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Journal of Pediatric Neurology 2024; 22(01): 064-067
DOI: 10.1055/s-0042-1760197
Case Report

Recurrent Painful Ophthalmoplegic Neuropathy Mistaken for Oculomotor Schwannoma: A Case Report

Darija Mahović 
1   Department of Neurology, University Hospital Center Zagreb, School of Medicine, University of Zagreb, Zagreb, Croatia
,
Matea Bračić 
2   Department of School and Adolescent Medicine, Andrija Štampar Teaching Institute of Public Health, Zagreb, Croatia
,
Ivan Jovanović
3   Department of Neuroradiology, University Hospital Center Zagreb, Zagreb, Croatia
,
Ivo Darko Gabrić 
4   Department of Cardiology, University Hospital Center “Sestre Milosrdnice,” School of Medicine, Croatian Catholic University, Zagreb, Croatia
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Abstract

Recurrent painful ophthalmoplegic neuropathy (RPON) is a headache disorder classified as a cranial neuropathy. It is characterized by episodes of unilateral headache followed by ipsilateral ophthalmoplegia due to ocular cranial nerve palsy. Symptoms usually subside spontaneously within weeks to months. RPON commonly occurs in childhood, though it is overlooked at times as a possible differential diagnosis. The pathophysiology of RPON is not entirely clear. Typical magnetic resonance imaging (MRI) findings in children include nerve thickening and gadolinium enhancement. However, these findings are not specific to this condition. Nerve thickening in RPON can resemble schwannomas, thereby causing a diagnostic dilemma. Here, we present a 13-year-old boy with a history of unilateral headaches associated with ipsilateral ptosis and diplopia. The first MRI indicated thickening and gadolinium enhancement of the right oculomotor nerve, which was interpreted as a schwannoma. However, his symptoms resolved after a few weeks and the follow-up MRI showed resolution of nerve changes. This clinical presentation was consistent with RPON. This case demonstrates the need for a careful follow-up of RPON patients.

Keywords

recurrent painful ophthalmoplegic neuropathy - headache - schwannoma - case report

Consent

Written informed consent for publication was obtained from the patient's parents.




Publication History

Received: 26 July 2022

Accepted: 20 November 2022

Article published online:
30 December 2022

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