Non‐Arteritic Anterior Ischaemic Optic Neuropathy and Its Masquerades: A Comprehensive Diagnostic Review

Non-arteritic anterior ischaemic optic neuropathy (NAION) is the most common acute optic neuropathy in individuals over 50 years and presents with sudden, painless vision loss. However, due to the limited phenotypic repertoire of optic nerve injury, other conditions can closely mimic NAION, leading to diagnostic uncertainty. This review outlines the key clinical, imaging and systemic features that help differentiate NAION from its major masquerades, including arteritic anterior ischaemic optic neuropathy, demyelinating optic neuritis, autoimmune and granulomatous diseases, hereditary optic neuropathies, incipes and vascular abnormalities. Particular attention is given to the diagnostic pitfalls and red flags that should prompt reconsideration of the diagnosis. A hypothesis-driven approach based on history, examination and targeted investigations is essential to avoid misdiagnosis and inappropriate management. Recognising atypical features early can significantly alter prognosis and guide timely and appropriate therapy.

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Publication Details

Journal
Clinical and Experimental Ophthalmology
Published
2026-03-16
DOI
https://doi.org/10.1111/ceo.70061
Primary Topic
Intraoperative Neuromonitoring and Anesthetic Effects
Type
article
Field-Weighted Citation Impact
0.00
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article

Non‐Arteritic Anterior Ischaemic Optic Neuropathy and Its Masquerades: A Comprehensive Diagnostic Review

Alexandra Lawrence, Helen V. Danesh‐Meyer, Peter J. Savino
Clinical and Experimental Ophthalmology
Intraoperative Neuromonitoring and Anesthetic Effects
article

Non‐Arteritic Anterior Ischaemic Optic Neuropathy and Its Masquerades: A Comprehensive Diagnostic Review

Alexandra Lawrence, Helen V. Danesh‐Meyer, Peter J. Savino
article en

Abstract

Non-arteritic anterior ischaemic optic neuropathy (NAION) is the most common acute optic neuropathy in individuals over 50 years and presents with sudden, painless vision loss. However, due to the limited phenotypic repertoire of optic nerve injury, other conditions can closely mimic NAION, leading to diagnostic uncertainty. This review outlines the key clinical, imaging and systemic features that help differentiate NAION from its major masquerades, including arteritic anterior ischaemic optic neuropathy, demyelinating optic neuritis, autoimmune and granulomatous diseases, hereditary optic neuropathies, incipes and vascular abnormalities. Particular attention is given to the diagnostic pitfalls and red flags that should prompt reconsideration of the diagnosis. A hypothesis-driven approach based on history, examination and targeted investigations is essential to avoid misdiagnosis and inappropriate management. Recognising atypical features early can significantly alter prognosis and guide timely and appropriate therapy.

Clinical and Experimental Ophthalmology
University of Auckland (NZ), Northland District Health Board (NZ), Smith-Kettlewell Eye Research Institute (US), Glaucoma Research Foundation (US)
Good health and well-being
Openalex Percentile: Top 21%
Intraoperative Neuromonitoring and Anesthetic Effects
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