDepartment of Ophthalmology, Emory University School of Medicine, Atlanta, GA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To present two cases of orbital apex syndrome, a previously unreported complication of middle meningeal artery (MMA) embolization. Background: MMA embolization is increasingly used to treat chronic subdural hematomas and is generally considered safe. However, anastomotic connections to the ophthalmic circulation may permit complications from embolic migration. Methods: Retrospective case series of two patients who developed neuro-ophthalmic complications following MMA embolization for subdural hematoma. Results: A 75-year-old male developed acute diplopia, a relative afferent pupillary defect (RAPD), and ophthalmoplegia shortly after MMA embolization. Magnetic resonance imaging demonstrated embolic material in the posterior orbit. He was diagnosed with an orbital apex syndrome and treated with intravenous steroids with improvement in ocular motility and alignment and resolution of his RAPD. A 44-year-old male presented 1 year after MMA embolization with progressive diplopia, ptosis, and visual loss. Examination revealed an optic neuropathy, and multiple cranial neuropathies consistent with an orbital apex syndrome. He was treated with oral steroids and had improvement in his vision and oculomotor examination. Conclusions: Case reports of ophthalmic complications from MMA embolization have reported transient cranial neuropathies or isolated ischemic events, presumably through unintended migration of embolic material through under-recognized meningo-ophthalmic anastomoses. These cases are the first report of orbital apex syndrome as a potential complication of MMA embolization.

Indexed as

Embolization, TherapeuticMeningeal ArteriesOphthalmoplegiaAdultAgedDiplopiaHumansMaleRetrospective StudiesSyndromecase reportdiplopiaMiddle meningeal artery embolization (MMAE)middle meningeal artery (MMA)orbital apex syndrome

Identifiers

PMID42698425
PMCPMC13541464

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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.