Combined subtemporal and pterional approach for clipping of multiple aneurysms

Background: Despite ongoing improvements in endovascular techniques, open surgical management of basilar apex aneurysms is occasionally necessary.[2] Critical dissection of perforating vessels from the aneurysm is facilitated by the lateral trajectory of the subtemporal approach.[1] Incorporation of additional trajectories can facilitate treatment of multiple aneurysms within the same procedure. Case Description: A 48-year-old woman presented with a Hunt and Hess 1 and Fisher Grade 3 subarachnoid hemorrhage from a small and broad-necked basilar apex aneurysm that was not amenable to endovascular management. An unruptured left A1-A2 anterior cerebral artery aneurysm was also noted on vascular imaging. The patient underwent a combined right subtemporal and pterional approach for sequential clipping of the basilar and anterior communicating artery aneurysms. The third nerve, running between the posterior cerebral artery and the superior cerebellar artery, guided dissection to the basilar artery in the subtemporal approach. A temporary clip was placed on a vessel-free zone of the basilar trunk during dissection of perforators off the posterior aspect of the aneurysm dome. A fenestrated clip around the right P1 segment was used to ensure complete occlusion of the aneurysm. Indocyanine green angiography was used to confirm successful clipping and patency of parent and perforating vessels. The unruptured A1-A2 aneurysm was clipped without difficulty from the pterional trajectory. The patient had an uneventful postoperative recovery with the exception of transient right third nerve palsy. Conclusion: As highlighted by this case, maintenance of open surgical skills for the treatment of complex aneurysms unamenable to endovascular therapies is critical.

Recurrent painful ophthalmoplegic neuropathy: a cause for recurrent third nerve palsy in a child

Recurrent painful ophthalmoplegic neuropathy (RPON), previously called ophthalmoplegic migraine, is a rare condition characterised by recurrent episodes of headache and ophthalmoplegia. We report a case of 11-year-old girl with recurrent painful ophthalmoplegia due to isolated right oculomotor nerve involvement. MR brain imaging showed enhancing lesion of cisternal segment of right oculomotor nerve. A possibility of Tolosa Hunt syndrome was considered and she was treated with glucocorticoids, followed by azathioprine due to recurrence. In the fourth episode, she developed migraine headache followed by right third nerve palsy, after which the diagnosis was revised to RPON. She was started on flunarizine along with short-term glucocorticoids. At 1-year follow-up, she remained asymptomatic. RPON should be considered in patients with recurrent third nerve palsy to avoid inadvertent long-term exposure to immunosuppressive agents.

Rare presentation of sarcoidosis with optic neuropathy and third nerve palsy

Sarcoidosis is a systemic, idiopathic and granulomatous disease, which most commonly affects the skin, lungs and lymph nodes but can affect virtually any organ. Neurosarcoidosis can be the presenting or the only clinical manifestation accounting for 5%–15% of sarcoid diagnoses. In contrast to uveitis which is the most common ophthalmic manifestation, neuro-ophthalmic signs are uncommon in sarcoidosis. Optic neuropathy is the most common neuro-ophthalmic sign (70% in one series). Sarcoid-related optic neuropathy commonly presents with a picture similar to optic neuritis. Less commonly, optic nerve involvement occurs secondary to compressive lesions, or from direct granulomatous infiltration. Neuroimaging is crucial to identify the location of the lesion. We describe a case of sarcoid-related compressive optic neuropathy and third nerve palsy and highlight the challenging nature of neurosarcoidosis in a patient without a prior diagnosis of the disease.

A Hospital-Based Study on Aetiology of Third, Fourth and Sixth Cranial Nerve Palsies

BACKGROUND Neuro-ophthalmology deals with complex systemic diseases that affect the visual system and pose a challenge for ophthalmologists. Here the focus is on the diseases of the nervous system that affect vision, ocular motility, or pupillary reflexes. Diplopia, a common symptom of cranial nerve palsy, may result from ophthalmic, orbital, or neurologic disorders. Our study intended to determine the aetiology of ocular motor nerve palsies. METHODS A cross-sectional study was conducted for two years at a tertiary care centre in South India. We evaluated 30 patients who came to the Ophthalmology OPD or were admitted, after obtaining the approval of the Ethics committee. RESULTS A total number of 30 patients who fulfilled the inclusion criteria were studied. There were 14 male and 16 female patients. The age range was 12 - 87 years with a mean age of 45 years. The highest incidence noticed was isolated sixth nerve palsy in 13 (43.3 %) patients. 11 patients had isolated third nerve palsy (36.7 %), while mixed ocular motor nerve palsies (third, fourth and sixth) were seen in 6 patients (20 %). None of them had isolated fourth nerve palsy. CONCLUSIONS  The sixth nerve continued to be the most common among the ocular motor nerve palsies. Meningitis was the major cause.  Diabetes and trauma, infections with CNS inflammation accounted for a majority of third nerve palsies.  Multiple cranial nerve palsies had varied aetiology like HIV Infection, Tolosa Hunt Syndrome, aneurysm of intracavernous part of ICA, cavernous sinus thrombosis and trauma.  The patient’s age, associated symptoms, clinical features and types of palsy are of great importance to choose appropriate radiological methods to study and treat these isolated cranial nerve palsies. KEY WORDS Diabetes, Meningitis, Oculomotor Nerve, Trochlear Nerve, Abducent Nerve, Trauma