Aberrant regeneration of the oculomotor nerve: implications for neurosurgeons

2007 ◽  
Vol 23 (5) ◽  
pp. E14 ◽  
Author(s):  
Eric D. Weber ◽  
Steven A. Newman

✓Aberrant regeneration of cranial nerve III, otherwise known as oculomotor synkinesis, is an uncommon but well-described phenomenon most frequently resulting from trauma, tumors, and aneurysms. Its appearance usually follows an oculomotor palsy, but it can also occur primarily without any preceding nerve dysfunction. It is vital that neurosurgeons recognize this disorder because it may be the only sign of an underlying cavernous tumor or PCoA aneurysm. The tumor most often implicated is a cavernous or parasellar meningioma, but any tumor that causes compression or disruption along the course of the oculomotor nerve may cause primary or secondary misdirection. The most common clinical signs of oculomotor synkinesis consist of elevation of the upper eyelid on attempted downward gaze or adduction, adduction of the eye on attempted upward or downward gaze, and constriction of the pupil on attempted adduction. The authors present the largest series of patients with oculomotor synkinesis, including those in whom it developed after neurosurgical intervention, to illustrate various presentations. In addition, the various mechanisms that contribute to synkinesis are reviewed. Last, the treatment strategies for both oculomotor palsies and synkinesis are discussed.

Neurosurgery ◽  
1982 ◽  
Vol 10 (4) ◽  
pp. 490-491 ◽  
Author(s):  
Takashi Iwabuchi ◽  
Mikio Suzuki ◽  
Tsutomu Nakaoka ◽  
Shigeharu Suzuki

Abstract We report a patient who underwent anastomosis of the left oculomotor nerve, which had been inadvertently and bluntly severed during the resection of a left parasellar chromophobe pituitary adenoma. Neural regeneration was confirmed by the reappearance of voluntary adduction of the eyeball, clinical signs of aberrant regeneration, and the appearance of an action potential on electromyography of the levator palpebrae superioris muscle 1 year after end-to-end anastomosis of the nerve.


Author(s):  
Shirley H. Wray

is the longest chapter in the book and perhaps the most important. Syndromes of the oculomotor nuclear complex, the fasciculus and the nerve[BluM2] include disorders such as acute dilation of the pupil due to uncal herniation, aneurysmal compression of the nerve with pupil involvement or with pupil sparing, and microinfarction of the nerve with pupil sparing due to ischemia associated diabetes mellitus. Important syndromes of the sphenocavernous sinus characterized by painful ophthalmoplegia are generally associated with multiple unilateral cranial nerve palsies. Common lesions include aneurysms, meningiomas, pituitary tumors, lymphoma, and infectious and idiopathic granulomatous infiltration (the Tolosa-Hunt syndrome). A patient with primary aberrant regeneration of the oculomotor nerve due to prolonged compression by a meningioma in the cavernous sinus is illustrated by video display.


1975 ◽  
Vol 43 (1) ◽  
pp. 95-97 ◽  
Author(s):  
James R. Keane

✓ This 6-year-old boy, after recovery from prolonged coma following head trauma, exhibited the rare phenomenon of bilateral oculomotor nerve misdirection manifested by ipsilateral eyelid elevation on adduction of either eye.


2012 ◽  
Vol 48 (5) ◽  
pp. 359-365 ◽  
Author(s):  
Brandon L. Plattner ◽  
Marc Kent ◽  
Brian Summers ◽  
Simon R. Platt ◽  
A. Courtenay Freeman ◽  
...  

A 3.5 yr old Saint Bernard was evaluated for nonambulatory tetraparesis and cranial nerve dysfunction, and a 7 yr old rottweiler was evaluated for progressive paraparesis. Clinical signs of left-sided vestibular and general proprioceptive ataxia and cranial nerve VII dysfunction in the Saint Bernard suggested a lesion affecting the brain stem. Signs in the rottweiler consisted of general proprioceptive/upper motor neuron paraparesis, suggesting a lesion involving the third thoracic (T3) to third lumbar (L3) spinal cord segments. MRI was normal in the Saint Bernard, but an intra-axial lesion involving the T13–L2 spinal cord segments was observed in the rottweiler. In both dogs, the central nervous system (CNS) contained neoplastic cells with features consistent with gliomatosis cerebri (GC). In the Saint Bernard, neoplastic cells were present in the medulla oblongata and cranial cervical spinal cord. In the rottweiler, neoplastic cells were only present in the spinal cord. Immunohistochemistry disclosed two distinct patterns of CD18, nestin, and vimentin staining. GC is a rarely reported tumor of the CNS. Although GC typically involves the cerebrum, clinical signs in these two dogs reflected caudal brainstem and spinal cord involvement.


2021 ◽  
Vol 8 (4) ◽  
Author(s):  
Marco LA GRUA ◽  
Irene GRAZZINI ◽  
Gian L. CUNEO ◽  
Gianfranco SINDACO ◽  
Matteo ZANELLA ◽  
...  

2020 ◽  
Vol 8 (3) ◽  
pp. 1092-1094
Author(s):  
V Rajesh Prabu ◽  
◽  
Rajlaxmi B Wasnik ◽  
Parul Priyambada ◽  
Ranjini H ◽  
...  

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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