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Table of Contents - WOC 2012

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<strong>WOC</strong><strong>2012</strong> Abstract Book<br />

Neuro-ophthalmology<br />

PO-NEO-01<br />

Intracranial pathology detection by brain magnetic resonance<br />

imaging in young children with apparently isolated nystagmus<br />

Khan Arif (1) , Shammari Mansoor (1) , Elkhamary Sahar (1)<br />

1. King Khaled Eye Specialist Hospital<br />

PURPOSE: To assess incidence <strong>of</strong> intracranial pathology in young children<br />

who had brain magnetic resonance imaging (MRI) to investigate apparentlyisolated<br />

nystagmus <strong>of</strong> unclear duration.<br />

Methods: Retrospective institutional review (2003-2008).<br />

Results: Twenty-six children under 6 years old (17 boys, 9 girls) were identified.<br />

Seventeen cases (65%) were described as horizontal pendular, 5 (19%) as<br />

horizontal jerk, 2 (8%) as vertical pendular, and one each as downbeat and<br />

torsional (8%). Three <strong>of</strong> the 26 patients (12%) had significant MRI findings,<br />

all 3 <strong>of</strong> whom had temporal optic nerve head pallor noted during clinical<br />

examination. One was an otherwise normal 7-month-old girl with bilateral<br />

torsional nystagmus for whom MRI revealed a suprasellar craniopharyngioma.<br />

The second was an otherwise developmentally-normal 7-month old boy with<br />

bilateral horizontal pendular nystagmus for whom MRI revealed a retrosellar<br />

craniopharyngioma. The third was a 10-month-old boy with developmental<br />

delay and bilateral horizontal pendular nystagmus for whom MRI revealed<br />

periventricular leukomalacia and encephalomalacia.<br />

Conclusions: The optic nerve head should be carefully assessed for signs <strong>of</strong><br />

pallor in young children with nystagmus and if present brain MRI should<br />

be performed. Otherwise, isolated early childhood nystagmus without<br />

developmental delay is unlikely to be associated with intracranial pathology.<br />

PO-NEO-02<br />

Ocular Ischemic Syndrome Secondary to stenosis <strong>of</strong> intracavernous<br />

internal carotid artery.<br />

Bashir Yasfir (1) , Gul Alia (1) , Priya B V (1) , Kumar yadav Naresh (1)<br />

1. Narayana Nethralaya Eye Institute<br />

Purpose: To demonstrate the clinical presentation <strong>of</strong> Ocular Ischemic<br />

Syndrome secondary to stenosis <strong>of</strong> intracavernous internal carotid artery.<br />

Methods: A 67 year old male,diabetic and hypertensive presented with history<br />

<strong>of</strong> progressive visual loss <strong>of</strong> one month duration in the right eye.Examination<br />

revealed RAPD with rubeosis iridis and normal IOP. Gonioscopy showed<br />

open angles with new vessels .Fundus examination and angiography showed<br />

features suggestive <strong>of</strong> Ocular Ischemic Syndrome (OIS).Carotid Doppler<br />

ultrasound did not reveal any significant stenosis. He underwent panretinal<br />

laser photocoagulation and presented 3 weeks later with no perception <strong>of</strong> light<br />

and hemicranial headache and was advised neuro-imaging.<br />

Results: A CT carotid angiography showed 90% blockage <strong>of</strong> right supraclinoid<br />

internal carotid artery(intracavernous portion) which was missed on carotid<br />

Doppler USG .<br />

Conclusion: In cases with high suspicion <strong>of</strong> ocular ischemia, routine<br />

investigations like Echocardiography and carotid Doppler USG may not be<br />

sensitive enough to detect intracranial carotid artery stenosis and specialized<br />

diagnostic modalities like CT angiography or MR angiography may be needed.<br />

542<br />

PO-NEO-03<br />

Ocular Manifestations <strong>of</strong> Intracranial Space Occupying Lesions- A<br />

Retrospective Study<br />

Parija Sucheta (1) , Sharat Soumya (1)<br />

1. SCB Medical College and Hospital, Utkal University<br />

Purpose: To study the ocular manifestations <strong>of</strong> intracranial space occupying<br />

lesions (ICSOL).<br />

Methods: A retrospective study <strong>of</strong> 42 cases clinico-radiologically diagnosed as<br />

ICSOL had comprehensive ophthalmologic examination during March 2009 to<br />

July 2010 at a tertiary hospital. Informed consent was taken, and a pr<strong>of</strong>orma<br />

was filled regarding demographic data, medical and surgical history and<br />

management.<br />

Results: The significant age group affected was 20-40 years (54.8%). Most<br />

common ocular manifestation was papilledema, bilateral in 94.4% and<br />

unilateral in 5.6%. Visual acuity (OU) was 6/60 in 80.9%.<br />

Loss <strong>of</strong> corneal sensation in 11.9%, 6th nerve palsy in 14.3%, coarse horizontal<br />

nystagmus in 4.8%, bitemporal hemianopia in 4.8%, and diplopia in 7.1% were<br />

observed. Major etiological factor was frontal lobe gliomas in 47.6%, followed<br />

by meningiomas in 26.2%, pituitary tumours in 4.8%, lymphomas in 4.8% and<br />

others in 7.1%.<br />

Conclusion: Bilateral papilledema is the most common ocular manifestation <strong>of</strong><br />

ICSOL. Sudden deterioration <strong>of</strong> vision generates the need for early detection<br />

<strong>of</strong> papilledema with ICSOL and timely referral for neurosurgical intervention.<br />

PO-NEO-04<br />

Subtle ocular albinism and multifocal ERG in darkly pigmented<br />

patients with congenital nystagmus<br />

Shehri Mohamed (1) , galves alberto (1) , arishi nawal (1) , ghazi nicola (1)<br />

1. King Khalid Eye Specialist Hospital (KKESH)<br />

Purpose: to include the ocular or Oculocutaneous albinism in the differential<br />

diagnosis <strong>of</strong> darkly pigmented patients with congenital nystagmus & to show<br />

the role <strong>of</strong> multifocal ERG to diagnose foveal hypoplasia. Method: Case<br />

series <strong>of</strong> subtle ocular albinism in darkly pigmented patients presented to<br />

neurophthalmology clinic with congenital nystagmus.<br />

Results: patients with congenital nystagmus and decreased VA since early<br />

childhood; clinically they are darkly pigmented people with horizontal<br />

nystagmus, in careful slit lamp exam there is very subtle iris transillumination<br />

defects and abnormal foveal reflex. Global ERG was normal but the multifocal<br />

ERG shows a flat response documents a foveal hypoplasia.<br />

Conclusion: in neurophthalmology clinic pts with congenital nystagmus should<br />

be evaluated to roll out albinism even if darkly pigmented, by careful exam <strong>of</strong><br />

iris and fovea with possible use <strong>of</strong> multifocal ERG.<br />

PO-NEO-05<br />

Alternative method <strong>of</strong> injection <strong>of</strong> kenalog at treatment <strong>of</strong> neuritis <strong>of</strong><br />

optic nerve<br />

Dzhumagulov Olzhobai (1) , Gaidamac Victoria (1) , Eshmambetov Asizbec (1)<br />

1. Kyrgyz State Medical Academy<br />

Purpose: To desing new method <strong>of</strong> injection <strong>of</strong> corticosteroid - kenalog at<br />

neuritis <strong>of</strong> optic nerve.<br />

Methods: At the first stage <strong>of</strong> work, technique <strong>of</strong> operation and also possible<br />

morphologic consequences <strong>of</strong> ingection <strong>of</strong> prolongated corticosteroid - kenalog<br />

into back section <strong>of</strong> eyeglobe have been studied on experimental animals.<br />

Results: At microscopic investigation <strong>of</strong> obtained specimen, it wasrevealed that<br />

our intervention did not cause any morphologic disorders <strong>of</strong> optic nerve. At the<br />

second stage, we applied drug-kenalog for patients with neutitis <strong>of</strong> optic nerve<br />

in hospital.<br />

Conclusion: Method <strong>of</strong> subtenon injection <strong>of</strong> kenalog into patients with neuritis<br />

<strong>of</strong> optic nerve at start period <strong>of</strong> disease can be considered as one <strong>of</strong> the safest<br />

options <strong>of</strong> treatment <strong>of</strong> neuritis <strong>of</strong> optic nerve.

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