Transient Loss of Vision in the Right Eye

Surgery ◽  
2015 ◽  
pp. 547-557
Author(s):  
Christian de Virgilio ◽  
Jessica Beth O’Connell ◽  
Areg Grigorian
Surgery ◽  
2019 ◽  
pp. 627-634
Author(s):  
Areg Grigorian ◽  
Jessica Beth O’Connell ◽  
Christian de Virgilio

Author(s):  
Ashish Maheshwari ◽  
Dnyaneshwar Shridharrao Patale ◽  
Trupti Lokhande ◽  
Smita Chouhan ◽  
Sana Mariyam

Neuromyelitis Optica (NMO) is a demyelinating inflammatory disorder of the spinal cord and optic nerve. As per American Society For Apheresis (ASFA) guidelines, Therapeutic Plasma Exchange (TPE) is considered as a second-line treatment in patients with weak or no response to steroid therapy. A patient of NMO presented to the tertiary care institute with a sudden loss of vision in the right eye. The patient was resistant to steroid treatment and improved significantly with TPE. Hence, TPE may be an effective treatment modality in steroid-resistant NMO with vision loss.


2022 ◽  
Vol 7 (4) ◽  
pp. 337-340
Author(s):  
Priyanshu Bansal ◽  
Vineet Sehgal ◽  
Lucky Bhalla ◽  
Shaifali Arora

COVID-19 illness is an evolving disorder, and many extrapulmonary manifestations have been reported. With this report, we are highlighting one of the neuro-ophthalmologic complications of Covid-19. We report a case of 16 years old boy who presented with complaints of rapid loss of vision and retroorbital pain in the Right eye during recovery from Covid -19 infection. Clinically, radiologically, CSF, Blood, and all other investigations suggest Probable Covid -19 Right Eye Optic Neuritis. The patient showed remarkable recovery following steroid therapy. This report aims to add a case to the limited literature available on Optic Neuritis following Covid-19 infection.


Author(s):  
Roger L. Coakes ◽  
Patrick J. Holmes Sellors

Heart ◽  
2011 ◽  
Vol 97 (Suppl 1) ◽  
pp. A82-A83
Author(s):  
A. E. Bewick ◽  
A. Gasson ◽  
L. Ala ◽  
R. A. Bleasdale

2021 ◽  
Vol 11 (9) ◽  
pp. 1215
Author(s):  
Erwan David ◽  
Julia Beitner ◽  
Melissa Le-Hoa Võ

We wish to make the following correction to the published paper “Effects of Transient Loss of Vision on Head and Eye Movements during Visual Search in a Virtual Environment” [...]


Author(s):  
Himanshu Narula ◽  
Suneeta Meena ◽  
Sweta Jha ◽  
Neelam Kaistha ◽  
Monika Pathania ◽  
...  

Background and Purpose: Rhinocerebral mycosis is a rapidly invasive infection in diabetic patients with an unfavorable course. Herein, we report a rare case of orbital cellulitis caused by Curvularia lunata following fungal rhinosinusitis in a diabetic male patient. Case report: A 35-year-old male with uncontrolled diabetes presented to the emergency department of our center with high-grade fever accompanied by chills and rigors, severe diffuse headache, and projectile vomiting with swelling and loss of vision in the right eye. The tissue sample from surgical debridement showed pigmented hyphae; in addition, Curvularia lunata was isolated in culture. Imaging was indicative of orbital extension. Therefore, the patient was diagnosed with fungal rhinosinusitis with orbital cellulitis. The patient was subjected to extensive surgical debridement, along with antifungals. Rhinosinusitis resolved; however, the loss of vision was irreversible. Conclusion: Orbital cellulitis is a very rare but life-threatening complication of fungal rhinosinusitis. Very few cases of orbital cellulitis following fungal rhinosinusitis have been reported in the literature. Early and prompt diagnosis can save the life of a patient.


2021 ◽  
pp. 716-723
Author(s):  
Pitirat Panpruang ◽  
Monton Wongwandee ◽  
Nattapun Rattanajaruskul ◽  
Worawut Roongsangmanoon ◽  
Arthit Wongsoasu ◽  
...  

Alice in Wonderland syndrome (AIWS) is a rarely curious visual perceptual disorder which has been associated with diverse neurologic and psychiatric problems. It may be a manifestation in migraine, epileptic seizures, encephalitis, other brain lesions, medication-related side effects, schizophrenia, and depressive disorders. Principal character of AIWS is the disproportion between the external world and the self-image in which micropsia (objects appear smaller), macropsia (objects appear larger), and teleopsia (objects appear further away) are frequently reported. The cases of temporal lobe epilepsy may present with complex visual auras of visual distortions (e.g., micropsia and macropsia) like AIWS. We report an unusual case of an elderly man who presented with AIWS, focal impaired awareness seizures, ictal tachyarrhythmia, multiple episodes of transient visual disturbances of macropsia and transient loss of consciousness. During those symptoms, telemetry showed self-limited supraventricular tachycardia several times which could not be regulated with heart rate-controlled medication. The electroencephalography was later tested and showed rhythmic theta activity over the right cerebral hemisphere. He was treated with levetiracetam, and all his symptoms and tachyarrhythmias were gradually resolved thereafter. Refractory response to treatment would remind the physicians to reassess for the correct diagnosis.


2020 ◽  
pp. 106-130
Author(s):  
Louis R. Caplan

Abstract: This chapter describes Fisher’s career in Montreal (1950–1954) and his ultimate transfer to Boston. His family life, studies, accomplishments, and writings during this period are also described. Highlighted are his discoveries about carotid artery disease, transient loss of vision, transient episodes of brain ischemia, lacunar brain infarction and its mechanisms, brain embolism, and the distribution of atherosclerosis within the arteries that supply the brain. While in Montreal, Fisher became a productive researcher. His work on carotid artery disease and temporary episodes of eye and brain ischemia gained him widespread recognition. However, he eventually decided that the future of his stroke work was far brighter in Boston than if he stayed in Montreal, and so he eventually decided to return to Boston.


2021 ◽  
Vol 14 (7) ◽  
pp. e243267
Author(s):  
Abhinav Kumar ◽  
Vijay Pothula

This is the case of a parameningeal alveolar rhabdomyosarcoma (ARMS) in a 13-year-old boy who presented with painless loss of vision in the right eye, but very few other physical signs. The ARMS diagnosis was confirmed with imaging and molecular characterisation of the tumour. Despite tolerating the initial chemotherapy and radiotherapy regimens, there was leptomeningeal recurrence and the patient unfortunately passed away. Parameningeal ARMS occurs in an area of the body, which leads to a wide variety of possible presenting symptoms, creating a long list of differentials that can delay treatment. This tumour subtype has a poor prognosis, and due to the location of the tumour around vital structures in the head, treatment toxicities must be taken into account. This highlights the necessity for having a strong index of suspicion for this tumour in atypical presentations in children, and the necessity for prompt treatment to prevent leptomeningeal disease from occurring.


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