Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review

Background. Recurrent painful ophthalmoplegic neuropathy (RPON), previously known as ophthalmoplegic migraine (OM), is an uncommon disorder with repeated episodes of ocular cranial nerve neuropathy associated with ipsilateral headache. The age of presentation is most often during childhood or adoles...

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Main Authors: Maria Giuseppina Petruzzelli, Mariella Margari, Flora Furente, Maria Carmela Costanza, Anna Rosi Legrottaglie, Franca Dicuonzo, Lucia Margari
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Pain Research and Management
Online Access:http://dx.doi.org/10.1155/2019/5392945
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author Maria Giuseppina Petruzzelli
Mariella Margari
Flora Furente
Maria Carmela Costanza
Anna Rosi Legrottaglie
Franca Dicuonzo
Lucia Margari
author_facet Maria Giuseppina Petruzzelli
Mariella Margari
Flora Furente
Maria Carmela Costanza
Anna Rosi Legrottaglie
Franca Dicuonzo
Lucia Margari
author_sort Maria Giuseppina Petruzzelli
collection DOAJ
description Background. Recurrent painful ophthalmoplegic neuropathy (RPON), previously known as ophthalmoplegic migraine (OM), is an uncommon disorder with repeated episodes of ocular cranial nerve neuropathy associated with ipsilateral headache. The age of presentation is most often during childhood or adolescence. MRI has a central role in the assessment of the RPON, especially to distinguish orbital, parasellar, or posterior fossa lesions that mimic symptoms of RPON. Actually, oculomotor nerve tumors may be masquerade as RPON so that MRI follow-ups are required to detect the possibility of tumor etiology. Case presentation. We report a 16-year-old boy with a 7-year follow-up and multiple brain MRI data, previously diagnosed as OM. The last brain MRI, performed during an acute phase of oculomotor paresis with ipsilateral headache, showed a nodular lesion described as schwannoma of III cranial nerve. Then, we reviewed the literature on OM and RPON in pediatric age with a focus on brain MRI findings. Conclusions. This review highlights the important role of serial brain MRIs in the long-term follow-up of RPON, especially in the cases with childhood onset, in order to not delay the diagnosis of a possible oculomotor nerve schwannoma.
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spelling doaj-art-53cae715b33f49c6b0f2131c43625ed92025-02-03T07:24:38ZengWileyPain Research and Management1203-67651918-15232019-01-01201910.1155/2019/53929455392945Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature ReviewMaria Giuseppina Petruzzelli0Mariella Margari1Flora Furente2Maria Carmela Costanza3Anna Rosi Legrottaglie4Franca Dicuonzo5Lucia Margari6Department of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari “Aldo Moro”, Bari, ItalyBackground. Recurrent painful ophthalmoplegic neuropathy (RPON), previously known as ophthalmoplegic migraine (OM), is an uncommon disorder with repeated episodes of ocular cranial nerve neuropathy associated with ipsilateral headache. The age of presentation is most often during childhood or adolescence. MRI has a central role in the assessment of the RPON, especially to distinguish orbital, parasellar, or posterior fossa lesions that mimic symptoms of RPON. Actually, oculomotor nerve tumors may be masquerade as RPON so that MRI follow-ups are required to detect the possibility of tumor etiology. Case presentation. We report a 16-year-old boy with a 7-year follow-up and multiple brain MRI data, previously diagnosed as OM. The last brain MRI, performed during an acute phase of oculomotor paresis with ipsilateral headache, showed a nodular lesion described as schwannoma of III cranial nerve. Then, we reviewed the literature on OM and RPON in pediatric age with a focus on brain MRI findings. Conclusions. This review highlights the important role of serial brain MRIs in the long-term follow-up of RPON, especially in the cases with childhood onset, in order to not delay the diagnosis of a possible oculomotor nerve schwannoma.http://dx.doi.org/10.1155/2019/5392945
spellingShingle Maria Giuseppina Petruzzelli
Mariella Margari
Flora Furente
Maria Carmela Costanza
Anna Rosi Legrottaglie
Franca Dicuonzo
Lucia Margari
Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
Pain Research and Management
title Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
title_full Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
title_fullStr Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
title_full_unstemmed Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
title_short Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review
title_sort recurrent painful ophthalmoplegic neuropathy and oculomotor nerve schwannoma a pediatric case report with long term mri follow up and literature review
url http://dx.doi.org/10.1155/2019/5392945
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