51 research outputs found

    Nodular posterior scleritis mimicking choroidal metastasis: a report of two cases

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    Posterior scleritis is a rare underdiagnosed condition that can potentially cause blindness. Its varied presentations lead to delayed or incorrect treatment. We present here the cases of two patients with nodular posterior scleritis mimicking a choroidal metastasis. Two female patients presented with a sudden unilateral visual loss associated with ocular pain. Fundus examination revealed temporomacular choroidal masses with exudative detachments that, due to angiographic presentation, were suggestive of choroidal metastasis. Systemic examinations were unremarkable. In the two cases, a local or general anti-inflammatory treatment led to the complete recovery of the lesions, which were, thus, considered nodular posterior scleritis. The diagnosis of nodular posterior scleritis has to be evoked in all patients presenting with a choroidal mass in fundus examination. It represents the principal curable differential diagnosis of malignant choroidal tumor

    Diffuse laser illumination for Maxwellian view Doppler holography of the retina

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    We describe the advantages of diffuse illumination in laser holography for ophthalmology. The presence of a diffusing element introduces an angular diversity of the optical radiation and reduces its spatial coherence, which spreads out the energy distribution of the illumination beam in the focal plane of the eyepiece. The field of view of digitally computed retinal images can easily be increased as the eyepiece can be moved closer to the cornea to obtain a Maxwellian view of the retina without compromising ocular safety. Compliance with American and European safety standards for ophthalmic devices is more easily obtained by preventing the presence of a laser hot spot observed in front of the cornea in the absence of a scattering element. Diffuse laser illumination does not introduce any adverse effects on digitally computed laser Doppler images.Comment: 9 page

    Extracorporeal Membrane Oxygenation for Severe Acute Respiratory Distress Syndrome associated with COVID-19: An Emulated Target Trial Analysis.

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    RATIONALE: Whether COVID patients may benefit from extracorporeal membrane oxygenation (ECMO) compared with conventional invasive mechanical ventilation (IMV) remains unknown. OBJECTIVES: To estimate the effect of ECMO on 90-Day mortality vs IMV only Methods: Among 4,244 critically ill adult patients with COVID-19 included in a multicenter cohort study, we emulated a target trial comparing the treatment strategies of initiating ECMO vs. no ECMO within 7 days of IMV in patients with severe acute respiratory distress syndrome (PaO2/FiO2 <80 or PaCO2 ≥60 mmHg). We controlled for confounding using a multivariable Cox model based on predefined variables. MAIN RESULTS: 1,235 patients met the full eligibility criteria for the emulated trial, among whom 164 patients initiated ECMO. The ECMO strategy had a higher survival probability at Day-7 from the onset of eligibility criteria (87% vs 83%, risk difference: 4%, 95% CI 0;9%) which decreased during follow-up (survival at Day-90: 63% vs 65%, risk difference: -2%, 95% CI -10;5%). However, ECMO was associated with higher survival when performed in high-volume ECMO centers or in regions where a specific ECMO network organization was set up to handle high demand, and when initiated within the first 4 days of MV and in profoundly hypoxemic patients. CONCLUSIONS: In an emulated trial based on a nationwide COVID-19 cohort, we found differential survival over time of an ECMO compared with a no-ECMO strategy. However, ECMO was consistently associated with better outcomes when performed in high-volume centers and in regions with ECMO capacities specifically organized to handle high demand. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/)

    Visual function and retinal nerve fiber layer thickness in Neuromyelitis optica: a longitudinal and comparative study

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    Longitudinal studies in multiple sclerosis (MS) show that visual function decreases as a function of time and is correlated with a thickening of the retinal nerve fiber layer (RNFL) measured by optical coherence tomography (OCT). We determined the outcome of visual acuity and RNFL thickness in Neuromyelitis optica (NMO) in the lack of clinical relapse

    Ocular Oscillations in the Neuromyelitis Optica Spectrum

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    Four French West Indian women complained of oscillopsia and were found to have an acquired eye movement disorder. In 3 of them, different types of nystagmus were found, including upbeat, downbeat, and central form of vestibular nystagmus. One developed opsoclonus-myoclonus syndrome. Three patients had neuromyelitis optica antibodies, and 3 had brainstem abnormalities detected on MRI. Two patients had definite NMO, while the other 2 were considered to be at high risk for developing NMO. Treatment with high-dose systemic corticosteroids, with plasma exchanges, or in combination led to resolution of oscillopsia. We propose that eye movement disorders be added to the neurological manifestations of NMO

    Ocular Motor Cranial Nerve Palsies In Pituitary Apoplexy

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    Vertical Diplopia secondary to Skew Deviation with Ocular Tilt Reaction with Multiple Posterior Fossa Metastases

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    This is a case of multiple brain metastases in the posterior fossa resulting in a skew deviation. Figure 1 : Photograph of the patient demonstrating a spontaneous right head tilt. The patient's head is tilted toward his right shoulder to suppress his diplopia Figure 2 : Ocular movements : There is a left hypertropia in primary position; the hypertropia was worse in right gaze Figure 3 : Lateral gazes : The left hypertropia and the diplopia were worse when the patient looked to the right Figure 4 : Lateral head tilt : The left hypertropia and the diplopia were worse with left head tilt Figure 5: Fundus photographs : Conjugate torsion of both eyes with the upper pole deviated toward the hypotropic eye Figure 6: T1-weighted axial brain MRI : Multiple lesions in the posterior fossa consistent with brain metastasisMTemspoculartiltreaction, VBintracranialtumors, EECintracranialtumors, EECoculartiltreactio

    Case Reports of Peripapillary Choroidal Neovascular Membrane in 6 Patients With Intracranial Hypertension

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    We sought to describe initial features and history of patients diagnosed with peripapillary choroidal neovascularization (PCNV), a rare and challenging complication of chronic papilledema in intracranial hypertensions (IH)

    Microcystic Macular Degeneration In Autosomal Optic Neuropathy

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    Patients with autosomal optic neuropathy (AON) can develop microcystic macular degeneration (MMD). MMD has been linked to trans-synaptic retrograde degeneration or vitreo-macular traction (VMT). We aimed to investigate the prevalence of MMD and describe their relationships with retinal layers thicknesses and visual function in subjects with AON related to dominant optic atrophy or Wolfram syndrome

    Neurological findings in patients with Leber's Hereditary Optic Neuropathy

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    Extra-ocular manifestations in Leber's Hereditary Optic Neuropathy (LHON) are commonly referred to as LHON "Plus" syndrome. Neurologic anomalies, such as dystonia, peripheral neuropathy, myoclonus and myopathy have been reported in LHON and linked to specific mitochondrial mutations. We aimed to describe neurologic findings in a French cohort of patients with LHON mutations
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