ophthalmoplegic migraine
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Author(s):  
Andrew M. Sorsby-Vargas ◽  
Alejandra Martínez-Maldonado ◽  
Claudia L. Arellano-Martínez

2021 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
MinalV Kekatpure ◽  
Pratibha Panmand ◽  
Sivakanth Nalubolu

2021 ◽  
Vol 69 (6) ◽  
pp. 1805
Author(s):  
Anwar Alam ◽  
MdShahid Iqubal ◽  
Baidyanath Kumar ◽  
ZeyaurR Azad

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 1219 ◽  
Author(s):  
Robin M. van Dongen ◽  
Joost Haan

Migraine is a common headache disorder characterized by often-severe headaches that may be preceded or accompanied by a variety of visual symptoms. Although a typical migraine aura is not difficult to diagnose, patients with migraine may report several other visual symptoms, such as prolonged or otherwise atypical auras, “visual blurring”, “retinal migraine”, “ophthalmoplegic migraine”, photophobia, palinopsia, and “visual snow”. Here, we provide a short overview of these symptoms and what is known about the relationship with migraine pathophysiology. For some symptoms, the association with migraine is still debated; for other symptoms, recent studies indicate that migraine mechanisms play a role.


2019 ◽  
Vol 9 (3) ◽  
pp. 256-262 ◽  
Author(s):  
Vivek Lal ◽  
Louis Caplan

The 3rd edition of the International Classification of Headache Disorders replaced the term ophthalmoplegic migraine (OM) with Recurrent Painful Ophthalmoplegic Neuropathy (RPON) based on the presence of contrast enhancement of the involved cranial nerves on Gadolinium-enhanced magnetic resonance imaging. We review our experience and publications concerning ophthalmoplegia, migraine, and RPON. Majority of cases of acute ophthalmoplegia are associated with severe migrainous headaches. A positive history of migraine, increased severity of migraine headaches before the onset of ophthalmoplegia, and the close temporal association between migraine attacks and ophthalmoplegia all suggest an important role played by migraine in the causation of ophthalmoplegia. Enhancement of the involved cranial nerves may be due to the neuro-inflammatory cascade associated with migraine. OM should be considered along with RPON in differential diagnoses of painful ophthalmoplegic syndromes.


2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Laura N. Zamproni ◽  
Reinaldo T. Ribeiro ◽  
Marina Cardeal

Recurrent painful ophthalmoplegic neuropathy, previously known as ophthalmoplegic migraine, is a rare condition that affects children and young adults. Its cause and classification are still controversial and, consequently, there are no published treatment guidelines or consensus. Glucocorticoids seem to be beneficial for some patients, but there is no established treatment when failure of this therapy occurs. The aim of this study was to report a case where pregabalin was successfully used after failure of glucocorticoid therapy in a patient with recurrent painful ophthalmoplegic neuropathy.


2018 ◽  
Vol 6 (3) ◽  
pp. 114-117
Author(s):  
Sharmila Segar ◽  
Chandni Duphare ◽  
Osemelu Aburime

Background: Recurrent painful ophthalmoplegic neuropathy (RPON), formerly known as ophthalmoplegic migraine (OM), is a poorly understood condition that presents with recurrent unilateral headaches and at least one ocular cranial nerve (CN) palsy, generally in childhood. There has been ongoing debate about whether the etiology of this disorder is neuropathic or related to migraines. The Case: We present a case about a 10-year-old male with his third presentation of RPON, repeatedly affecting his right oculomotor nerve. His treatment choices are discussed, along with associated outcomes. The patient was treated with topiramate with resolution of his symptoms occurred within one month. Conclusion: As the annual incidence of RPON is rare at fewer than 1 case per million people, clear documentation of observed cases with treatment failures and successes is key to building evidence for future management.


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